var efo_names = {"Pasteurella hemorrhagic septicemia": "EFO:1001091", "Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome": "Orphanet:363523", "endomyocardial fibrosis": "EFO:1000921", "cardinal system": "UBERON:2000096", "T-helper 2 cell": "CL:0000546", "plant ovary {http": "PO:0009072", "17alpha-ethynylestradiol": "CHEBI:4903", "Autosomal dominant spastic paraplegia type 8": "Orphanet:100989", "Hyper-IgM syndrome type 3": "Orphanet:101090", "2-oxobutanoate {http": "CHEBI:16763", "COV644": "EFO:0006386", "Bladder Flat Intraepithelial Lesion": "EFO:1000126", "Nucella lapillus": "NCBITaxon:51631", "2 formation of axillary shoot stage {http": "PO:0007073", "Distal trisomy 3p": "Orphanet:96071", "Cyanothece": "NCBITaxon:43988", "Human adenovirus 5": "NCBITaxon:28285", "dyslexia": "EFO:0005424", "Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation": "Orphanet:93222", "pharyngula prim-25": "EFO:0001313", "neurotic excoriation": "EFO:1000741", "hypothalamic neoplasm": "EFO:1000979", "Fallopian Tube Serous Adenocarcinoma": "EFO:1000253", "3-hydroxybutyrylcarnitine {http": "CHEBI:72995", "PC-6": "EFO:0002845", "Megalocornea {http": "HP:0000485", "arachidonic acid": "CHEBI:15843", "Bubalus bubalis": "NCBITaxon:89462", "CD4-negative, CD8-negative type I NK T cell secreting interleukin-4": "CL:0000930", "CHAOS measure": "EFO:0004779", "5637": "EFO:0002096", "Excretory apparatus of the lacrimal system anomaly": "Orphanet:98605", "Autosomal recessive spastic paraplegia type 7": "Orphanet:99013", "oropharynx cancer": "EFO:1001931", "Theiler stage 2": "EFO:0004394", "Golgi apparatus": "GO:0005794", "Multiple endocrine neoplasia": "Orphanet:276161", "Speech apraxia {http": "HP:0011098", "DEND syndrome": "Orphanet:79134", "response to camptothecin": "GO:1901563", "Autosomal recessive spastic paraplegia type 66": "Orphanet:401815", "HCC15": "EFO:0003129", "duodenal obstruction": "EFO:1000908", "L lactate dehydrogenase measurement": "EFO:0004808", "Hypothalamic hamartomas with gelastic seizures": "Orphanet:86906", "Autoinflammatory syndrome with immune deficiency": "Orphanet:290839", "repiratory basal cell": "CL:0002633", "Ambystoma mexicanum": "NCBITaxon:8296", "Duplication of the esophagus": "Orphanet:91357", "cell property": "EFO:0000323", "Klatskin's tumor": "EFO:1001005", "CS57834": "EFO:0000137", "Spinocerebellar ataxia type 32": "Orphanet:276183", "Salmonella": "NCBITaxon:590", "leukemia": "EFO:0000565", "hepatocyte": "CL:0000182", "Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type": "Orphanet:70472", "frozen shoulder": "EFO:1000941", "12p12.1 microdeletion syndrome": "Orphanet:313884", "seasonal gut microbiome measurement": "EFO:0007753", "Alpha-mannosidosis, adult form": "Orphanet:309288", "large intestine": "UBERON:0000059", "Distal 22q11.2 microduplication syndrome": "Orphanet:261337", "SK-MEL-30": "EFO:0006488", "quadrate": "UBERON:0006597", "vitamin D-binding protein measurement": "EFO:0005675", "LP.20 twenty or more leaves whorls visible stage": "PO:0007082", "CFPAC-1": "EFO:0006551", "Genitopatellar syndrome": "Orphanet:85201", "enrichment process": "EFO:0009090", "Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form": "Orphanet:308712", "C-peptide measurement": "EFO:0005187", "Endolymphatic Sac Tumor": "EFO:1000230", "Aniridia - ptosis - intellectual disability - familial obesity": "Orphanet:1067", "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers": "Orphanet:206546", "intersegmental vessel": "UBERON:0014907", "Autosomal recessive facio-digito-genital syndrome": "Orphanet:1974", "T-B+ severe combined immunodeficiency due to CD45 deficiency": "Orphanet:169157", "culture supernatant": "BTO:0002217", "Thyroglossal Duct Cyst": "EFO:1000585", "hemangioma of subcutaneous tissue": "EFO:1000707", "Capsella bursa-pastoris": "NCBITaxon:3719", "Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome": "Orphanet:281201", "Cerebroretinal vasculopathy": "Orphanet:3421", "monocypte percentage of leukocytes": "EFO:0007989", "Cervicothoracic spina bifida cystica": "Orphanet:268766", "454 GS FLX Titanium sequencer": "EFO:0004433", "ovalbumin": "EFO:0002674", "GM14464 {http": "CLO:0031278", "Zechi-Ceide syndrome": "Orphanet:217017", "Autosomal recessive omodysplasia": "Orphanet:93329", "respiratory disease biomarker": "EFO:0006841", "Lipodystrophy - intellectual disability - deafness": "Orphanet:50811", "Osteochondrosis": "EFO:0008575", "Parabacteroides": "NCBITaxon:375288", "liver primordium": "UBERON:0003894", "Lactobacillus delbrueckii subsp. bulgaricus ATCC BAA-365": "NCBITaxon:321956", "bacterial pneumonia": "EFO:1001272", "Pinctada maxima": "NCBITaxon:104660", "nasopharynx": "UBERON:0001728", "Acroosteolysis dominant type": "Orphanet:955", "carbohydrate sulfotransferase 15 measurement": "EFO:0008066", "Kenny-Caffey syndrome": "Orphanet:2333", "carbonic anhydrase 13 measurement": "EFO:0008067", "High myopia-sensorineural deafness syndrome": "Orphanet:363396", "Streptococcus gordonii str. Challis": "NCBITaxon:29390", "Hereditary cerebral hemorrhage with amyloidosis, Dutch type": "Orphanet:100006", "brucellosis": "EFO:0007185", "Leukoplakia, Hairy": "EFO:1001360", "46,XX disorder of sex development - anorectal anomalies": "Orphanet:2973", "Lactococcus phage c2": "NCBITaxon:31537", "A204": "EFO:0002102", "chlorosome": "GO:0046858", "GM2 gangliosidosis": "Orphanet:309152", "atrophic gastritis": "EFO:1000826", "CPC-N": "EFO:0006559", "Abnormality of zinc homeostasis": "HP:0008277", "antennal primordium2": "EFO:0000258", "HCT15": "EFO:0002188", "Vitamin B12-responsive methylmalonic acidemia type cblB": "Orphanet:79311", "PGM-CDG": "Orphanet:319646", "COG1-CDG": "Orphanet:263508", "mental retardation with language impairment": "EFO:1001500", "Ring chromosome 2": "Orphanet:96171", "environmental stress": "EFO:0000470", "cardiovascular system": "UBERON:0004535", "commensal Desulfovibrionaceae infectious disease": "EFO:1000875", "Partial duplication of chromosome 8": "Orphanet:262638", "Bronchiectasis": "HP:0002110", "Larix laricina": "NCBITaxon:3326", "X-linked intellectual disability - precocious puberty - obesity": "Orphanet:85318", "whole plant fruit formation stage": "PO:0007042", "Aldosterone-producing adenoma with seizures and neurological abnormalities": "Orphanet:369929", "Combined pituitary hormone deficiencies, genetic forms": "Orphanet:95494", "abnormal facial shape {http": "HP:0001999", "Infantile nephronophthisis": "Orphanet:93591", "otitis media with effusion": "EFO:0007415", "Arrhythmogenic right ventricular dysplasia": "Orphanet:247", "Thyroid Gland Mixed Medullary and Follicular Cell Carcinoma": "EFO:1000589", "Familial median cleft of the upper and lower lips": "Orphanet:401942", "hepatitis": "HP:0012115", "vitamin deficiency": "EFO:0005878", "Congenital dyserythropoietic anemia type I": "Orphanet:98869", "glycogen storage disease VIII": "EFO:1000952", "5-acetamido-6-formamido-3-methyluracil {http": "CHEBI:32643", "enzootic pneumonia of calves": "EFO:0007256", "fibromuscular dysplasia": "EFO:1000938", "uninfected": "EFO:0001460", "vulvar intraepithelial neoplasia": "EFO:0002627", "spine bone size": "EFO:0004508", "obesity": "EFO:0001073", "Intellectual disability, Wolff type": "Orphanet:3080", "SK-MM-2": "EFO:0005458", "hepatocellular carcinoma": "EFO:0000182", "Gastrointestinal Hamartoma": "EFO:1000280", "Perimeningeal Infections": "EFO:1001392", "Annular epidermolytic ichthyosis": "Orphanet:281139", "STA-ET-2.1": "EFO:0002863", "Smart-seq2": "EFO:0008931", "Helminthiasis": "EFO:1001342", "Genetic obesity": "Orphanet:77828", "allergic conjunctivitis": "EFO:0007141", "Severe congenital hypochromic anemia with ringed sideroblasts": "Orphanet:300298", "irradiate": "EFO:0000554", "Postia placenta": "NCBITaxon:104341", "neutrophilic promyelocyte": "CL:0000564", "commensal Bifidobacteriales infectious disease": "EFO:1000873", "lymphocyte count": "EFO:0004587", "Pseudounicornuate uterus": "Orphanet:180079", "Cricetulus griseus": "NCBITaxon:10029", "Monieziasis": "EFO:1001372", "vasculogenic impotence": "EFO:1001234", "iron accumulation in brain {http": "HP:0012675", "RIP": "EFO:0005033", "indolin-2-one {http": "CHEBI:31697", "Mosaic trisomy 14": "Orphanet:1703", "pancreatic endocrine carcinoma": "EFO:0007416", "Drosophila santomea": "NCBITaxon:129105", "Dictyostelium discoideum": "NCBITaxon:44689", "carbon dioxide treatment {http": "EO:0001020", "Chlamydia trachomatis infectious disease": "EFO:0007205", "Right temporal lobar atrophy": "Orphanet:293848", "Syndromic diarrhea": "Orphanet:84064", "partial thromboplastin time": "EFO:0004310", "pronephric mesoderm": "UBERON:0005721", "Syndrome or malformation associated with head and neck malformations": "Orphanet:156237", "GM17190 {http": "CLO:0013794", "Deafness - oligodontia": "Orphanet:3230", "Rett syndrome": "Orphanet:778", "rheumatoid factor seropositivity measurement": "EFO:0007791", "Oculocutaneous albinism type 1": "Orphanet:352731", "fC-CET": "EFO:0008739", "partial epilepsy": "EFO:0004263", "medullary thymic epithelial cell": "CL:0002365", "growth hormone-secreting pituitary adenoma": "EFO:0004125", "heart transplant rejection": "EFO:0003046", "microtubule-associated protein tau": "EFO:0005816", "estrogen receptor measurement": "EFO:0008125", "NU-DUL-1": "EFO:0006700", "urocortin I": "EFO:0002679", "FASTKD2-related infantile mitochondrial encephalomyopathy": "Orphanet:166105", "pharyngeal endoderm": "ZFA:0001104", "latitude": "OBI:0001620", "Disorder of other vitamins and cofactors metabolism and transport": "Orphanet:309833", "Kidney Medullary Carcinoma": "EFO:1000314", "autopod": "MA:0002714", "neuritic plaque measurement": "EFO:0006798", "gastrointestinal obstruction": "HP:0004796", "operator variation": "EFO:0000633", "Adenosquamous Carcinoma": "EFO:1000073", "CS57854": "EFO:0000146", "Vascular skin abnormality": "HP:0011276", "Mosaic trisomy 4": "Orphanet:96059", "arthus reaction": "EFO:1000821", "insulin": "CHEBI:5931", "operon identification design": "EFO:0001785", "growth phase culture": "BTO:0001900", "L1-S8": "EFO:0007599", "Leptosphaerulina chartarum": "NCBITaxon:55173", "Atrial tachyarrhythmia with short PR interval": "Orphanet:844", "sweetening agent role": "CHEBI:50505", "Pterygium of the conjunctiva, familial form": "Orphanet:2989", "Early infantile epileptic encephalopathy": "Orphanet:1934", "Autosomal recessive hypophosphatemic rickets": "Orphanet:289176", "response to pazopanib": "EFO:0007779", "Free sialic acid storage disease, infantile form": "Orphanet:309324", "increased rate": "PATO:0000912", "response to protease inhibitor": "EFO:0005657", "Pancreatic hypoplasia - diabetes - congenital heart disease": "Orphanet:2255", "Cortical tubers {http": "HP:0009717", "tropanyl 3,5-dimethylbenzoate": "CHEBI:64142", "Sarcomatoid Mesothelioma": "EFO:1000521", "GM17233 {http": "CLO:0014338", "Theiler stage 18": "EFO:0004408", "20p13 microdeletion syndrome": "Orphanet:313781", "root": "PO:0009005", "palmoplantar keratosis": "EFO:1000745", "Qualitative or quantitative defects of dystrophin": "Orphanet:207085", "LP.12 twelve leaves visible stage": "PO:0007064", "Muscle-eye-brain disease with bilateral multicystic leucodystrophy": "Orphanet:370997", "Congenital chloride diarrhea": "Orphanet:53689", "colorectal cancer": "EFO:0005842", "embryonic proventriculus intermediate layer": "FBbt:00005609", "Renal dysplasia": "Orphanet:93108", "alanine": "CHEBI:16449", "Disease with potential neoplastic degeneration associated with ocular features": "Orphanet:98703", "lateral cord surface glia": "FBbt:00005824", "Schistosoma japonicum": "NCBITaxon:6182", "SE.99 maximum stem length reached stage {http": "PO:0007109", "Gr1-low myeloid suppressor cell": "CL:0002468", "Developmental delay with autism spectrum disorder and gait instability": "Orphanet:329195", "Populus fremontii x Populus angustifolia": "NCBITaxon:352374", "Autosomal thrombocytopenia with normal platelets": "Orphanet:168629", "AB SOLiD 4hq System": "EFO:0004441", "fibrinogen measurement": "EFO:0004623", "Alacrimia-choreoathetosis-liver dysfunction syndrome": "Orphanet:404454", "Spondyloepimetaphyseal dysplasia with joint laxity": "Orphanet:93359", "Helicoid peripapillary chorioretinal degeneration": "Orphanet:86813", "Mytilus trossulus": "NCBITaxon:6551", "X-linked cone dysfunction syndrome with myopia": "Orphanet:90001", "Salmonella enterica subsp. enterica serovar Senftenberg": "NCBITaxon:28150", "vascular endothelial growth factor": "EFO:0003276", "kallikrein-12 measurement": "EFO:0008194", "Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia": "Orphanet:166029", "Salmonella enterica subsp. enterica serovar Typhi": "NCBITaxon:90370", "hepatitis D": "EFO:0007304", "proto-oncogene tyrosine-protein kinase receptor Ret measurement": "EFO:0008272", "immature CD11c-negative plasmacytoid dendritic cell": "CL:0000994", "IgG digalactosylation measurement": "EFO:0008424", "primary myelofibrosis": "EFO:0002430", "hereditary hemochromatosis type 1": "EFO:0006513", "x-linked ichthyosis with steryl-sulfatase deficiency": "EFO:0009080", "Situs ambiguus": "Orphanet:157769", "Xeroderma pigmentosum complementation group D": "Orphanet:276258", "flower": "PO:0009046", "L2d-dauer molt": "EFO:0005510", "NCI-H2023": "EFO:0006669", "Dysostosis with predominant craniofacial involvement": "Orphanet:93453", "Kniest dysplasia": "Orphanet:485", "Saccharomyces kudriavzevii": "NCBITaxon:114524", "Malignant Laryngeal Neoplasm": "EFO:1000354", "Vaginal Carcinosarcoma": "EFO:1000618", "mono(2-ethylhexyl) phthalate": "CHEBI:17243", "Head and Neck Paraganglioma": "EFO:1000288", "homoarginine {http": "CHEBI:24606", "band form eosinophil": "CL:0000774", "TH-1": "EFO:0002803", "blood mercury measurement": "EFO:0007580", "gingiva": "UBERON:0001828", "Qualitative or quantitative defects of calpain": "Orphanet:207104", "Marfan syndrome type 2": "Orphanet:284973", "SW48": "EFO:0002367", "Localized epidermolysis bullosa simplex": "Orphanet:79400", "brachial artery": "UBERON:0001398", "Coffin-Lowry syndrome": "Orphanet:192", "lateral shoot meristem": "EFO:0001018", "helix rolling": "EFO:0007670", "heart function measurement": "EFO:0004311", "Aortic Rupture": "EFO:1001268", "BruUV-Seq": "EFO:0008664", "neuroblastoma cell line": "EFO:0005214", "Leydig cell hypoplasia due to complete LH resistance": "Orphanet:96265", "Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type": "EFO:1000490", "clofibric acid": "CHEBI:34648", "NCI-H322T": "EFO:0006691", "Rare intellectual disability without developmental anomaly": "Orphanet:101685", "Infantile osteopetrosis with neuroaxonal dysplasia": "Orphanet:85179", "Ricinus communis": "NCBITaxon:3988", "normalization data transformation protocol": "EFO:0003816", "Double outlet right ventricle with subaortic ventricular septal defect": "Orphanet:99044", "Lactobacillus helveticus CNRZ32": "NCBITaxon:326425", "granulosa cell layer": "UBERON:0005170", "hookworm infectious disease": "EFO:0007314", "Autosomal recessive spastic paraplegia type 11": "Orphanet:2822", "Multiple Organ Failure": "EFO:1001373", "Tomato yellow leaf curl virus": "NCBITaxon:10832", "Simpson-Golabi-Behmel syndrome": "Orphanet:373", "Aedes albopictus": "NCBITaxon:7160", "response to carboplatin": "GO:0097328", "Hereditary cerebral hemorrhage with amyloidosis, Piedmont type": "Orphanet:324703", "Cy3 dye": "CHEBI:37987", "blood lead measurement": "EFO:0007040", "hyocholic acid {http": "CHEBI:81244", "Sandhoff disease, infantile form": "Orphanet:309155", "Infantile-onset ascending hereditary spastic paralysis": "Orphanet:293168", "organelle organization": "GO:0006996", "4sUDRB-seq": "EFO:0008646", "uracil {http": "CHEBI:17568", "embryonic midgut interstitial cell": "EFO:0003410", "biological process": "GO:0008150", "Vigna unguiculata subsp. unguiculata": "NCBITaxon:3920", "Streptococcus pyogenes": "NCBITaxon:1314", "Digital anomalies - intellectual disability - short stature": "Orphanet:352487", "Non-progressive cerebellar ataxia with intellectual disability": "Orphanet:314647", "Brevibacterium linens": "NCBITaxon:1703", "fetal derived definitive erythrocyte": "CL:0002357", "olfactory apparatus": "UBERON:0000004", "sympathetic nervous system": "UBERON:0000013", "Hyperprolinemia type 2": "Orphanet:79101", "Facial dysmorphism - shawl scrotum - joint laxity": "Orphanet:1778", "separation anxiety disorder": "EFO:1001916", "Adamantinoma": "Orphanet:55881", "Midline cerebral malformation": "Orphanet:268926", "Ring chromosome 9": "Orphanet:96173", "TEMPS-A questionnaire": "EFO:0004783", "Acrocephalopolydactyly": "Orphanet:221054", "NCI-H1734": "EFO:0006662", "mouse erythroleukemia cell": "EFO:0003970", "HSD10 disease": "Orphanet:391417", "Acyl-CoA dehydrogenase 9 deficiency": "Orphanet:99901", "IM95m": "EFO:0006598", "GM07022": "EFO:0001111", "Autosomal dominant osteopetrosis type 1": "Orphanet:2783", "Salmonella enterica subsp. enterica": "NCBITaxon:59201", "Wolman disease": "Orphanet:75233", "systemic lupus erythematosus": "EFO:0002690", "beta-adrenergic agonist": "CHEBI:35522", "Neolamprologus brichardi": "NCBITaxon:32507", "corpus callosum": "UBERON:0002336", "1-benzofuran": "CHEBI:35260", "Ocular albinism": "Orphanet:284804", "proliferative inflammatory atrophy": "EFO:0006893", "Meckel syndrome": "Orphanet:564", "Theiler stage 12": "EFO:0004403", "Fetal akinesia deformation sequence": "Orphanet:994", "Low anorectal malformation": "Orphanet:171215", "thyroid stimulating hormone measurement": "EFO:0004748", "embryonic foregut sensory structure": "FBbt:00005616", "DEL cells": "UBERON:2000711", "Opsoclonus-Myoclonus Syndrome": "EFO:1001383", "SR-786": "EFO:0006491", "subacute bacterial endocarditis": "EFO:1001193", "Aase-Smith syndrome": "Orphanet:916", "Prinzmetal's angina": "EFO:1000013", "oxazepam": "CHEBI:7823", "Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome": "Orphanet:363694", "M stage": "EFO:0004926", "zeaxanthin measurement": "EFO:0007896", "Pyknoachondrogenesis": "Orphanet:3003", "acute erythroleukemia": "EFO:0000218", "Frontometaphyseal dysplasia": "Orphanet:1826", "Cochleosaccular degeneration - cataract": "Orphanet:3233", "Turnip mosaic virus": "NCBITaxon:12230", "antinuclear antibody measurement": "EFO:0005949", "ovarian clear cell adenocarcinoma": "EFO:1000042", "leptospirosis": "EFO:0007344", "Classic galactosemia": "Orphanet:79239", "perceived unattractiveness to mosquitos measurement": "EFO:0008380", "response to stress": "GO:0006950", "BMI-adjusted leptin measurement": "EFO:0007793", "microtubule cytoskeleton": "GO:0015630", "Saccharomyces uvarum": "NCBITaxon:230603", "optic disc": "UBERON:0001783", "malignant lymphatic vessel tumor": "EFO:1001032", "HCS protocol": "EFO:0007570", "prodrug role": "CHEBI:50266", "Chilblain lupus": "Orphanet:90280", "Commissural facial cleft": "Orphanet:141276", "Streptococcus pyogenes MGAS6180": "NCBITaxon:319701", "Rare genetic hypothalamic or pituitary disease": "Orphanet:183628", "Rhizomelic chondrodysplasia punctata": "Orphanet:177", "Ringed hair disease": "Orphanet:169", "element": "CHEBI:33250", "Gaucher disease type 1": "Orphanet:77259", "Intellectual disability - microcephaly - phalangeal - facial abnormalities": "Orphanet:3067", "Normocalcemic tumoral calcinosis": "Orphanet:306658", "Congenital esophageal diverticulum": "Orphanet:91358", "Ring chromosome 15": "Orphanet:96177", "fertility measurement": "EFO:0006923", "Waterhouse-Friderichsen syndrome": "EFO:0007544", "Anonychia congenita totalis": "Orphanet:94150", "Partial duplication of the short arm of chromosome 1": "Orphanet:264431", "dose response design": "EFO:0001757", "leaf component": "EFO:0001983", "N-methylformamide": "CHEBI:7438", "Testicular Non-Seminomatous Germ Cell Tumor": "EFO:1000570", "Plantar Fibromatosis": "EFO:1000481", "GM14520 {http": "CLO:0031611", "Saccharomyces bayanus x Saccharomyces cerevisiae": "NCBITaxon:89981", "Sakati-Nyhan syndrome": "Orphanet:3128", "Leishmania tarentolae": "NCBITaxon:5689", "desmoplastic fibroma": "EFO:1001783", "OSC": "EFO:0005834", "G2": "EFO:0005746", "anti-CD28": "EFO:0003304", "X-linked intellectual disability, Abidi type": "Orphanet:85273", "Kaposi's sarcoma": "EFO:0000558", "hypomethylated partial restriction digest": "EFO:0004168", "stricture": "EFO:0006818", "embryonic stage 14": "EFO:0005874", "allergic rhinitis": "EFO:0005854", "urinary tract infection": "EFO:0003103", "Familial platelet syndrome with predisposition to acute myelogenous leukemia": "Orphanet:71290", "RIDDLE syndrome": "EFO:0009055", "Rare female infertility due to a congenital hypogonadotropic hypogonadism": "Orphanet:399839", "IgG plasmablast": "CL:0000982", "Autosomal dominant non-syndromic sensorineural deafness type DFNA": "Orphanet:90635", "Hypotrichosis simplex": "Orphanet:55654", "Penicillium rugulosum": "NCBITaxon:121627", "Arthrogryposis multiplex congenita": "Orphanet:1037", "Native American myopathy": "Orphanet:168572", "Isolated 3-methylcrotonyl-CoA carboxylase deficiency": "Orphanet:6", "hair morphology": "EFO:0005038", "mucosa": "UBERON:0000344", "pack-years measurement": "EFO:0006526", "intraocular pressure change measurement": "EFO:0006956", "myringosclerosis": "EFO:1001812", "osteosarcoma": "EFO:0000637", "Rare genetic tumor": "Orphanet:68336", "Yersinia enterocolitica": "NCBITaxon:630", "AZ-521": "EFO:0002814", "intracellular organelle part": "GO:0044446", "Juvenile amyotrophic lateral sclerosis": "Orphanet:300605", "Sanfilippo syndrome type B": "Orphanet:79270", "placenta accreta": "EFO:0007440", "MG63": "EFO:0002234", "topotecan": "CHEBI:63632", "CS57820": "EFO:0000129", "Pavo cristatus": "NCBITaxon:9049", "dystocia": "EFO:1000911", "compound library": "EFO:0007569", "Syndactyly type 5": "Orphanet:93406", "Lactobacillus pentosus": "NCBITaxon:1589", "hepatocellular adenoma": "EFO:0000762", "lateral nasal prominence {http": "UBERON:0004067", "Dark agouti": "EFO:0005291", "3M syndrome": "Orphanet:2616", "diazinon": "CHEBI:34682", "Polydactyly of an index finger": "Orphanet:93337", "Distal 22q11.2 microdeletion syndrome": "Orphanet:261330", "breast synovial sarcoma": "EFO:1000019", "Brachydactyly type A2": "Orphanet:93396", "Pseudohypoaldosteronism type 2D": "Orphanet:300525", "age at menopause": "EFO:0004704", "Congenital absence/hypoplasia of fingers excluding thumb": "Orphanet:294990", "Trichomegaly - cataract - hereditary spherocytosis": "Orphanet:3362", "event free survival time": "EFO:0000482", "Prochlorococcus marinus subsp. pastoris str. CCMP1986": "NCBITaxon:59919", "Primary hyperoxaluria": "Orphanet:416", "calcineurin measurement": "EFO:0008061", "Qualitative or quantitative defects of gamma-sarcoglycan": "Orphanet:207067", "protocol": "OBI:0000272", "basophil percentage of leukocytes": "EFO:0007992", "GM17160 {http": "CLO:0013984", "protein metabolic process": "GO:0019538", "Huntington disease-like 3": "Orphanet:157946", "Inguinal hernia": "HP:0000023", "Teratoma with Malignant Transformation": "EFO:1000563", "GRIL-seq": "EFO:0008754", "Streptomyces tanashiensis": "NCBITaxon:67367", "severe cutaneous adverse reaction": "EFO:0006346", "Partial trisomy/tetrasomy of chromosome 9": "Orphanet:262643", "Temple-Baraitser syndrome": "EFO:0009062", "columnar neuron": "CL:0000112", "Uniparental disomy of maternal origin": "Orphanet:98153", "phenobarbital": "CHEBI:8069", "Infantile-onset autosomal recessive nonprogressive cerebellar ataxia": "Orphanet:284332", "neutrophil collagenase measurement": "EFO:0008248", "Macrodactyly 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deficiency": "Orphanet:713", "submitter": "EFO:0001741", "Autosomal recessive lower motor neuron disease with childhood onset": "Orphanet:206580", "arsenic": "CHEBI:27563", "axial mesoderm": "UBERON:0003068", "FL.00 first flower(s) open stage": "PO:0007026", "embryonic optic lobe primordium": "UBERON:6000186", "Flaviviridae infectious disease": "EFO:0007274", "Arabidopsis suecica": "NCBITaxon:45249", "Duodenal Adenocarcinoma": "EFO:1000223", "transgenic": "EFO:0004020", "CD24-positive, CD4 single-positive thymocyte": "CL:0002432", "typhasterol": "CHEBI:27173", "sapphyrin": "CHEBI:36779", "Gastric Mucosa-Associated Lymphoid Tissue Lymphoma": "EFO:1000274", "Posterior column ataxia - retinitis pigmentosa": "Orphanet:88628", "Hereditary sensory and autonomic neuropathy type 1": "Orphanet:36386", "cardiovascular measurement": "EFO:0004298", "emotional symptom measurement": "EFO:0007803", "Mild hemophilia B": "Orphanet:169799", "geographic tongue": "EFO:0007283", "Kn-0": "EFO:0006978", "hematopoietic system": "UBERON:0002390", "ILSXISS92/TejJ": "EFO:0002998", "allergy measurement": "EFO:0007008", "visual cortex": "UBERON:0000411", "Genetic head and neck malformation": "Orphanet:183583", "Abnormality of the mandible": "HP:0000277", "event-related brain oscillation": "EFO:0004358", "(S)-1-pyrroline-5-carboxylate {http": "CHEBI:17388", "DZ685": "EFO:0005487", "indeterminate colitis": "EFO:1000034", "Pseudohypoparathyroidism type 1A": "Orphanet:79443", "GFR change measurement": "EFO:0006829", "Hepatic fibrosis - renal cysts - intellectual disability": "Orphanet:2031", "mean corpuscular volume": "EFO:0004526", "3-hydroxyhexanoate {http": "CHEBI:20070", "parotid neoplasm": "EFO:0003873", "X-linked intellectual disability - cubitus valgus - dysmorphism": "Orphanet:85280", "scalp dermatosis": "EFO:1000761", "brain": "UBERON:0000955", "LP.11 eleven leaves visible stage": "PO:0007116", "Herminiimonas arsenicoxydans": "NCBITaxon:204773", "response to water stimulus": "GO:0009415", "vitamin metabolic process": "GO:0006766", "Krukenberg Tumor": "EFO:1000316", "parental emotion expression measurmement": "EFO:0008342", "Lacrimoauriculodentodigital syndrome": "Orphanet:2363", "skeleton structure": "EFO:0003858", "trichlorofluoromethane": "CHEBI:48236", "GM17189 {http": "CLO:0013790", "sympathetic ophthalmia": "EFO:1001205", "oocyte": "CL:0000023", "synovial sarcoma": "EFO:0001376", "furosemide": "CHEBI:47426", "Desmoplastic Ameloblastoma": "EFO:1000215", "Lipedema": "Orphanet:77243", "fetal growth restriction": "EFO:0000495", "129/Sv": "EFO:0000599", "UM-UC-3": "EFO:0006771", "Fatal infantile lactic acidosis with methylmalonic aciduria": "Orphanet:17", "O-[(9Z)-tetradecenoyl]-L-carnitine {http": "CHEBI:84647", "X-linked intellectual disability - craniofacioskeletal syndrome": "Orphanet:163979", "listeriosis": "EFO:0007347", "Gerstmann syndrome": "EFO:0007285", "embryonic day 13.5": "EFO:0002564", "interleukin 2 receptor antagonist measurement": "EFO:0008332", "De Barsy syndrome": "Orphanet:2962", "primary root {http": "PO:0020127", "COLO 678": "EFO:0006371", "Wolcott-Rallison syndrome": "Orphanet:1667", "myositis": "EFO:0000783", "migraine disorder": "EFO:0003821", "Basal epidermolysis bullosa simplex": "Orphanet:158665", "choline phosphate(1-) {http": "CHEBI:295975", "Ondine syndrome": "Orphanet:661", "Autosomal dominant Charcot-Marie-Tooth disease type 2F": "Orphanet:99940", "Romano-Ward syndrome": "Orphanet:101016", "Ring chromosome 4": "Orphanet:1447", "metabolite": "EFO:0004727", "Severe combined immunodeficiency due to DNA-PKcs deficiency": "Orphanet:317425", "parotitis": "EFO:0007423", "Moynahan syndrome": "Orphanet:2574", "Rieger anomaly": "Orphanet:91483", "smooth muscle tumor": "EFO:1001185", "Gastric Small Cell Neuroendocrine Carcinoma": "EFO:1000277", "N-acetyl histidine {http": "CHEBI:86910", "childhood acute megakaryoblastic leukemia": "EFO:1001943", "chloramphenicol": "CHEBI:17698", "Abnormality of earlobe": "HP:0000363", "total cholesterol measurement": "EFO:0004574", "Alport syndrome": "Orphanet:63", "5\u00e2\u0080\u0099-GRO-seq": "EFO:0008647", "Acrodermatitis enteropathica": "Orphanet:37", "Liver Neuroendocrine Tumor": "EFO:1000325", "Ackerman syndrome": "Orphanet:2561", "Fatal multiple mitochondrial dysfunction syndrome type 2": "Orphanet:401874", "cellular protein modification process": "GO:0006464", "NOD.B10": "EFO:0002744", "family history of upper gastrointestinal cancer": "EFO:0008346", "Caldicellulosiruptor kristjanssonii": "NCBITaxon:52765", "CATCH-seq": "EFO:0008678", "intestinal epithelial cell": "CL:0002563", "SHAPE-MaP": "EFO:0008921", "Spartina maritima": "NCBITaxon:49786", "Joubert syndrome with orofaciodigital defect": "Orphanet:2754", "FL.04 end of flowering stage": "PO:0007024", "myoseptum": "UBERON:2001089", "leptin measurement": "EFO:0005000", "Miller Fisher syndrome": "EFO:0007371", "Matthew-Wood syndrome": "Orphanet:2470", "Osteopenia - myopia - hearing loss - intellectual disability - facial dysmorphism": "Orphanet:91133", "Lactobacillus helveticus DPC 4571": "NCBITaxon:405566", "Streptococcus sanguinis": "NCBITaxon:1305", "Pyogenic bacterial infections due to MyD88 deficiency": "Orphanet:183713", "overgrowth": "HP:0001548", "vagal placode 3": "UBERON:2001299", "gnathomiasis": "EFO:0007289", "Microcephaly-microcornea syndrome, Seemanova type": "Orphanet:2528", "eating disorder": "EFO:0005203", "MGAT2-CDG": "Orphanet:79329", "cerebral amyloid deposition measurement": "EFO:0007707", "Otomandibular dysplasia": "Orphanet:155896", "juvenile dermatitis herpetiformis": "EFO:1000719", "Hypospadias - hypertelorism - coloboma and deafness": "Orphanet:157788", "Neonatal hypotonia {http": "HP:0001319", "carbamoyl phosphate synthetase I deficiency disease": "EFO:0007193", "factor VII measurement": "EFO:0004619", "Lagopus lagopus scotica": "NCBITaxon:359986", "amygdala": "UBERON:0001876", "Macrocephaly - short stature - paraplegia": "Orphanet:2427", "methyltrienolone": "CHEBI:379896", "motor neuron": "CL:0000100", "3q29 microduplication": "Orphanet:251038", "neurocranial trabecula": "UBERON:0005945", "childhood cancer": "EFO:1000654", "single-organism developmental process": "GO:0044767", "shoot system {http": "PO:0009006", "Autosomal dominant Charcot-Marie-Tooth disease type 2N": "Orphanet:228174", "age at diagnosis": "EFO:0004918", "Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation": "EFO:1000593", "memory performance": "EFO:0004874", "Humulus lupulus": "NCBITaxon:3486", "Ichthyosis associated with ocular features": "Orphanet:98698", "electrically active cell": "CL:0000211", "H720": "EFO:0001166", "embryonic Malpighian tubule tip cell": "FBbt:00005643", "hepatocyte growth factor": "EFO:0003303", "dye swap quality control role": "OBI:0001142", "Severe combined immunodeficiency due to LCK deficiency": "Orphanet:280142", "Holmes-Gang syndrome": "Orphanet:93970", "Kaler-Garrity-Stern syndrome": "Orphanet:2324", "Corneoiridogoniodysgenesis": "Orphanet:98636", "CS57556": "EFO:0000014", "N0 lymph node stage": "EFO:0004932", "CAMOS syndrome": "Orphanet:83472", "clotrimazole": "CHEBI:3764", "caudate nucleus": "UBERON:0001873", "FL.02 1/2 of flowers open stage": "PO:0007053", "CB128": "EFO:0004046", "Facial onset sensory and motor neuronopathy": "Orphanet:85162", "ALG9-CDG": "Orphanet:79328", "Exercise intolerance with lactic acidosis": "Orphanet:254843", "Disorder of catecholamine synthesis": "Orphanet:309830", "presumptive neural plate": "UBERON:0007284", "triploid {http": "PATO:0001381", "Lethal occipital encephalocele-skeletal dysplasia syndrome": "Orphanet:293925", "NZO/HlLtJ": "EFO:0007729", "Actinobacillus pleuropneumoniae serovar 7": "NCBITaxon:209841", "12q15q21.1 microdeletion syndrome": "Orphanet:289513", "Partial pancreatic agenesis": "Orphanet:2805", "Tyrosinemia type 2": "Orphanet:28378", "Oculofaciocardiodental syndrome": "Orphanet:2712", "left cardiac atrium {http": "UBERON:0002079", "mammographic density percentage": "EFO:0006502", "Epidermolysis bullosa simplex with muscular dystrophy": "Orphanet:257", "skin sensitivity to sun": "EFO:0004795", "GM14432 {http": "CLO:0031238", "Isolated congenital ectropion": "Orphanet:99171", "Congenital myasthenic syndromes with glycosylation defect": "Orphanet:353327", "Spinocerebellar ataxia type 25": "Orphanet:101111", "JJN-3": "EFO:0006605", "Sickle cell disease associated with an other hemoglobin anomaly": "Orphanet:251355", "toxoplasmosis": "EFO:0007517", "AICA-ribosiduria": "Orphanet:250977", "Oculocutaneous or ocular albinism": "Orphanet:98706", "tail bud": "UBERON:0002533", "Mycoplasma gallisepticum": "NCBITaxon:2096", "Paroxysmal nocturnal hemoglobinuria": "Orphanet:447", "cochlea": "UBERON:0001844", "NCI-H1568": "EFO:0006660", "hyperparathyroidism": "EFO:0008506", "Trichoderma harzianum": "NCBITaxon:5544", "forerunner cell group": "ZFA:0000023", "Staphylococcus aureus infection": "EFO:0005681", "46,XY complete gonadal dysgenesis": "Orphanet:242", "petal differentiation and expansion stage {http": "PO:0007611", "Familial scaphocephaly syndrome, McGillivray type": "Orphanet:168624", "Ataxia - oculomotor apraxia type 1": "Orphanet:1168", "Optic neuropathy": "Orphanet:98671", "Camptodactyly syndrome, Guadalajara type 1": "Orphanet:1327", "developmental disorder of mental health": "EFO:0005548", "oncostatin M": "EFO:0003200", "basal ganglion": "UBERON:0002420", "HCC78": "EFO:0003136", "African": "EFO:0004561", "follicular dendritic cell sarcoma": "EFO:0007276", "clinical history design": "EFO:0001780", "Mitral regurgitation {http": "HP:0001653", "2-isopropylmalate {http": "CHEBI:132917", "mitochondrial DNA": "EFO:0008480", "St. Louis encephalitis": "EFO:0007495", "larval day 4": "EFO:0001304", "Partial deletion of the long arm of chromosome X": "Orphanet:263756", "Ethylmalonic encephalopathy": "Orphanet:51188", "Fine-Lubinsky syndrome": "Orphanet:1272", "Rhabdoid Tumor of the Kidney": "EFO:1000512", "dysembryoplastic neuroepithelial tumor": "EFO:0005551", "BC-1": "EFO:0002044", "GM17166 {http": "CLO:0013990", "clonorchiasis": "EFO:0007210", "Sickle cell - hemoglobin E disease": "Orphanet:251375", "Salmonella enterica": "NCBITaxon:28901", "Autosomal recessive ataxia, Beauce type": "Orphanet:88644", "intestinal epithelium": "UBERON:0001277", "X-linked severe congenital neutropenia": "Orphanet:86788", "X-linked retinal dysplasia": "Orphanet:1852", "Hydranencephaly": "Orphanet:2177", "Patella aplasia/hypoplasia, unilateral": "Orphanet:295038", "silicosis": "EFO:0007485", "luminous intensity unit": "UO:0000007", "10p11.21p12.31 microdeletion syndrome": "Orphanet:284169", "iPS-NIHi7": "EFO:0007953", "NCI-H2228": "EFO:0002284", "trigeminal placode": "UBERON:0003070", "Benign familial mesial temporal lobe epilepsy": "Orphanet:163717", "MAF": "EFO:0008791", "Pima Indian": "EFO:0003167", "anal region": "UBERON:0001353", "granuloma inguinale": "EFO:0007291", "Reducing body myopathy": "Orphanet:97239", "membrane-bounded organelle": "GO:0043227", "left superior temporal gyrus thickness measurement": "EFO:0007739", "HCC95": "EFO:0003138", "X-linked intellectual disability, Snyder type": "Orphanet:3063", "Xanthomonas {http": "NCBITaxon:338", "somite 14": "UBERON:2000726", "calcaneal bone quantitative ultrasound measurement": "EFO:0007772", "Autosomal dominant Charcot-Marie-Tooth disease type 2K": "Orphanet:99944", "Alpha-B crystallin-related late-onset distal myopathy": "Orphanet:399058", "borderline personality disorder symptom": "EFO:0005429", "nidogen-1 measurement": "EFO:0008249", "apolipoprotein B measurement": "EFO:0004615", "Retrobulbar Hemorrhage": "EFO:1001414", "mucous membrane pemphigoid": "EFO:1000680", "CSBwt-rescued fibroblasts": "EFO:0001103", "naive thymus-derived CD8-positive, alpha-beta T cell": "CL:0000900", "Geroderma osteodysplastica": "Orphanet:2078", "Familial cylindromatosis": "Orphanet:211", "Partial deletion of the long arm of chromosome 15": "Orphanet:262119", "Heart-hand syndrome type 3": "Orphanet:1342", "Otodental syndrome": "Orphanet:2791", "Mixed Tumor of the Salivary Gland": "EFO:1000384", "Spinocerebellar ataxia type 10": "Orphanet:98761", "GM17742 {http": "CLO:0017025", "trunk musculature": "UBERON:0001774", "Geobacter sulfurreducens": "NCBITaxon:35554", "Congenital muscular dystrophy type 1A": "Orphanet:258", "reading": "EFO:0005229", "MUTYH-related attenuated familial adenomatous polyposis": "Orphanet:247798", "Multiple endocrine neoplasia type 2": "Orphanet:653", "Autosomal recessive spastic paraplegia type 5A": "Orphanet:100986", "Dysostosis with predominant vertebral and costal involvement": "Orphanet:93454", "monocyte chemotactic protein 3 measurement": "EFO:0008235", "pain in abdomen": "EFO:0003766", "Enzootic Bovine Leukosis": "EFO:1001315", "Unclassified genetic skin disorder": "Orphanet:79385", "perianal Crohn's disease": "EFO:0005627", "hTERT-HM": "EFO:0005912", "CCD-11Lu": "EFO:0005360", "vehicle role": "EFO:0000732", "Illumina Genome Analyzer": "EFO:0004200", "Mowat-Wilson syndrome": "Orphanet:2152", "dermatopontin measurement": "EFO:0008108", "Neonatal epilepsy syndrome": "Orphanet:98257", "Unilateral multicystic dysplastic kidney": "Orphanet:97363", "ILSXISS114/TejJ": "EFO:0003008", "Lafora disease": "Orphanet:501", "Gingival bleeding": "HP:0000225", "hydroxyurea": "CHEBI:44423", "rat cell line": "EFO:0002936", "Benign familial chorea": "Orphanet:1429", "HCC0089": "EFO:0006419", "Inherited cancer-predisposing syndrome": "Orphanet:140162", "scChIP-seq": "EFO:0008906", "N-carbamoyl-beta-alanine {http": "CHEBI:18261", "Campylobacter jejuni subsp. jejuni NCTC 11168": "NCBITaxon:192222", "extraembryonic tissue": "UBERON:0005292", "poliomyelitis": "EFO:0007450", "Spinocerebellar ataxia type 3": "Orphanet:98757", "danazol": "CHEBI:4315", "response to montelukast": "EFO:0007612", "heart right ventricle": "UBERON:0002080", "oophoritis": "EFO:1001071", "Partial trisomy of the long arm of chromosome 18": "Orphanet:262977", "Partial deletion of the long arm of chromosome 11": "Orphanet:262092", "Staphylococcus aureus subsp. aureus N315": "NCBITaxon:158879", "Hyperlipoproteinemia type 5": "Orphanet:70470", "Recessive aplasia cutis congenita of limbs": "Orphanet:1115", "TpTe measurement": "EFO:0008334", "MiGS": "EFO:0008811", "Autosomal dominant cerebellar ataxia, deafness and narcolepsy": "Orphanet:314404", "Central Nervous System Helminthiasis": "EFO:1001773", "lateral root {http": "PO:0020121", "Nuclear oculomotor paralysis": "Orphanet:100932", "lysine measurement": "EFO:0005002", "indole-3-carboxylic acid {http": "CHEBI:24809", "embryonic stem cell": "CL:0002322", "secondary high content screen": "EFO:0007557", "Usher syndrome type 1": "Orphanet:231169", "Ascomycota": "NCBITaxon:4890", "Lilium longiflorum": "NCBITaxon:4690", "radicle emergence": "PO:0007015", "embryonal carcinoma cell": "EFO:0004987", "Non-acquired isolated growth hormone deficiency": "Orphanet:631", "Gibberella fujikuroi": "NCBITaxon:5127", "Non-epidermolytic palmoplantar keratoderma": "Orphanet:2337", "cell periphery": "GO:0071944", "Hypertriglyceridemia": "EFO:0004211", "Van den Ende-Gupta syndrome": "Orphanet:2460", "Chlorocebus sabaeus": "NCBITaxon:60711", "Dehalococcoides ethenogenes 195": "NCBITaxon:243164", "Congenital disorder of glycosylation with cardiac malformation as a major feature": "Orphanet:371183", "Methylmalonic acidemia with homocystinuria, type cblD": "Orphanet:79283", "GM17177 {http": "CLO:0014037", "Granulibacter bethesdensis": "NCBITaxon:364410", "Epidermolysis bullosa simplex with anodontia/hypodontia": "Orphanet:2325", "Vgamma5-negative CD8alpha alpha positive gamma-delta intraepithelial T cell": "CL:0002514", "metabolite measurement": "EFO:0004725", "Atelosteogenesis type I": "Orphanet:1190", "degree fahrenheit": "UO:0000195", "Congenital muscular dystrophy - infantile cataract - hypogonadism": "Orphanet:1875", "Sanfilippo syndrome type C": "Orphanet:79271", "OVCA432": "EFO:0006722", "mitochondrial part": "GO:0044429", "male infertility": "EFO:0004248", "Autosomal dominant spastic paraplegia type 42": "Orphanet:171863", "Mayer-Rokitansky-K\u00c3\u00bcster-Hauser syndrome": "Orphanet:3109", "CINCA syndrome without NLRP3 mutations": "Orphanet:93367", "Vitamin B3 deficiency": "EFO:0008570", "chronic rhinosinusitis with nasal polyps": "EFO:1002029", "Genetic neurovascular malformation": "Orphanet:371436", "Polyneuropathy - intellectual disability - acromicria - premature menopause": "Orphanet:2928", "3'-amino-3'-deoxy-N(6),N(6)-dimethyladenosine": "CHEBI:42839", "enclosing embryo Ce": "EFO:0005505", "scurvy": "EFO:1001169", "creatine": "CHEBI:16919", "post operative nausea and vomiting": "EFO:0004888", "Drosophila teissieri": "NCBITaxon:7243", "NOF151": "EFO:0006699", "Benign occipital epilepsy": "Orphanet:25968", "Adenine phosphoribosyltransferase deficiency": "Orphanet:976", "Toledo": "EFO:0002383", "whole plant {http": "PO:0000003", "intracellular organelle": "GO:0043229", "Oreochromis niloticus": "NCBITaxon:8128", "HCC4017": "EFO:0006437", "sparganosis": "EFO:0007488", "4-hydroxybenzoate {http": "CHEBI:17879", "Skeletal dysplasia - intellectual disability": "Orphanet:1436", "Partial duplication of the long arm of chromosome 8": "Orphanet:262896", "Resistance to thyrotropin-releasing hormone syndrome": "Orphanet:99832", "urinary albumin to creatinine ratio": "EFO:0007778", "Premature chromosome condensation with microcephaly and intellectual disability": "Orphanet:52183", "cell activation": "GO:0001775", "Colorectal Sessile Serrated Adenoma/Polyp": "EFO:1000197", "Pseudoleprechaunism syndrome, Patterson type": "Orphanet:2976", "susceptibility to vaginal yeast infection measurement": "EFO:0008412", "Phakomatosis pigmentokeratotica": "Orphanet:2874", "Hereditary palmoplantar keratoderma, Gamborg-Nielsen type": "Orphanet:86923", "middle lateral line neuromast": "UBERON:2000939", "Lilium regale": "NCBITaxon:82328", "embryonic central brain mushroom body": "FBbt:00005508", "Cercocebus atys": "NCBITaxon:9531", "GM17810 {http": "CLO:0016502", "GM17776 {http": "CLO:0016636", "BOR syndrome": "Orphanet:107", "Tetragametic chimerism": "Orphanet:199310", "allergic urticaria": "EFO:1000669", "spinal cord": "UBERON:0002240", "TAIL-seq": "EFO:0008960", "tongue": "UBERON:0001723", "foot": "UBERON:0002387", "hemorrhage": "MP:0001914", "sleep duration": "EFO:0005271", "kidney stone": "EFO:0003845", "Richieri Costa-da Silva syndrome": "Orphanet:3101", "Pearson syndrome": "Orphanet:699", "Spinocerebellar ataxia with oculomotor anomaly": "Orphanet:98693", "Junctional epidermolysis bullosa, Herlitz type": "Orphanet:79404", "fibronectin fragment 3 measurement": "EFO:0008131", "craniofacial tissue": "EFO:0000792", "Testicular Germ Cell Tumor": "EFO:1000566", "Brachyolmia-amelogenesis imperfecta syndrome": "Orphanet:2899", "Abnormality of cardiovascular system morphology {http": "HP:0030680", "campestanol": "CHEBI:36799", "transitional cell carcinoma of kidney": "EFO:0003017", "vascular dementia": "EFO:0004718", "Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement": "Orphanet:352306", "ATR-X-related syndrome": "Orphanet:263355", "Keloid": "EFO:0004212", "Xeroderma pigmentosum complementation group E": "Orphanet:276261", "Brachydactyly type A1": "Orphanet:93388", "Neural tube defect": "Orphanet:3388", "kallistatin measurement": "EFO:0008196", "lingual thyroid": "EFO:1001803", "abnormality of the skeletal system": "HP:0000924", "3q27.3 microdeletion syndrome": "Orphanet:397695", "month": "UO:0000035", "Duchenne muscular dystrophy": "Orphanet:98896", "Alpha-1-antitrypsin deficiency": "Orphanet:60", "Helicobacter pylori 26695": "NCBITaxon:85962", "complement component C8 measurement": "EFO:0008094", "Progressive familial intrahepatic cholestasis type 3": "Orphanet:79305", "Distal monosomy 17q": "Orphanet:1597", "DN4 thymocyte": "CL:0000808", "Crandall syndrome": "Orphanet:202", "Progressive supranuclear palsy": "Orphanet:683", "Hereditary hemorrhagic telangiectasia": "Orphanet:774", "mature Vgamma2-positive thymocyte": "CL:0002407", "Adenomatoid Odontogenic Tumor": "EFO:1000072", "dihydroferulic acid {http": "CHEBI:86612", "Neurofibromatosis type 2": "Orphanet:637", "type II NK T cell secreting interferon-gamma": "CL:0000932", "Alexander disease type I": "Orphanet:363717", "Okamoto syndrome": "Orphanet:2729", "p-value": "OBI:0001442", "Pseudomonas aeruginosa PA14 infection": "EFO:0001078", "radial nerve lesion": "EFO:1001143", "Dilated cardiomyopathy - hypergonadotropic hypogonadism": "Orphanet:2229", "Streptococcus suis 05ZYH33": "NCBITaxon:391295", "Arthrogryposis with oculomotor limitation and electroretinal anomalies": "Orphanet:1154", "ectocervix": "UBERON:0012249", "cortical thickness": "EFO:0004840", "DR1572": "EFO:0004086", "Lactobacillus rhamnosus": "NCBITaxon:47715", "eosinophilic pneumonia": "EFO:0007257", "Congenital achiasma": "Orphanet:324353", "Tc2 cell": "CL:0000918", "Goodpasture syndrome": "EFO:0007290", "Klebsiella pneumoniae": "NCBITaxon:573", "Brucella melitensis": "NCBITaxon:29459", "GM12249": "EFO:0001146", "Partial prune belly syndrome": "Orphanet:93178", "omeprazole": "CHEBI:7772", "Neu-Laxova syndrome": "Orphanet:2671", "Metaplastic Meningioma": "EFO:1000375", "HCC2885": "EFO:0006434", "hypoalbuminemia": "HP:0003073", "Rosa hybrid cultivar": "NCBITaxon:128735", "adult T acute lymphoblastic leukemia": "EFO:1001936", "CHILD syndrome": "Orphanet:139", "SBC-5": "EFO:0002855", "primary ovarian insufficiency": "EFO:0004266", "Kleine-Levin Syndrome": "EFO:1001354", "CM7-1": "EFO:0002820", "proerythroblast": "CL:0000547", "Aegilops tauschii x Triticum turgidum": "NCBITaxon:285950", "orthochromatic erythroblast": "CL:0000552", "Aromatase deficiency": "Orphanet:91", "G121": "EFO:0006399", "Trypanosoma brucei gambiense": "NCBITaxon:31285", "lymphoid MHC-II-negative classical monocyte": "CL:0002474", "Cervical Small Cell Carcinoma": "EFO:1000171", "Smith-Fineman-Myers syndrome": "Orphanet:93974", "pulmonary artery-aorta diameter ratio measurement": "EFO:0006348", "Joubert syndrome with ocular defect": "Orphanet:220493", "carotid artery intima media thickness": "EFO:0007117", "Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency": "Orphanet:319581", "temporomandibular joint disorder": "EFO:0005279", "Lowe-Kohn-Cohen syndrome": "Orphanet:2408", "Cestode Infections": "EFO:1001287", "time unit": "UO:0000003", "Corynebacterium glutamicum": "NCBITaxon:1718", "Congenital sucrase-isomaltase deficiency with starch intolerance": "Orphanet:306436", "clcn4-related disorder": "EFO:0009066", "benzoate {http": "CHEBI:16150", "Sterile multifocal osteomyelitis with periostitis and pustulosis": "Orphanet:210115", "squamous cell breast carcinoma, acantholytic variant": "EFO:1001969", "vitamin D dietary intake measurement": "EFO:0008539", "Herpetic encephalitis": "Orphanet:1930", "mansonelliasis": "EFO:0007357", "thyroid neoplasm": "EFO:0003841", "Malformation syndrome with skin/mucosae involvement": "Orphanet:139027", "S-methylcysteine {http": "CHEBI:45658", "Majeed syndrome": "Orphanet:77297", "X-linked intellectual disability, Stoll type": "Orphanet:85326", "Autosomal dominant popliteal pterygium syndrome": "Orphanet:1300", "Telecanthus - hypertelorism - strabismus - pes cavus": "Orphanet:3293", "X-linked complicated corpus callosum dysgenesis": "Orphanet:1497", "Salmonella enterica subsp. enterica serovar Montevideo": "NCBITaxon:115981", "Lennox-Gastaut syndrome": "Orphanet:2382", "hantavirus pulmonary syndrome": "EFO:0007296", "Clostridium botulinum": "NCBITaxon:1491", "aorta": "UBERON:0000947", "cytarabine": "CHEBI:28680", "Streptococcus pneumoniae TIGR4": "NCBITaxon:170187", "ATC Code J Antiinfectives for systemic use": "EFO:0005640", "Deafness - vitiligo - achalasia": "Orphanet:3239", "COLO320HSR": "EFO:0002137", "Calu6": "EFO:0002152", "Omenn syndrome": "Orphanet:39041", "suicide behaviour measurement": "EFO:0006882", "Autosomal recessive spastic paraplegia type 64": "Orphanet:401810", "screw worm infectious disease": "EFO:0007479", "Syracuse Low Avoidance": "EFO:0001347", "Prolactin-Producing Pituitary Gland Adenoma": "EFO:1000496", "MAP kinase-activated protein kinase 3 measurement": "EFO:0008226", "Partial deletion of chromosome 10": "Orphanet:261811", "Craniosynostosis, Herrmann-Opitz type": "Orphanet:2145", "cleavage 32-cell": "EFO:0001286", "HT1197": "EFO:0002202", "Granta-519": "EFO:0005369", "Optic nerve edema-splenomegaly syndrome": "Orphanet:313800", "circumcision": "EFO:0003953", "Immuno-osseous dysplasia": "Orphanet:169349", "published": "EFO:0001796", "Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments": "Orphanet:364531", "Griscelli disease type 3": "Orphanet:79478", "Genodermatosis with ocular features": "Orphanet:98696", "Capture-HiC": "EFO:0008674", "1p21.3 microdeletion syndrome": "Orphanet:293948", "cholelithiasis": "EFO:0004799", "erythroleukemia": "EFO:1001955", "Severe combined immunodeficiency due to DCLRE1C deficiency": "Orphanet:275", "S2": "EFO:0001233", "differential expression analysis data transformation": "OBI:0000650", "assay": "OBI:0000070", "Familial rhabdoid tumor": "Orphanet:231108", "Sasang constitutional medicine type": "EFO:0007119", "calcium metabolic disease": "EFO:0005769", "Landau-Kleffner syndrome": "EFO:1001010", "Qazi-Markouizos syndrome": "Orphanet:3010", "Papaver somniferum": "NCBITaxon:3469", "Leukocyte adhesion deficiency": "Orphanet:2968", "BSAS": "EFO:0008666", "hexachlorobenzene": "CHEBI:5692", "DMS 454": "EFO:0006390", "nuc-seq": "EFO:0008835", "open-angle glaucoma": "EFO:0004190", "Aquilegia formosa": "NCBITaxon:223430", "Familial benign copper deficiency": "Orphanet:1551", "body mass index": "EFO:0004340", "coated vesicle": "GO:0030135", "Diffuse palmoplantar keratoderma with painful fissures": "Orphanet:369999", "Kit-negative, Ly-76 high basophilic erythroblast": "CL:0002014", "allergic sensitization measurement": "EFO:0005298", "splenic red pulp macrophage": "CL:0000874", "Ring chromosome 13": "Orphanet:96176", "G124": "EFO:0006401", "bile duct carcinoma": "EFO:0005540", "mucosal invariant T cell": "CL:0000940", "Pentosuria": "Orphanet:2843", "Hennekam-Beemer syndrome": "Orphanet:2135", "tooth disease": "EFO:1001216", "Autosomal dominant optic atrophy, classic type": "Orphanet:98673", "2p13.2 microdeletion syndrome": "Orphanet:363680", "Palmoplantar keratoderma-esophageal carcinoma syndrome": "Orphanet:2198", "Immunoglobulin heavy chain deficiency": "Orphanet:169110", "chromium": "CHEBI:28073", "response to abiotic stimulus": "GO:0009628", "alpha-linoleic acid measurement": "EFO:0008350", "excessive daytime sleepiness measurement": "EFO:0007875", "mating type h minus": "EFO:0001269", "anterior midgut primordium": "FBbt:00000444", "inorganic gas treatment {http": "EO:0001055", "response to taxane": "EFO:0008580", "DNA repair deficiency": "EFO:0008499", "chondrocyte": "CL:0000138", "DIP-seq": "EFO:0008711", "hepcidin": "EFO:0007901", "HUES65": "EFO:0007091", "toxocariasis": "EFO:0007516", "Fraction F mature B cell": "CL:0002056", "Platyspondylic dysplasia, Torrance type": "Orphanet:85166", "Picea engelmannii x Picea glauca": "NCBITaxon:373101", "GM15038 {http": "CLO:0030309", "left": "EFO:0001658", "Pulmonic stenosis {http": "HP:0001642", "129S1/SvImJ": "EFO:0001332", "breast size": "EFO:0004884", "floor plate neural tube": "UBERON:0003306", "Sphingomonas wittichii RW1": "NCBITaxon:392499", "mast cell progenitor": "CL:0000831", "Spinal Chordoma": "EFO:1000543", "Acrocraniofacial dysostosis": "Orphanet:949", "Deeply set eye {http": "HP:0000490", "Transient infantile hypertriglyceridemia and hepatosteatosis": "Orphanet:300293", "Metabolic disease with skin involvement": "Orphanet:79387", "Schnyder corneal dystrophy": "Orphanet:98967", "interleukin-19 (Homo sapiens)": "EFO:0003801", "SNU398": "EFO:0002347", "PCSK9 protein measurement": "EFO:0006899", "NCI-H508": "EFO:0002294", "N'Dama": "EFO:0005182", "fibroblast derived cell line": "EFO:0002009", "Maternal uniparental disomy of chromosome 6": "Orphanet:96181", "ribonucleoside monophosphate metabolic process": "GO:0009161", "antisaccade response measurement": "EFO:0006874", "Autosomal ichthyosis syndrome with prominent neurologics signs": "Orphanet:281238", "functional laterality": "EFO:0003889", "deltoid": "UBERON:0001476", "radiation quantity regimen": "EO:0007153", "sex hormone-binding globulin": "EFO:0003941", "melancholia": "EFO:1002014", "Familial isolated arrhythmogenic right ventricular dysplasia": "Orphanet:217656", "hereditary thyroid gland medullary carcinoma": "EFO:1001957", "Cervical Wilms Tumor": "EFO:1000173", "Microduplication Xp11.22-p11.23 syndrome": "Orphanet:217377", "scarlet fever": "EFO:0007477", "Partial deletion of the short arm of chromosome 9": "Orphanet:261929", "Gaucher disease type 3": "Orphanet:77261", "Chinese": "EFO:0003157", "Euryblepharon": "Orphanet:99172", "Proximal spinal muscular atrophy type 4": "Orphanet:83420", "Lassa virus": "NCBITaxon:11620", "bilirubin measurement": "EFO:0004570", "Nuc-seq": "EFO:0008834", "interleukin 7 receptor subunit alpha measurement": "EFO:0008190", "DR47": "EFO:0004083", "Fibular dimelia - diplopodia": "Orphanet:1757", "NCI-H2087": "EFO:0002277", "common dendritic progenitor": "CL:0001029", "Familial isolated hyperparathyroidism": "Orphanet:99879", "uridine {http": "CHEBI:16704", "ITM-E6E7-ST": "EFO:0002063", "metopic craniosynostosis": "EFO:0008511", "Varicose veins": "HP:0002619", "CS57511": "EFO:0000002", "clozapine": "CHEBI:3766", "zebrafish cell line": "EFO:0002940", "escitalopram {http": "CHEBI:36791", "Eccrine Porocarcinoma": "EFO:1000229", "scrapie": "EFO:1001168", "HER2 Positive Breast Carcinoma": "EFO:1000294", "Familial hyperaldosteronism type I": "Orphanet:403", "Familial hyperreninemic hypoaldosteronism type 2": "Orphanet:99764", "Standard Flowgram Format (SFF)": "EFO:0004156", "BAM format": "EFO:0004157", "neutrophil count": "EFO:0004833", "Testicular Sclerosing Sertoli Cell Tumor": "EFO:1000571", "male fertility": "EFO:0004803", "fetal hemoglobin measurement": "EFO:0004576", "Streptomyces rochei": "NCBITaxon:1928", "Lymphedema - atrial septal defects - facial changes": "Orphanet:86915", "sweat gland neoplasm": "EFO:1001204", "GM15268 {http": "CLO:0027328", "Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures": "Orphanet:209341", "Bufo marinus": "NCBITaxon:8386", "Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction": "EFO:0008584", "plant anatomical entity": "PO:0025131", "myiasis": "EFO:0007389", "Melospiza melodia": "NCBITaxon:44397", "haptoglobin measurement": "EFO:0004640", "Tritanopia": "Orphanet:88629", "Ciliophora infectious disease": "EFO:0007209", "Anotia": "Orphanet:93976", "kidney derived cell line": "EFO:0001643", "deep vein thrombosis": "EFO:0003907", "isolated noncompaction of the ventricular myocardium": "EFO:1001802", "San Feliu ecotype": "EFO:0006969", "septic peritonitis": "EFO:0002623", "interferon alpha measurement": "EFO:0006517", "L-homocitrulline {http": "CHEBI:17443", "Rhodopseudomonas palustris": "NCBITaxon:1076", "Pimephales promelas": "NCBITaxon:90988", "Oscheius dolichuroides": "NCBITaxon:96645", "ethmoid cartilage": "UBERON:0011242", "Multiple keratoacanthoma, Ferguson-Smith type": "Orphanet:65748", "PK-8": "EFO:0006737", "NC37": "EFO:0002247", "Autosomal dominant hyper-IgE syndrome": "Orphanet:2314", "CORL88": "EFO:0002144", "autoimmune disease biomarker": "EFO:0006846", "Hereditary angioedema type 2": "Orphanet:100051", "Prosthesis-Related Infections": "EFO:1001406", "Total congenital cataract": "Orphanet:98994", "Nevus of Ota": "EFO:1000396", "trans-urocanate {http": "CHEBI:17771", "cancer biomarker measurement": "EFO:0005127", "simian immunodeficiency virus infection": "EFO:0001675", "basal cell carcinoma": "EFO:0004193", "Split hand - urinary anomalies - spina bifida": "Orphanet:2437", "pharyngeal pouch 4": "UBERON:0007125", "intestinal disaccharide deficiency and disaccharide malabsorption": "EFO:1000060", "cardiac embolism": "EFO:1001493", "Arthrogryposis-like syndrome": "Orphanet:1149", "Bladder Paraganglioma": "EFO:1000128", "testicular carcinoma": "EFO:0005088", "halo nevus": "EFO:1000958", "conduction system disorder": "EFO:0005137", "N-nitrosodimethylamine": "CHEBI:35807", "intercellular adhesion molecule 2 measurement": "EFO:0008163", "donor genotype effect measurement": "EFO:0007892", "eugenol": "CHEBI:4917", "GM17156 {http": "CLO:0013963", "Unverricht-Lundborg disease": "Orphanet:308", "47,XYY syndrome": "Orphanet:8", "petiole": "PO:0020038", "HCC0364": "EFO:0006420", "Developmental regression {http": "HP:0002376", "GM17852 {http": "CLO:0016449", "Vitamin B12- and folate-independent constitutional megaloblastic anemia": "Orphanet:98415", "Colonic atresia": "Orphanet:1198", "hydrophthalmos": "EFO:1000968", "Roseburia inulinivorans": "NCBITaxon:360807", "Genetic syndromic esophageal malformation": "Orphanet:371445", "Delta-beta-thalassemia": "Orphanet:231237", "Pachyonychia congenita": "Orphanet:2309", "substance unit": "UO:0000006", "Viridiplantae": "NCBITaxon:33090", "Rare disorder with hypergonadotropic hypogonadism": "Orphanet:181441", "Lactobacillus fermentum": "NCBITaxon:1613", "cranial neural crest": "UBERON:0003099", "lateral dorsal aorta": "UBERON:2001054", "diffuse scleroderma": "EFO:0000404", "Cleft palate-lateral synechia syndrome": "Orphanet:2016", "Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies": "Orphanet:370006", "KMS-12-BM": "EFO:0006612", "AMO-1": "EFO:0006534", "PWK/PhJ": "EFO:0007730", "T cell": "CL:0000084", "Recurrent infections-myelofibrosis-nephromegaly syndrome": "Orphanet:369852", "response to dabrafenib": "EFO:0007815", "Congenital contractural arachnodactyly": "Orphanet:115", "thalidomide": "CHEBI:9513", "experiment accession": "EFO:0004033", "Alymphoid cystic thymic dysgenesis": "Orphanet:169095", "Amblyomma americanum": "NCBITaxon:6943", "NUGC-2": "EFO:0006701", "T3a tumor stage": "EFO:0004941", "GM17809 {http": "CLO:0016501", "Xanthomonas oryzae pv. oryzae PXO99A": "NCBITaxon:360094", "GM18507": "EFO:0002787", "anthracosis": "EFO:1000814", "ER to Golgi transport vesicle membrane": "GO:0012507", "pyrraline {http": "CHEBI:604731", "naphthyl-keratin adduct measurement": "EFO:0004585", "fibula": "UBERON:0001446", "ganglioneuroblastoma": "EFO:0000502", "Calyptogena kilmeri gill symbiont": "NCBITaxon:72600", "Mastocytosis": "EFO:0009001", "mitochondrion": "GO:0005739", "Cataract - nephropathy - encephalopathy": "Orphanet:1380", "osteomyelitis": "EFO:0003102", "neonate": "EFO:0001372", "suppurative uveitis": "EFO:1001203", "Cerebral organic aciduria": "Orphanet:79158", "Hypotonia-cerebral atrophy-hyperglycinemia syndrome": "Orphanet:363424", "Transaldolase deficiency": "Orphanet:101028", "Wiskott-Aldrich syndrome": "Orphanet:906", "body fat percentage": "EFO:0007800", "infectious mononucleosis": "EFO:0007326", "dye swap design": "EFO:0001765", "Non-acquired pituitary hormone deficiency": "Orphanet:95488", "SF126": "EFO:0005450", "Hemolytic anemia due to diphosphoglycerate mutase deficiency": "Orphanet:714", "Hepatobiliary Neoplasm": "EFO:0008550", "Distal trisomy 16q": "Orphanet:96106", "Prenatal benign hypophosphatasia": "Orphanet:247638", "sex hormone-binding globulin measurement": "EFO:0004696", "Overhydrated hereditary stomatocytosis": "Orphanet:3203", "Dehalococcoides sp. BAV1": "NCBITaxon:216389", "hypopharynx anlage": "FBbt:00005442", "small pre-B-II cell": "CL:0000954", "lactate {http": "CHEBI:24996", "insulin response measurement": "EFO:0008473", "salivary gland body primordium": "FBbt:00005512", "Pelizaeus-Merzbacher disease, transitional form": "Orphanet:280224", "spiral organ of cochlea {http": "UBERON:0002227", "bacterial conjunctivitis": "EFO:1000829", "Gorham-Stout disease": "Orphanet:73", "Python regius": "NCBITaxon:51751", "Metabolic disease due to other fatty acid oxidation disorder": "Orphanet:309133", "uncultured organism": "NCBITaxon:155900", "response to sulfonylurea": "EFO:0007922", "Benign Brain Neoplasm": "EFO:1000107", "Poorly Differentiated Thyroid Gland Carcinoma": "EFO:1000489", "TRIBE": "EFO:0008976", "middle temporal gyrus": "UBERON:0002771", "septum of telencephalon": "UBERON:0000446", "Rare insulin-resistance syndrome": "Orphanet:181368", "dorsal fin musculature": "UBERON:2000648", "Atypical hemolytic-uremic syndrome with thrombomodulin anomaly": "Orphanet:217023", "MATQ-seq": "EFO:0008797", "Mucopolysaccharidosis type 2, attenuated form": "Orphanet:217093", "shear stressing": "EFO:0000696", "Hypophthalmichthys": "NCBITaxon:7963", "Familial hyperaldosteronism": "Orphanet:235936", "isoquinoline-1,5-diol": "CHEBI:64044", "organismal segment": "UBERON:0000914", "papillary renal cell carcinoma": "EFO:0000640", "X-linked non progressive cerebellar ataxia": "Orphanet:314978", "KELLY": "EFO:0002069", "Autosomal dominant hyperinsulinism due to Kir6.2 deficiency": "Orphanet:276580", "Peritoneal Fibrosis": "EFO:1001394", "treatment": "EFO:0000727", "ventral midline neuron": "FBbt:00005566", "ventricular fibrillation": "EFO:0004287", "Acinar Prostate Mucinous Adenocarcinoma": "EFO:1000065", "Hs 675.T": "EFO:0006587", "Bowed tibiae  - radial anomalies - osteopenia - fractures": "Orphanet:3331", "root stele": "PO:0020124", "T wave amplitude": "EFO:0008333", "Spondylometaphyseal dysplasia, Sedaghatian type": "Orphanet:93317", "blood manganese measurement": "EFO:0007581", "X-linked intellectual disability with marfanoid habitus": "Orphanet:776", "LNCaP clone FGC": "EFO:0005726", "GM15245 {http": "CLO:0027391", "Prostate Rhabdomyosarcoma": "EFO:1000498", "docosapentaenoic acid measurement": "EFO:0006809", "Primary dystonia, DYT21 type": "Orphanet:306734", "colony forming unit": "UO:0000210", "sudden infant death syndrome": "EFO:0005303", "Pyruvate carboxylase deficiency, benign type": "Orphanet:353320", "Holoprosencephaly - postaxial polydactyly": "Orphanet:2166", "N-acylethanolamine-hydrolyzing acid amidase measurement": "EFO:0008240", "Hemifacial microsomia": "Orphanet:141136", "Tuba-seq": "EFO:0008979", "Rep-Seq": "EFO:0008887", "pesticide exposure measurement": "EFO:0007840", "Dentatorubral pallidoluysian atrophy": "Orphanet:101", "lipoprotein A measurement": "EFO:0006925", "GM09579 {http": "CLO:0011438", "SW1463": "EFO:0002362", "Mus musculus musculus x M. m. domesticus": "NCBITaxon:477815", "thiostrepton": "CHEBI:29693", "presumptive paraxial mesoderm": "UBERON:0007285", "Generalized isolated dystonia": "Orphanet:376724", "intracranial volume measurement": "EFO:0004886", "Familial primary hypomagnesemia with hypocalcuria": "Orphanet:306519", "Burkholderia glumae {http": "NCBITaxon:337", "Type 2 collagen-related bone disorder": "Orphanet:93421", "Autosomal dominant spastic paraplegia type 17": "Orphanet:100998", "STS26T": "EFO:0006296", "hysterectomy": "EFO:0003881", "precentral gyrus": "UBERON:0002703", "Congenital short bowel syndrome": "Orphanet:2301", "Posterior polar cataract": "Orphanet:98993", "Isolated NADH-CoQ reductase deficiency": "Orphanet:2609", "Postaxial polydactyly type A": "Orphanet:93334", "Geospiza fortis": "NCBITaxon:48883", "CS57663": "EFO:0000056", "concentration unit": "UO:0000051", "Bm1 B cell": "CL:0000961", "GM18526": "EFO:0005348", "Methanococcoides burtonii": "NCBITaxon:29291", "methanol": "CHEBI:17790", "cardiac troponin T measurement": "EFO:0005043", "Hereditary mucoepithelial dysplasia": "Orphanet:1839", "MKN45": "EFO:0002832", "Lethal multiple pterygium syndrome": "Orphanet:33108", "Junin virus": "NCBITaxon:11619", "Omsk hemorrhagic fever virus": "NCBITaxon:12542", "analgesia requirement measurement": "EFO:0008544", "Blindness {http": "HP:0000618", "complement C1q subcomponent measurement": "EFO:0008089", "GM17197 {http": "CLO:0013818", "Deafness - epiphyseal dysplasia - short stature": "Orphanet:3218", "ILSXISS46/TejJ": "EFO:0003019", "(S)-2-hydroxyoctadecanoate {http": "CHEBI:58386", "response to trametinib": "EFO:0007816", "Exstrophy-epispadias complex": "Orphanet:322", "antipsychotic drug": "CHEBI:35476", "GM17796 {http": "CLO:0016493", "Crossed polysyndactyly": "Orphanet:2935", "gut-associated lymphoid tissue macrophage": "CL:0000885", "moderate heart failure": "EFO:0003148", "Very long chain acyl-CoA dehydrogenase deficiency": "Orphanet:26793", "DAN-G": "EFO:0006562", "Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency": "Orphanet:319589", "KS-IMM": "EFO:0002826", "Thanatophoric dysplasia type 2": "Orphanet:93274", "GR-M": "EFO:0006577", "sitting height ratio": "EFO:0007118", "vitreous body disease": "EFO:0008624", "G112": "EFO:0006396", "phosmet": "CHEBI:38786", "Hemifacial hypertrophy": "Orphanet:141145", "OCI-LY10": "EFO:0006708", "Cryptogenic late-onset epileptic spasms": "Orphanet:163708", "endothelial cell derived cell line": "EFO:0005730", "Granulomatosis with Polyangiitis": "EFO:0005297", "newly molted young adult hermaphrodite": "EFO:0005498", "pyoderma gangrenosum": "EFO:0006835", "GUIDE-seq": "EFO:0008760", "meconium aspiration syndrome": "EFO:1001037", "fungal lung infectious disease": "EFO:0007278", "vitamin transport": "GO:0051180", "CORL105": "EFO:0002141", "Epicanthal fold": "Orphanet:98573", "Holt-Oram syndrome": "Orphanet:392", "Breast Carcinoma by Gene Expression Profile": "EFO:1000143", "Mitochondrial DNA deletion syndrome with progressive myopathy": "Orphanet:352470", "stimulus or stress design": "EFO:0001762", "blastula oblong": "EFO:0001281", "WSU-NHL": "EFO:0006777", "cytoplasmic vesicle": "GO:0031410", "Familial hypocalciuric hypercalcemia type 2": "Orphanet:101049", "GM17195 {http": "CLO:0013797", "bone disease": "EFO:0004260", "Fatal familial insomnia": "Orphanet:466", "cutaneous diphtheria": "EFO:1000683", "Corneal-cerebellar syndrome": "Orphanet:3177", "Partial trisomy/tetrasomy of the short arm of chromosome 5": "Orphanet:262725", "loiasis": "EFO:1000729", "Perirhinal cortex": "UBERON:0006083", "primary Bartonellaceae infectious disease": "EFO:1001125", "GM17252 {http": "CLO:0014392", "presumptive cephalic mesoderm": "UBERON:2000414", "Closed iniencephaly": "Orphanet:268366", "renin\u00e2\u0080\u0093angiotensin\u00e2\u0080\u0093aldosterone system measurement": "EFO:0006827", "GM08398 {http": "CLO:0010526", "Colorectal Serrated Adenocarcinoma": "EFO:1000196", "disposition index measurement": "EFO:0006832", "susceptibility to scarlet fever measurement": "EFO:0008409", "drug-induced hepatitis": "EFO:1000905", "hypertensive encephalopathy": "EFO:1000976", "DNase-Seq": "EFO:0008716", "Bilateral perisylvian polymicrogyria": "Orphanet:98889", "ITM-ST": "EFO:0002064", "YCC11": "EFO:0002878", "Ehlers-Danlos syndrome type 2": "Orphanet:90318", "HCC1263": "EFO:0006424", "CD71-low, GlyA-positive polychromatic erythroblast": "CL:0002016", "CLN9 disease": "Orphanet:228357", "Hemoglobin E - beta-thalassemia": "Orphanet:231249", "ventral nerve cord primordium": "FBbt:00005554", "head capsule {http": "UBERON:0003153", "HCC1171": "EFO:0003126", "establishment of protein localization": "GO:0045184", "antineoplastic agent": "CHEBI:35610", "Fatty acid hydroxylase-associated neurodegeneration": "Orphanet:329308", "GM17217 {http": "CLO:0013887", "pericarp": "PO:0009084", "Cryptococcus neoformans var. neoformans JEC21": "NCBITaxon:214684", "fetuin-B measurement": "EFO:0008128", "Disorder of tryptophan metabolism": "Orphanet:289829", "heating block": "OBI:0400108", "Piebaldism": "Orphanet:2884", "Abelson tyrosine-protein kinase 2 measurement": "EFO:0008012", "echinocyte": "CL:0002155", "carbamazepine": "CHEBI:3387", "renal hypertension": "EFO:1002039", "Humero-ulnar synostosis, bilateral": "Orphanet:295215", "N-(1-naphthyl)ethylenediamine dihydrochloride": "CHEBI:53452", "Disorder of ornithine or proline metabolism": "Orphanet:79185", "Seizures": "HP:0001250", "Oy-0": "EFO:0006974", "S-adenosyl-L-homocysteine {http": "CHEBI:16680", "Rare genetic thyroid disease": "Orphanet:183631", "lactose intolerance": "EFO:1000062", "hyperinsulinemic hypoglycemia": "EFO:0007318", "HeLa-S3": "EFO:0002791", "Non-syndromic gastroduodenal malformation": "Orphanet:108963", "macrophage activation": "GO:0042116", "GM17206 {http": "CLO:0013833", "disease recurrence": "EFO:0004952", "peripheral neuropathy": "EFO:0003100", "Acrocallosal syndrome": "Orphanet:36", "fibroepithelial neoplasm": "EFO:0007271", "Tracheal Carcinoma": "EFO:1000599", "staphylococcal pneumonia": "EFO:0007496", "Mucopolysaccharidosis type 3": "Orphanet:581", "hormone replacement therapy": "EFO:0003961", "Rare disease with corpus callosum agenesis associated with peripheral neuropathy": "Orphanet:207031", "aneurysmal bone cyst": "EFO:1001760", "Radio-ulnar synostosis - intellectual disability - hypotonia": "Orphanet:3270", "R43": "EFO:0001228", "Buchnera sp.": "NCBITaxon:64684", "stria vascularis of cochlear duct {http": "UBERON:0002282", "Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression": "Orphanet:391316", "response to fenofibrate": "GO:1901557", "Lactobacillus salivarius": "NCBITaxon:1624", "22q11.2 microduplication syndrome": "Orphanet:1727", "Mitochondrial disease with dilated cardiomyopathy": "Orphanet:217613", "afimoxifene": "CHEBI:44616", "benzbromarone": "CHEBI:3023", "endothelium": "UBERON:0001986", "4-phenylbutyric acid": "CHEBI:41500", "Thiel-Behnke corneal dystrophy": "Orphanet:98960", "Illumina Genome Analyzer standard manufacturer's protocol": "EFO:0005082", "neuropathy": "EFO:0004149", "NCI-H2030": "EFO:0002274", "viral disease": "EFO:0000763", "ALDH18A1-related De Barsy syndrome": "Orphanet:35664", "Congenital genu flexum": "Orphanet:295232", "X-linked mixed deafness with perilymphatic gusher": "Orphanet:383", "central nervous system": "UBERON:0001017", "Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency": "Orphanet:363432", "Streptococcus agalactiae": "NCBITaxon:1311", "acute myeloblastic leukemia with maturation": "EFO:0003028", "C4I": "EFO:0002122", "5-hydroxylysine {http": "CHEBI:60175", "aflatoxin B1": "CHEBI:2504", "KBM-7": "EFO:0005903", "Kunitz-type protease inhibitor 1 measurement": "EFO:0008199", "Postaxial polydactyly of toes, bilateral": "Orphanet:295181", "ES-Bruce4 {http": "EFO:0005483", "4483": "EFO:0002809", "Aspergillus clavatus": "NCBITaxon:5057", "HydEn-seq": "EFO:0008771", "Genetic glomerular disease": "Orphanet:183586", "keratinizing squamous cell carcinoma": "EFO:0000559", "IgA plasmablast": "CL:0000984", "ornithosis": "EFO:0007410", "Medeira-Dennis-Donnai syndrome": "Orphanet:2476", "Rh deficiency syndrome": "Orphanet:71275", "potassium bromate": "CHEBI:38211", "response to cholinesterase inhibitor": "EFO:0005195", "Isolated polycystic liver disease": "Orphanet:2924", "Ataxia-telangiectasia variant": "Orphanet:370109", "ribonucleotide metabolic process": "GO:0009259", "B- and T-cell mixed leukemia": "EFO:1000828", "hypocretin deficiency": "EFO:0008323", "anxiety-like behavior": "EFO:1001877", "X-linked Alport syndrome": "Orphanet:88917", "ARPE-19": "EFO:0006271", "X-linked intellectual disability - short stature - obesity": "Orphanet:3055", "Familial dementia, British type": "Orphanet:97345", "dibutyl phthalate": "CHEBI:34687", "Familial papillary thyroid carcinoma with renal papillary neoplasia": "Orphanet:97290", "Testicular Choriocarcinoma": "EFO:1000564", "Singleton-Merten dysplasia": "Orphanet:85191", "Autosomal recessive distal osteolysis syndrome": "Orphanet:2776", "Aniridia-intellectual disability syndrome": "Orphanet:1068", "GM19193": "EFO:0005351", "Paternal 14q32.2 microdeletion syndrome": "Orphanet:254525", "rG4-seq": "EFO:0008890", "NCI-H2126": "EFO:0002280", "Autosomal anomaly": "Orphanet:98127", "GM17269 {http": "CLO:0013176", "host cell part": "GO:0033643", "Solid Pseudopapillary Neoplasm of the Pancreas": "EFO:1000542", "Androgen insensitivity syndrome": "Orphanet:754", "dodecanoate {http": "CHEBI:18262", "Ochrobactrum anthropi": "NCBITaxon:529", "Autosomal dominant distal renal tubular acidosis": "Orphanet:93608", "Locusta migratoria": "NCBITaxon:7004", "cortical thymic epithelial cell": "CL:0002364", "Genochondromatosis type 1": "Orphanet:85197", "Metatarsalgia": "EFO:1001370", "Candida tenuis": "NCBITaxon:45596", "Partial duplication of the short arm of chromosome 4": "Orphanet:262716", "Methylosinus trichosporium": "NCBITaxon:426", "GM13811 {http": "CLO:0033628", "encephalomyelitis": "EFO:0001423", "marginal zone B-cell lymphoma": "EFO:1000630", "Radial hemimelia, bilateral": "Orphanet:295071", "NCI-H69": "EFO:0002300", "Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect": "Orphanet:254519", "4-nonylphenol": "CHEBI:34440", "So-Yang": "EFO:0007121", "Combined oxidative phosphorylation defect type 9": "Orphanet:319509", "knock in expression": "EFO:0000561", "rectosigmoid adenocarcinoma": "EFO:1001966", "Clear Cell Meningioma": "EFO:1000180", "Salivary Gland Large Cell Carcinoma": "EFO:1000517", "activated CD4-positive type I NK T cell": "CL:0000925", "N-acetylglycine {http": "CHEBI:40410", "Rippling muscle disease": "Orphanet:97238", "CCL2 measurement": "EFO:0004749", "cholangiocarcinoma": "EFO:0005221", "Sj\u00c3\u00b6gren-Larsson syndrome": "Orphanet:816", "platelet count": "EFO:0004309", "behavioral response to water deprivation": "GO:0042630", "dibenzazepines": "CHEBI:47804", "Digestive System Adenoma": "EFO:1000217", "Knobloch syndrome": "Orphanet:1571", "root apical meristem": "PO:0020147", "HS-27A": "EFO:0005283", "Dermo-odonto dysplasia": "Orphanet:1660", "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency": "Orphanet:90794", "embryo leaf {http": "PO:0006338", "hypospadias": "EFO:0004209", "A172": "EFO:0002101", "thiazide-induced hyponatremia": "EFO:0008349", "DMS273": "EFO:0002164", "Amelia": "Orphanet:294925", "portion of plant tissue {http": "PO:0009007", "Brachydactyly - mesomelia - intellectual disability - heart defects": "Orphanet:1277", "interleukin 17 receptor A measurement": "EFO:0008175", "CACH syndrome": "Orphanet:135", "X-linked intellectual disability, Turner type": "Orphanet:85328", "Adrenomyeloneuropathy": "Orphanet:139399", "acid sphingomyelinase-like phosphodiesterase 3a measurement": "EFO:0008013", "silicon": "CHEBI:27573", "Microspherophakia - metaphyseal dysplasia": "Orphanet:2551", "European-American": "EFO:0003159", "methapyrilene": "CHEBI:6820", "vitreous detachment": "EFO:1001238", "GM17109 {http": "CLO:0014887", "trigeminal nerve": "UBERON:0001645", "nuclear part": "GO:0044428", "Tetrasomy 12p": "Orphanet:884", "454 Sequencing": "EFO:0005016", "Multiple intestinal atresia": "Orphanet:2300", "cortisone {http": "CHEBI:16962", "Hypotonia-speech impairment-severe cognitive delay syndrome": "Orphanet:371364", "Primary intraosseous vascular malformation": "Orphanet:140436", "osteosarcoma cell line": "BTO:0000407", "Patella aplasia/hypoplasia, bilateral": "Orphanet:295041", "toxic encephalopathy": "EFO:0005595", "Intellectual disability - dysmorphism - hypogonadism - diabetes mellitus": "Orphanet:3044", "ductal breast hyperplasia": "EFO:0008500", "Thoracolumbosacral spina bifida cystica": "Orphanet:268752", "rad": "UO:0000135", "Autosomal recessive limb-girdle muscular dystrophy type 2O": "Orphanet:206564", "regenerating fin": "ZFA:0001269", "AB SOLiD System 2.0": "EFO:0004442", "Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy": "Orphanet:217616", "Autosomal dominant limb-girdle muscular dystrophy type 1B": "Orphanet:264", "Johnson neuroectodermal syndrome": "Orphanet:2316", "diabetic angiopathy": "EFO:1000896", "YMB-1-E": "EFO:0006780", "Microform holoprosencephaly": "Orphanet:280200", "periperhal blood mesothelial cell": "CL:0002318", "infant intracranial volume measurement": "EFO:0008369", "Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins": "Orphanet:217371", "Intellectual disability - spasticity - ectrodactyly": "Orphanet:1891", "Oculo-oto-facial dysplasia": "Orphanet:77302", "Multiple pterygium syndrome": "Orphanet:294060", "Protein N6,N6,N6-trimethyl-L-lysine {http": "CHEBI:8551", "Elbow flexion contracture {http": "HP:0002987", "submandibular gland neoplasm": "EFO:1001853", "myoclonic epilepsy": "EFO:1001900", "454 GS 20 sequencer": "EFO:0004206", "age at voice drop": "EFO:0007888", "Ovarian Steroid Cell Tumor": "EFO:1000433", "Endometrial Cyst": "EFO:1000232", "786-0": "EFO:0005707", "GM17743 {http": "CLO:0017024", "HCS image acquistion and feature extraction protocol": "EFO:0007572", "Ulnar hypoplasia - split foot": "Orphanet:1122", "Hand-foot-genital syndrome": "Orphanet:2438", "soil metagenome": "NCBITaxon:410658", "Tenosynovitis": "EFO:1001435", "age at onset": "EFO:0004847", "sexually immature stage": "UBERON:0000112", "Radio-ulnar synostosis": "Orphanet:3269", "Bacillus cereus": "NCBITaxon:1396", "ZR75B": "EFO:0001264", "Ribose-seq": "EFO:0008893", "GM17762 {http": "CLO:0016600", "Combined dystonia": "Orphanet:98203", "Neuronal ceroid lipofuscinosis": "Orphanet:216", "Rorippa sylvestris": "NCBITaxon:65952", "lactic acidosis": "EFO:1000036", "vortexer": "OBI:0400118", "Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome": "Orphanet:314002", "Aegilops tauschii subsp. strangulata {http": "NCBITaxon:200361", "Cerebellar atrophy {http": "HP:0001272", "hemopneumothorax": "EFO:1000963", "Cerebellum agenesis - hydrocephaly": "Orphanet:1397", "hippocampal formation": "UBERON:0002421", "growth protocol": "EFO:0003789", "conidiophore": "BTO:0000281", "Vaccinia virus Lister": "NCBITaxon:10252", "Number of molecules": "EFO:0004368", "Classical progressive supranuclear palsy": "Orphanet:240071", "CD1c-positive myeloid dendritic cell": "CL:0002399", "Early-onset parkinsonism - intellectual disability": "Orphanet:2379", "vasomotor rhinitis": "EFO:0007533", "Acatalasemia": "Orphanet:926", "mannose": "CHEBI:37684", "hydantoin-5-propionic acid {http": "CHEBI:28297", "naive T cell": "CL:0000898", "interleukin 5 measurement": "EFO:0008185", "Autosomal recessive proximal renal tubular acidosis": "Orphanet:93607", "Hypotrichosis simplex of the scalp": "Orphanet:90368", "O-succinylcarnitine {http": "CHEBI:73034", "white matter integrity": "EFO:0004641", "risky sexual behaviour measurement": "EFO:0007877", "Microsporum distortum": "NCBITaxon:101202", "accelerated phase myeloid leukemia": "EFO:1001755", "secretory cell": "CL:0000151", "venom": "UBERON:0007113", "Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder": "Orphanet:98374", "Skull Fractures": "EFO:1001425", "Hernia of the abdominal wall": "HP:0004299", "Lepidium sativum": "NCBITaxon:33125", "Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement": "Orphanet:352312", "Dx5-negative, NK1.1-positive immature natural killer cell": "CL:0002346", "NCI-H2804": "EFO:0006688", "Gillichthys mirabilis": "NCBITaxon:8222", "46,XY disorder of sex development due to impaired androgen production": "Orphanet:325357", "CD34-positive, CD38-positive megakaryocyte erythroid progenitor cell": "CL:0002005", "Arachnodactyly - intellectual disability - dysmorphism": "Orphanet:1130", "methyltestosterone": "CHEBI:27436", "Congenital myasthenic syndromes": "Orphanet:590", "Astigmatism": "HP:0000483", "Spinocerebellar ataxia type 1 with axonal neuropathy": "Orphanet:94124", "circulatory system {http": "UBERON:0001009", "mood instability measurement": "EFO:0008475", "neuroblastoma": "EFO:0000621", "GM12812": "EFO:0001155", "iPS-5": "EFO:0007111", "Hypoalphalipoproteinemia": "Orphanet:31153", "plant growth regulator": "CHEBI:26155", "CS57890": "EFO:0000159", "Glucocorticoid resistance": "Orphanet:786", "rhinoscleroma": "EFO:0007470", "Short stature-delayed bone age due to thyroid hormone metabolism deficiency": "Orphanet:171706", "GM17754 {http": "CLO:0016558", "linoleic acid": "CHEBI:17351", "Lung Papilloma": "EFO:1000335", "scopolamine": "CHEBI:16794", "pre-B-II cell": "CL:0000955", "Sublingual Gland Neoplasms": "EFO:1001430", "Blepharophimosis - radioulnar synostosis": "Orphanet:1256", "Female infertility due to an implantation defect of genetic origin": "Orphanet:400025", "BRESEK syndrome": "Orphanet:85284", "Complete cryptophthalmia": "Orphanet:98949", "Uniparental disomy of chromosome X": "Orphanet:263793", "asparagine {http": "CHEBI:22653", "Aicardi-Gouti\u00c3\u00a8res syndrome": "Orphanet:51", "epigenetic factor": "EFO:0000472", "Familial dyskinesia and facial myokymia": "Orphanet:324588", "placental site trophoblastic tumor": "EFO:1001111", "Qualitative or quantitative defects of selenoprotein N1": "Orphanet:209193", "susceptibility to rubella infection measurement": "EFO:0008418", "Thermotoga sp. RQ2": "NCBITaxon:126740", "Dahlberg-Borer-Newcomer syndrome": "Orphanet:1563", "Familial osteochondritis dissecans": "Orphanet:251262", "diffuse idiopathic skeletal hyperostosis": "EFO:0007236", "response to doxorubicin": "GO:1902520", "prothrombin fragments F1+2 measurement": "EFO:0007776", "Ischio-vertebral syndrome": "Orphanet:85200", "Tolosa-Hunt syndrome": "Orphanet:64686", "Trichomegaly - retina pigmentary degeneration - dwarfism": "Orphanet:3363", "Arenaviridae infectious disease": "EFO:0007150", "nicotine use": "EFO:0005430", "Phosphoserine aminotransferase deficiency": "Orphanet:284417", "N-acetylcitrulline {http": "CHEBI:49006", "Homo sapiens cell line": "EFO:0002888", "diastolic blood pressure": "EFO:0006336", "San Eleno ecotype": "EFO:0005178", "hi-CLIP": "EFO:0008762", "Lethal acantholytic epidermolysis bullosa": "Orphanet:158687", "rickettsial pneumonia": "EFO:0007472", "SIRPa-negative adipose dendritic cell": "CL:0002464", "pterygium": "EFO:0000678", "Aliivibrio salmonicida LFI1238": "NCBITaxon:316275", "lipoid nephrosis": "EFO:1001020", "hypervitaminosis A": "EFO:1000978", "49,XXXXY syndrome": "Orphanet:96264", "central pontine myelinolysis": "EFO:1000857", "Joubert syndrome with hepatic defect": "Orphanet:1454", "CS57790": "EFO:0000120", "well-differentiated sarcoma": "EFO:0000737", "imprinting design": "EFO:0001747", "abnormality of the gastrointestinal tract": "HP:0011024", "hydroxymalonate(2-) {http": "CHEBI:17649", "Osteoglophonic dwarfism": "Orphanet:2645", "JVM-2 {http": "EFO:0005476", "acute megakaryoblastic leukaemia": "EFO:0003025", "strain or line design": "EFO:0001754", "ileum": "UBERON:0002116", "Velo-facial-skeletal syndrome": "Orphanet:3424", "glucosephosphate dehydrogenase deficiency": "EFO:0007287", "sevoflurane": "CHEBI:9130", "asthma exacerbation measurement": "EFO:0007614", "antennal primordium": "FBbt:00005510", "Otospondylomegaepiphyseal dysplasia": "Orphanet:1427", "peptidyl-prolyl cis-trans isomerase D measurement": "EFO:0008256", "Non-distal trisomy 9q": "Orphanet:96112", "Emericella nidulans": "NCBITaxon:162425", "thyroid carcinoma": "EFO:0002892", "24 hr schistosomulum": "EFO:0007714", "skin of body": "UBERON:0002097", "GM17738 {http": "CLO:0017023", "SC3-seq": "EFO:0008903", "colorectal adenoma": "EFO:0005406", "acetylcholinesterase inhibitor": "CHEBI:38462", "Wiedemann-Rautenstrauch syndrome": "Orphanet:3455", "folding of antihelix": "EFO:0007671", "Myelodysplastic/Myeloproliferative Neoplasm": "EFO:1000388", "decreased concentration": "PATO:0001163", "Early-onset Lafora body disease": "Orphanet:324290", "dysplasia": "EFO:0008501", "Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema": "Orphanet:2252", "Miller-Dieker syndrome": "Orphanet:531", "Myopathy and diabetes mellitus": "Orphanet:2596", "rotavirus infection": "EFO:0002622", "Vitamin B12-responsive methylmalonic acidemia": "Orphanet:28", "fibroma": "EFO:0002424", "Ameloblastic Carcinoma": "EFO:1000078", "strontium chloride": "CHEBI:36383", "2q37 microdeletion syndrome": "Orphanet:1001", "osteoarthritis, toe": "EFO:1000788", "Ralstonia solanacearum": "NCBITaxon:305", "Haemophilus influenzae R2866": "NCBITaxon:262728", "female": "PATO:0000383", "Partial deletion of chromosome 18": "Orphanet:261836", "Craniofacial-deafness-hand syndrome": "Orphanet:1529", "penile neoplasm": "EFO:1001094", "NKG2-D type II integral membrane protein measurement": "EFO:0008250", "1-hexadecanoyl-2-[(7Z,10Z,13Z,16Z)-docosatetraenoyl]-sn-glycero-3-phosphocholine {http": "CHEBI:84573", "Gonosome structural anomaly": "Orphanet:98157", "hypotaurine {http": "CHEBI:16668", "antimanic drug": "CHEBI:35477", "Li-Fraumeni syndrome": "Orphanet:524", "A101D": "EFO:0002100", "brain cancer cell line": "BTO:0000690", "acenocoumarol": "CHEBI:53766", "nephrolithiasis": "EFO:0004253", "Night blindness - skeletal anomalies - dysmorphism": "Orphanet:1390", "Colorado tick fever": "EFO:0007213", "Mietens syndrome": "Orphanet:2557", "Pseudomonas syringae pv. tomato str. DC3000": "NCBITaxon:223283", "NT2/D1": "EFO:0005236", "mutagen": "CHEBI:25435", "Aureococcus anophagefferens": "NCBITaxon:44056", "8q12 microduplication syndrome": "Orphanet:228399", "Xanthomonas axonopodis pv. citri str. 306": "NCBITaxon:190486", "C-C motif chemokine 3 measurement": "EFO:0008051", "Circumscribed cutaneous aplasia of the vertex": "Orphanet:1114", "diploid homozygous deletion library": "EFO:0007562", "Saccharomyces cerevisiae x Saccharomyces kudriavzevii": "NCBITaxon:332112", "immature dermal dendritic cell": "CL:0001009", "Zinnia violacea": "NCBITaxon:34245", "blastula 256-cell": "EFO:0001276", "CS57923": "EFO:0000165", "gametophyte": "EFO:0000988", "Lachancea": "NCBITaxon:300275", "sodium 8-bromo-3',5'-cyclic GMP": "CHEBI:64104", "Col-0": "EFO:0005148", "sciatic nerve": "UBERON:0001322", "pituitary-dependent Cushing's disease": "EFO:1001110", "IGFBP-1 measurement": "EFO:0005118", "volumetric brain MRI": "EFO:0004868", "GM17176 {http": "CLO:0014039", "interleukin 12 measurement": "EFO:0004753", "sleep depth": "EFO:0005273", "Walker-Warburg syndrome": "Orphanet:899", "phencyclidine abuse": "EFO:0007436", "uveitis": "EFO:1001231", "Hypophosphatemia": "HP:0002148", "scavenger receptor class F member 1 measurement": "EFO:0008276", "pulmonary artery": "UBERON:0002012", "LY2": "EFO:0001199", "uterine smooth muscle cell": "CL:0002601", "innate effector T cell": "CL:0002127", "3-(imidazol-5-yl)lactic acid {http": "CHEBI:27487", "cecum carcinoma": "EFO:1000021", "Synechococcus elongatus PCC 7942": "NCBITaxon:1140", "N(6)-acetimidoyl-L-lysine dihydrochloride": "CHEBI:63964", "cutaneous precancerous condition": "EFO:0006892", "Ginkgo biloba": "NCBITaxon:3311", "neuroleptic malignant syndrome": "EFO:1001379", "Acyl-CoA dehydrogenase deficiency": "Orphanet:309120", "plant embryo {http": "PO:0009009", "Spondyloenchondrodysplasia": "Orphanet:1855", "X-linked intellectual disability, Cantagrel type": "Orphanet:85277", "oesophagostomiasis": "EFO:0007400", "Central polydactyly of fingers, bilateral": "Orphanet:295173", "Pinus radiata": "NCBITaxon:3347", "thapsigargin": "CHEBI:9516", "Ataxia with vitamin E deficiency": "Orphanet:96", "Ehlers-Danlos syndrome type 7A": "Orphanet:99875", "CD4-positive type I NK T cell": "CL:0000923", "Granular corneal dystrophy type II": "Orphanet:98963", "basaloid squamous cell carcinoma": "EFO:1001940", "Short stature - wormian bones - dextrocardia": "Orphanet:2863", "L\u00c3\u00a9ri-Weill dyschondrosteosis": "Orphanet:240", "TOV-112D": "EFO:0005263", "erythema multiforme": "EFO:1000694", "Metabolic myopathy due to lactate transporter defect": "Orphanet:171690", "left ventricular structural measurement": "EFO:0008205", "Arthroderma uncinatum": "NCBITaxon:74035", "Partial deletion of the long arm of chromosome 2": "Orphanet:262010", "Distal spinal muscular atrophy type 3": "Orphanet:139547", "arthrogryposis": "EFO:0003857", "Lambert syndrome": "Orphanet:1296", "vulvar seborrheic keratosis": "EFO:1000779", "polycythemia vera": "EFO:0002429", "GT-seq": "EFO:0008758", "spotted double stranded DNA reporter": "EFO:0005076", "Hyper-IgM syndrome type 5": "Orphanet:101092", "Progressive symmetric erythrokeratodermia": "Orphanet:316", "Congenital fiber-type disproportion myopathy": "Orphanet:2020", "response to bupropion": "EFO:0006326", "MKN1": "EFO:0002830", "Nasal encephalocele": "Orphanet:141118", "response to rifampicin": "EFO:0007866", "PARS": "EFO:0008848", "Autosomal recessive limb-girdle muscular dystrophy type 2F": "Orphanet:219", "proximal portion of circumflex branch of left coronary artery": "FMA:3897", "cranium": "UBERON:0003128", "Uterine Inertia": "EFO:1001863", "EEC syndrome and related syndrome": "Orphanet:98609", "Lysosomal storage disease with skeletal involvement": "Orphanet:93448", "Dengue virus 4": "NCBITaxon:11070", "Brugia pahangi": "NCBITaxon:6280", "Bilateral polymicrogyria": "Orphanet:268940", "Wernicke encephalopathy": "EFO:1001241", "RFT1-CDG": "Orphanet:244310", "response to bortezomib": "EFO:0007808", "hybridization protocol": "EFO:0003790", "retroperitoneum": "UBERON:0003693", "salicylate {http": "CHEBI:30762", "Split hand - split foot - deafness": "Orphanet:71271", "Lethal congenital contracture syndrome type 2": "Orphanet:137776", "Pristionchus pacificus": "NCBITaxon:54126", "Recurrent infections associated with rare immunoglobulin isotypes deficiency": "Orphanet:183675", "anguloarticular": "UBERON:0004744", "childhood aggressive behaviour measurement": "EFO:0007663", "erythema nodosum": "HP:0012219", "vascular smooth muscle cell": "BTO:0004578", "Pontocerebellar hypoplasia type 8": "Orphanet:324569", "flutamide": "CHEBI:5132", "diazepam": "CHEBI:49575", "Congenital trigeminal anesthesia": "Orphanet:231013", "Macroptilium atropurpureum": "NCBITaxon:90550", "cell culture supernatant": "OBI:1000023", "Dasypus novemcinctus": "NCBITaxon:9361", "actinic keratosis": "EFO:0002496", "Congenital absence of both lower leg and foot": "Orphanet:294981", "MMEP syndrome": "Orphanet:3434", "Lactobacillus buchneri": "NCBITaxon:1581", "Noonan syndrome": "Orphanet:648", "Polydactyly of a triphalangeal thumb": "Orphanet:93336", "Partial duplication of the long arm of chromosome 14": "Orphanet:262941", "lateral line ganglion": "UBERON:2000120", "Drosophila ananassae": "NCBITaxon:7217", "Familial dysfibrinogenemia": "Orphanet:98881", "Birnaviridae Infections": "EFO:1001764", "propylparaben": "CHEBI:32063", "nervous system cell": "EFO:0002963", "CB1489": "EFO:0005491", "Abnormality of refraction": "HP:0000539", "TMK1": "EFO:0002867", "Actinobacillus pleuropneumoniae serovar 2": "NCBITaxon:34063", "Pelizaeus-Merzbacher-like disease due to HSPD1 mutation": "Orphanet:280288", "Lisch epithelial corneal dystrophy": "Orphanet:98955", "Maternally-inherited diabetes and deafness": "Orphanet:225", "myeloid lineage restricted progenitor cell": "CL:0000839", "WAGR syndrome": "Orphanet:893", "Distal limb deficiencies - micrognathia syndrome": "Orphanet:1307", "Cogan-Reese syndrome": "Orphanet:98980", "viral hemorrhagic septicemia": "EFO:0007539", "dimethylarginine {http": "CHEBI:86468", "pulpitis": "EFO:1001139", "sex cord-gonadal stromal tumor": "EFO:0007483", "distal portion of right coronary artery": "FMA:3832", "mannan-binding lectin serine protease 1 measurement": "EFO:0008223", "calvarial osteoblast": "CL:2000058", "HMEC184": "EFO:0001190", "carcinoid heart disease": "EFO:1001769", "renal glomerulus": "UBERON:0000074", "Usher syndrome type 3": "Orphanet:231183", "VIP-Producing Neuroendocrine Tumor": "EFO:1000622", "Phakomatosis pigmentovascularis": "Orphanet:2875", "GlyA-positive basophillic erythroblast": "CL:0002013", "Burkholderia Infections": "EFO:1001280", "gastrointestinal mucositis": "EFO:1001891", "Escherichia coli O157": "NCBITaxon:83334", "Genetic erythrokeratoderma": "Orphanet:183438", "Uterine Carcinosarcoma": "EFO:1000613", "protein array": "EFO:0002702", "renal system measurement": "EFO:0004742", "Deafness-infertility syndrome": "Orphanet:94064", "Progeria-associated arthropathy": "Orphanet:99706", "Partial duplication of chromosome 4": "Orphanet:262206", "1-stearoyl-sn-glycero-3-phosphoethanolamine {http": "CHEBI:83047", "Qualitative or quantitative defects of integrin alpha-7": "Orphanet:207098", "skin barrier function measurement": "EFO:0007891", "Cataract - aberrant oral frenula - growth delay": "Orphanet:1373", "Marfan syndrome type 1": "Orphanet:284963", "Dowling-Degos disease": "Orphanet:79145", "pectoral muscle": "UBERON:0001495", "Acheiria, unilateral": "Orphanet:295101", "adult": "EFO:0001272", "urticaria pigmentosa": "EFO:1001229", "Delayed gross motor development {http": "HP:0002194", "Dactylellina haptotyla": "NCBITaxon:430498", "trigeminal neuralgia": "EFO:1001219", "mating type F minus": "EFO:0004035", "Diffuse Melanocytosis": "EFO:1000216", "Parachordoma": "EFO:1000452", "1p31p32 microdeletion syndrome": "Orphanet:401986", "WW6": "EFO:0005915", "CS57630": "EFO:0000046", "X-linked epilepsy - learning disabilities - behavior disorders": "Orphanet:85294", "MJ": "EFO:0002237", "Rhabdoviridae infectious disease": "EFO:0007469", "acetone": "CHEBI:15347", "Hyper-IgM syndrome type 2": "Orphanet:101089", "Alternating hemiplegia of childhood": "Orphanet:2131", "Histone meth.": "EFO:0008764", "Hereditary geniospasm": "Orphanet:53372", "Metabolic disease with cataract": "Orphanet:98712", "IMS-MDA": "EFO:0008778", "Erythema palmaris hereditarium": "Orphanet:231031", "calcification": "EFO:0003837", "Testicular Large Cell Calcifying Sertoli Cell Tumor": "EFO:1000568", "Caplan's syndrome": "EFO:0007192", "Intellectual disability - cataracts - kyphosis": "Orphanet:171860", "chronic cystitis": "EFO:1000023", "Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form": "Orphanet:308670", "miconazole": "CHEBI:6923", "Pleuropulmonary blastoma": "EFO:0009052", "Hs 683": "EFO:0006441", "ectoderm anlage in statu nascendi": "EFO:0000435", "Rare paroxysmal movement disorder": "Orphanet:306768", "familial hypercholesterolemia": "EFO:0004911", "X chromosome number anomaly with female phenotype": "Orphanet:263717", "vastus lateralis": "UBERON:0001379", "Partial monosomy of the short arm of chromosome 17": "Orphanet:261965", "SAEC": "EFO:0002800", "Citrus sunki": "NCBITaxon:237574", "cannabis dependence": "EFO:0007191", "paraventricular organ": "UBERON:2000475", "CFT-2": "EFO:0001102", "Oromandibular-limb anomalies syndrome": "Orphanet:156215", "Anophthalmia plus syndrome": "Orphanet:1104", "Arthrogryposis - severe scoliosis": "Orphanet:65720", "AB SOLiD 5500": "EFO:0004440", "Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome": "Orphanet:397709", "Visual impairment {http": "HP:0000505", "copy number variation": "EFO:0004798", "Progressive cerebello-cerebral atrophy": "Orphanet:247198", "proximal renal artery": "EFO:0002594", "citalopram": "CHEBI:3723", "quadriceps femoris": "UBERON:0001377", "Cataract - deafness - hypogonadism": "Orphanet:1383", "Mumps virus infectious disease": "EFO:0007383", "hypersomnia": "EFO:0005246", "KYSE-180": "EFO:0006628", "embryonic day 16.5": "EFO:0002567", "major histocompatibility congenic strain": "EFO:0004011", "nickel chloride hexahydrate": "CHEBI:53542", "Oligodontia - cancer predisposition syndrome": "Orphanet:300576", "mean platelet volume": "EFO:0004584", "joint damage measurement": "EFO:0005413", "Penicillium chrysogenum": "NCBITaxon:5076", "CD38-positive naive B cell": "CL:0002101", "Spondyloepimetaphyseal dysplasia, Missouri type": "Orphanet:93356", "Legg-Calv\u00c3\u00a9-Perthes disease": "Orphanet:2380", "hyperemesis gravidarum": "EFO:1000971", "Cephalocele": "Orphanet:268817", "mental development measurement": "EFO:0008230", "response to osmotic stress": "GO:0006970", "bone fracture": "EFO:0003931", "acquired keratosis": "EFO:1000663", "spinal cord lateral wall": "UBERON:0009582", "Renal-genital-middle ear anomalies": "Orphanet:1092", "ovarian endometrioid carcinoma": "EFO:1001515", "embryonic central brain neuron": "FBbt:00005665", "dasatinib": "CHEBI:49375", "Generalized galactose epimerase deficiency": "Orphanet:308487", "Axenfeld-Rieger syndrome": "Orphanet:782", "Fast-ATAC": "EFO:0008736", "ovarian teratoma": "EFO:0006463", "Lens position anomaly": "Orphanet:98653", "peripheral vascular disease": "EFO:0003875", "Sterol biosynthesis disorder": "Orphanet:79195", "karyotype": "EFO:0004426", "connective tissue disease": "EFO:1001986", "GM14504 {http": "CLO:0031516", "monocrotaline": "CHEBI:6980", "LP.13 thirteen leaves visible stage": "PO:0007083", "beta-endorphin measurement": "EFO:0008034", "MDAMB468": "EFO:0001216", "Frontofacionasal dysplasia": "Orphanet:1791", "Madras motor neuron disease": "Orphanet:137867", "depressive symptom measurement": "EFO:0007006", "PC-10": "EFO:0002843", "Mendelian susceptibility to mycobacterial diseases": "Orphanet:748", "transitional stage B cell": "CL:0000818", "response to allopurinol": "EFO:0006337", "Autosomal dominant complex spastic paraplegia": "Orphanet:100979", "growth-regulated alpha protein measurement": "EFO:0008146", "Vicia narbonensis": "NCBITaxon:3912", "embryonic hypocerebral ganglion": "FBbt:00005669", "Keratoderma hereditarium mutilans with ichthyosis": "Orphanet:79395", "vanadyl sulfate": "CHEBI:33146", "Pseudomonas aeruginosa PAO1": "NCBITaxon:208964", "Apis dorsata": "NCBITaxon:7462", "gynoecium {http": "PO:0009062", "amebiasis": "EFO:0007144", "Congenital bile acid synthesis defect type 1": "Orphanet:79301", "Chondrodysplasia - disorder of sex development": "Orphanet:1422", "utering smooth muscle cell": "EFO:1000615", "CD27-high, CD11b-high natural killer cell": "CL:0002347", "multiple sclerosis": "EFO:0003885", "SCC-15": "EFO:0006482", "Honey-droplet corneal dystrophy": "Orphanet:98958", "CEL data file format": "EFO:0005630", "Cholesterol-ester transfer protein deficiency": "Orphanet:79506", "non-small cell lung carcinoma": "EFO:0003060", "7,12-dimethylbenz(a)anthracene": "CHEBI:254496", "KMS-34": "EFO:0006619", "Rare hyperopia and astigmatism": "Orphanet:98621", "cycloplegia": "EFO:0005758", "Familial atrial fibrillation": "Orphanet:334", "clinical laboratory measurement": "EFO:0004297", "response to acetaminophen": "GO:1901554", "rectum primordium": "FBbt:00005506", "mammalian vulva": "UBERON:0000997", "Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies": "Orphanet:221145", "Acrokeratosis verruciformis of Hopf": "Orphanet:79151", "Illumina native scarf format": "EFO:0004165", "Secondary ectropion": "Orphanet:98571", "azoxystrobin": "CHEBI:40909", "embryonic stage 6": "EFO:0005865", "amide": "EFO:0004417", "DMS114": "EFO:0002162", "ILSXISS28/TejJ": "EFO:0003018", "Acrofacial dysostosis, Catania type": "Orphanet:1786", "Apodia, unilateral": "Orphanet:295105", "alpha-beta T cell": "CL:0000789", "BJAB": "EFO:0002815", "hereditary multiple exostoses": "EFO:0005560", "HT-29": "EFO:0001193", "Rare genetic disorder with obstructive azoospermia": "Orphanet:400003", "hepatobiliary system": "UBERON:0002423", "Panicum virgatum": "NCBITaxon:38727", "Bartter syndrome with hypocalcemia": "Orphanet:263417", "Encephalocraniocutaneous lipomatosis": "Orphanet:2396", "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form": "Orphanet:315306", "GM23248": "EFO:0005723", "Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy": "Orphanet:294959", "small artery occlusion": "EFO:1001495", "Be1 Cell": "CL:0000943", "Primary hyperoxaluria type 3": "Orphanet:93600", "Congenital osteogenesis imperfecta - microcephaly - cataracts": "Orphanet:2772", "Hypocalcified amelogenesis imperfecta": "Orphanet:100032", "Tomo-Seq": "EFO:0008974", "Intellectual disability, moderate {http": "HP:0002342", "carcinoid syndrome": "EFO:1000852", "clypeo-labral primordium": "UBERON:6005538", "granulysin measurement": "EFO:0008144", "hypoblast (generic) {http": "UBERON:0000089", "total cortical area measurement": "EFO:0008381", "kynurenine {http": "CHEBI:28683", "egg allergy": "EFO:0007248", "erythroid lineage cell": "CL:0000764", "Linear and whorled nevoid hypermelanosis": "Orphanet:79150", "GM17253 {http": "CLO:0014389", "tryptophan measurement": "EFO:0008534", "gram per liter": "UO:0000175", "Ehlers-Danlos syndrome, dermatosparaxis type": "Orphanet:1901", "butan-1-ol": "CHEBI:28885", "Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism": "Orphanet:3085", "GM15223 {http": "CLO:0027483", "GM17125 {http": "CLO:0015123", "risk factor": "EFO:0003919", "Autosomal dominant isolated diffuse palmoplantar keratoderma": "Orphanet:98349", "lymphoid leukemia": "EFO:0004289", "myelocyte": "CL:0002193", "Slamf1-negative multipotent progenitor cell": "CL:0002035", "microeinstein per square meter per second": "UO:0000160", "hip fracture": "EFO:0003964", "SPARE": "EFO:0008943", "Enterococcus mundtii": "NCBITaxon:53346", "Debaryomyces hansenii": "NCBITaxon:4959", "Bacteroides": "NCBITaxon:816", "pleiotrophin": "EFO:0003172", "HES2": "EFO:0003048", "MEND syndrome": "Orphanet:401973", "smoking status measurement": "EFO:0006527", "GM15072 {http": "CLO:0030337", "response to etoposide": "GO:1902521", "Isolated growth hormone deficiency type IB": "Orphanet:231671", "undifferentiated carcinoma": "EFO:0006772", "prefrontal cortex cytoarchtiectural measurement": "EFO:0006913", "Ito hypomelanosis": "Orphanet:435", "Paroxysmal kinesigenic dyskinesia": "Orphanet:98809", "rectocele": "EFO:1001837", "Undifferentiated Pleomorphic Sarcoma, Inflammatory Variant": "EFO:1000608", "Autosomal recessive spastic paraplegia type 70": "Orphanet:401835", "Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering": "Orphanet:402003", "Salivary Gland Carcinoma ex Pleomorphic Adenoma": "EFO:1000516", "GM12870": "EFO:0005343", "Steinert myotonic dystrophy": "Orphanet:273", "Pancreatic Gastrinoma": "EFO:1000440", "Ring chromosome 22": "Orphanet:1446", "ACC112": "EFO:0007070", "Melorheostosis": "Orphanet:2485", "Huntington disease-like syndrome due to C9ORF72 expansions": "Orphanet:401901", "cancer": "EFO:0000311", "TCC": "EFO:0008965", "Humero-ulnar synostosis": "Orphanet:94056", "pancreas": "UBERON:0001264", "YAMAT-Seq": "EFO:0008987", "22q11.2 deletion syndrome": "Orphanet:567", "OCI-M1": "EFO:0006712", "Sparse hair - short stature - skin anomalies": "Orphanet:79132", "Exanthema Subitum": "EFO:1001320", "Genetic disorder of sex development of gynecological interest": "Orphanet:325665", "lipomatosis": "EFO:1000728", "angiotensinogen measurement": "EFO:0008025", "iPS-11b": "EFO:0007100", "permethrin": "CHEBI:34911", "Autosomal recessive spastic paraplegia type 30": "Orphanet:101010", "hemin": "CHEBI:50385", "platelet-derived growth factor BB measurement": "EFO:0008264", "soluble interleukin-2 receptor subunit alpha measurement": "EFO:0007650", "Autosomal recessive palmoplantar keratoderma and congenital alopecia": "Orphanet:1366", "Beta-thalassemia associated with another hemoglobin anomaly": "Orphanet:231230", "Neurofibromatosis type 1 due to NF1mutation or intragenic deletion": "Orphanet:363700", "U-251 MG": "EFO:0006498", "interleukin-6 receptor measurement": "EFO:0004814", "CARASIL": "Orphanet:199354", "Lactobacillus acidophilus": "NCBITaxon:1579", "Cerebral diseases of vascular origin with epilepsy": "Orphanet:166487", "Dehalobacter restrictus": "NCBITaxon:55583", "AHT-ChIP-Seq": "EFO:0008652", "Pectus excavatum {http": "HP:0000767", "Chuvash erythrocytosis": "Orphanet:238557", "nasal septum": "UBERON:0001706", "physical urticaria": "EFO:1000754", "octanoate {http": "CHEBI:25646", "Maternally-inherited cardiomyopathy and hearing loss": "Orphanet:1349", "Genetic multiple congenital anomalies/dysmorphic syndrome": "Orphanet:183533", "Laryngopharyngeal Reflux": "EFO:1001355", "Jejunal Neuroendocrine Tumor G1": "EFO:1000308", "TBP-105Q": "EFO:0001341", "C2BBe1": "EFO:0006546", "GM12875": "EFO:0001162", "Bietti crystalline dystrophy": "Orphanet:41751", "Livedo reticularis": "EFO:1001804", "L-2-aminobutyrate {http": "CHEBI:28340", "Clostridium sporogenes": "NCBITaxon:1509", "Toxoplasma gondii seropositivity": "EFO:0007047", "Lethal chondrodysplasia": "Orphanet:93465", "memory B cell": "CL:0000787", "PYCR1-related De Barsy syndrome": "Orphanet:293633", "Brody myopathy": "Orphanet:53347", "period of infection": "EFO:0000648", "Progressive myoclonic epilepsy type 5": "Orphanet:402082", "image": "IAO:0000101", "Syndrome with synostosis or other joint formation defect": "Orphanet:93459", "alendronic acid": "CHEBI:2567", "Intestinal malformation": "Orphanet:97945", "Genetic cardiac rhythm disease": "Orphanet:101934", "plasmablast": "CL:0000980", "Benign adult familial myoclonic epilepsy": "Orphanet:86814", "methoprene": "CHEBI:34839", "pancreatic endoderm": "EFO:0002579", "Disorder of glycerol metabolism": "Orphanet:79179", "Obesity due to melanocortin 4 receptor deficiency": "Orphanet:71529", "3-phenyllactate {http": "CHEBI:8100", "KMM-1": "EFO:0006611", "Lethal chondrodysplasia, Seller type": "Orphanet:1421", "personality trait measurement": "EFO:0007911", "anxiety": "EFO:0005230", "Congenital absence of upper arm and forearm with hand present": "Orphanet:294975", "functional decline measurement": "EFO:0007784", "Cowden syndrome": "Orphanet:201", "CD8-positive, CD25-positive, alpha-beta regulatory T cell": "CL:0000919", "AGM hematopoietic stem cell": "CL:0002360", "tethered spinal cord syndrome": "EFO:1001210", "Multiple epiphyseal dysplasia": "Orphanet:251", "Progressive myoclonic epilepsy type 3": "Orphanet:263516", "acrodermatitis chronica atrophicans": "EFO:1000665", "Symbrachydactyly of hand and foot, unilateral": "Orphanet:295136", "antidepressant-induced dizziness": "EFO:0006321", "GM14508 {http": "CLO:0031610", "putamen measurement": "EFO:0008389", "presumptive floor plate": "UBERON:0007286", "Familial renal amyloidosis due to lysozyme variant": "Orphanet:93561", "Autosomal recessive spastic paraplegia type 23": "Orphanet:101003", "eye hemorrhage": "EFO:0008627", "weight loss": "HP:0001824", "Neutral lipid storage myopathy": "Orphanet:98908", "inappropriate ADH syndrome": "EFO:1000982", "Hyaline body myopathy": "Orphanet:53698", "Pancreatic Large Cell Neuroendocrine Carcinoma": "EFO:1000442", "fructose {http": "CHEBI:28757", "Ly49CI-positive natural killer cell": "CL:0002443", "5C": "EFO:0007692", "X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency": "Orphanet:319623", "murine neuroblastoma cholinergic cell line": "EFO:0002035", "Lassa fever": "EFO:0007338", "congenital diaphragmatic hernia": "EFO:0007216", "JK1107": "EFO:0005492", "Autosomal ichthyosis syndrome": "Orphanet:281217", "controlled variable specification": "OBI:0000785", "Disorder of pyridoxine metabolism": "Orphanet:79192", "haltere": "UBERON:0000987", "anticonvulsant": "CHEBI:35623", "ulcer": "MPATH:579", "PhIP-seq": "EFO:0008861", "Epidermolysis bullosa simplex with mottled pigmentation": "Orphanet:79397", "Abnormal electroretinogram {http": "HP:0000512", "childhood supratentorial ependymoma": "EFO:0008495", "C32": "EFO:0006364", "Non-familial restrictive cardiomyopathy": "EFO:1001473", "Pure mitochondrial myopathy": "Orphanet:254854", "somite 13": "UBERON:2000975", "serum selenium measurement": "EFO:0005266", "Mediterranean macrothrombocytopenia": "Orphanet:101022", "LAPC-4": "EFO:0005392", "gastric outlet obstruction": "EFO:1000947", "Combined immunodeficiency due to MALT1 deficiency": "Orphanet:397964", "HCC227": "EFO:0005374", "Hs 852.T": "EFO:0006592", "Lethal recessive chondrodysplasia": "Orphanet:1423", "Caldicellulosiruptor hydrothermalis": "NCBITaxon:413888", "kynureninase measurement": "EFO:0008201", "myeloid cell surface antigen CD33 measurement": "EFO:0008238", "Alopecia - epilepsy - pyorrhea - intellectual disability": "Orphanet:1008", "synovitis": "EFO:0008997", "PSN1": "EFO:0006739", "RAPD": "EFO:0004167", "Trichodysplasia - amelogenesis imperfecta": "Orphanet:79129", "injury design": "EFO:0001760", "millimolar": "UO:0000063", "Senecio squalidus subsp. squalidus": "NCBITaxon:121555", "Metaphyseal anadysplasia": "Orphanet:1040", "branchiostegal ray 1": "UBERON:2001279", "weight percent by volume": "EFO:0004384", "Saccharopinuria": "Orphanet:3124", "Congenital pseudoarthrosis of the radius": "Orphanet:295024", "Bardet-Biedl syndrome 1": "EFO:0009021", "NCI-H1869": "EFO:0006664", "Familial primary localized cutaneous amyloidosis": "Orphanet:353220", "tangential nucleus": "UBERON:2000693", "Bardet-Biedl syndrome 10": "EFO:0009022", "Oculogastrointestinal muscular dystrophy": "Orphanet:1876", "KYSE-140": "EFO:0006626", "outer membrane": "GO:0019867", "Hyperphalangy, unilateral": "Orphanet:295140", "pyogenic liver abscess": "EFO:1001836", "Atypical progressive supranuclear palsy": "Orphanet:99750", "GM17811 {http": "CLO:0016499", "publication status": "EFO:0001742", "Junctional epidermolysis bullosa - pyloric atresia": "Orphanet:79403", "sphingolipid measurement": "EFO:0004622", "visceral branch primordium": "FBbt:00017003", "Theiler stage 13": "EFO:0004404", "Acral dystrophic epidermolysis bullosa": "Orphanet:158673", "HSSultan": "EFO:0002199", "Ulerythema ophryogenesis": "Orphanet:3406", "space motion sickness": "EFO:1001188", "response to diruetic": "GO:0036270", "Nebulin-related early-onset distal myopathy": "Orphanet:399103", "transcription profiling by tiling array": "EFO:0002769", "Fibulo-ulnar hypoplasia - renal anomalies": "Orphanet:2256", "cytosol": "GO:0005829", "Qualitative or quantitative defects of protein O-mannosyltransferase 2": "Orphanet:209033", "Immunodeficiency with factor I anomaly": "Orphanet:200418", "macular telangiectasia type 2": "EFO:1002009", "Syndromic urogenital tract malformation": "Orphanet:165707", "array control biosequence": "EFO:0005433", "high content analysis of cells by molecular content": "EFO:0005398", "LY294002": "CHEBI:65329", "Turner syndrome": "Orphanet:881", "Syndromic neurometabolic disease with X-linked intellectual disability": "Orphanet:182076", "GM17266 {http": "CLO:0013181", "Piriformospora indica": "NCBITaxon:65672", "Ocular albinism with late-onset sensorineural deafness": "Orphanet:1000", "Inherited ichthyosis syndromic form": "Orphanet:281085", "OVCA433": "EFO:0006723", "Partial duplication of the long arm of chromosome 22": "Orphanet:263004", "Aplasia cutis congenita - intestinal lymphangiectasia": "Orphanet:1116", "Isolated focal cortical dysplasia type IIb": "Orphanet:269008", "Pure hereditary spastic paraplegia": "Orphanet:102012", "zeugopod": "UBERON:0002471", "Petunia x hybrida": "NCBITaxon:4102", "cellular nitrogen compound biosynthetic process": "GO:0044271", "Ectodermal dysplasia - syndactyly syndrome": "Orphanet:247820", "carcinogen role": "EFO:0004457", "Magnaporthe grisea": "NCBITaxon:148305", "Bloom syndrome": "Orphanet:125", "Lactobacillus helveticus": "NCBITaxon:1587", "GM17134 {http": "CLO:0015093", "Wide intermamillary distance {http": "HP:0006610", "PD-Seq": "EFO:0008856", "metacarpal bone": "UBERON:0002374", "white matter volume measurement": "EFO:0008320", "Early-onset myopathy with fatal cardiomyopathy": "Orphanet:289377", "rat-bite fever": "EFO:1001144", "Autosomal recessive axonal neuropathy with neuromyotonia": "Orphanet:324442", "breast cancer stage": "EFO:0005607", "surface type": "EFO:0005523", "X-linked mendelian susceptibility to mycobacterial diseases": "Orphanet:319605", "neoplasm of mature T-cells or NK-cells": "EFO:0002426", "Choroid Plexus Papilloma": "EFO:1000177", "Koolen-De Vries syndrome": "Orphanet:96169", "Mesomelic dysplasia, Savarirayan type": "Orphanet:85170", "Iminoglycinuria": "Orphanet:42062", "Syndactyly type 1": "Orphanet:93402", "Charcot-Marie-Tooth disease": "Orphanet:166", "Oculocerebrofacial syndrome, Kaufman type": "Orphanet:2707", "Hypertelorism-microtia-facial clefting syndrome": "Orphanet:2213", "joint hypermobility measurement": "EFO:0007905", "facial morphology": "EFO:0004743", "basophilic myelocyte": "CL:0000614", "fat body sensu amphibia": "EFO:0000811", "cardioembolic stroke": "EFO:1001976", "growth chamber study": "EO:0007269", "rhombomere 7": "UBERON:0005523", "acute myocardial infarction": "EFO:0008583", "Scyliorhinus canicula": "NCBITaxon:7830", "Pseudomonas syringae pv. phaseolicola": "NCBITaxon:319", "breast hyperplasia": "EFO:0008492", "Pierre Robin syndrome associated with a chromosomal anomaly": "Orphanet:138047", "spindle cell tumor": "EFO:0000705", "seborrheic keratosis": "EFO:0005584", "multidrug-resistant tuberculosis": "EFO:0007381", "Sub-cortical nodular heterotopia": "Orphanet:101029", "hair cell posterior macula": "ZFA:0000281", "Lymphoproliferative syndrome": "Orphanet:238510", "X-linked lissencephaly with abnormal genitalia": "Orphanet:452", "RAD-tag": "EFO:0008879", "Familial clubfoot with or without associated lower limb anomalies": "Orphanet:199315", "intracellular part": "GO:0044424", "cortisol": "CHEBI:17650", "distal portion of anterior interventricular branch of left coronary artery": "FMA:3884", "Cardiac Tamponade": "EFO:1001285", "late congenital syphilis": "EFO:0007339", "serum albumin measurement": "EFO:0004535", "Rare genetic refraction anomaly": "Orphanet:183601", "outer ear morphology trait": "EFO:0007664", "enalapril": "CHEBI:4784", "Youcai mosaic virus": "NCBITaxon:228578", "GM17222 {http": "CLO:0014366", "3-Seq": "EFO:0008645", "norfloxacin": "CHEBI:100246", "reticulocyte count": "EFO:0007986", "Intellectual disability - alacrima - achalasia": "Orphanet:289483", "Landsberg ecotype": "EFO:0005154", "leukotriene D4": "CHEBI:28666", "Retinal arterial tortuosity": "Orphanet:75326", "cystatin C measurement": "EFO:0004617", "hypopharyngeal squamous cell carcinoma": "EFO:1001960", "Familial osteodysplasia, Anderson type": "Orphanet:2769", "squamous cell carcinoma": "EFO:0000707", "Endoplasmic Reticulum Stress": "EFO:1001886", "Periventricular nodular heterotopia": "Orphanet:98892", "Partial trisomy/tetrasomy of the short arm of chromosome 12": "Orphanet:262658", "smooth muscle tissue {http": "UBERON:0001135", "aromatic compound biosynthetic process": "GO:0019438", "sucrose": "CHEBI:17992", "Short ulna - dysmorphism - hypotonia - intellectual disability": "Orphanet:357175", "CD8-positive, CD28-negative, alpha-beta regulatory T cell": "CL:0000920", "GM17218 {http": "CLO:0013921", "FGFR3-related chondrodysplasia": "Orphanet:93420", "Folsomia candida": "NCBITaxon:158441", "Lutembacher's syndrome": "EFO:1001024", "SpDamID": "EFO:0008944", "Primary tethered chord syndrome": "Orphanet:268861", "micromolar": "UO:0000064", "anti-H3K27-3Me": "EFO:0005028", "body fat distribution": "EFO:0004341", "inosine-5'-monophosphate dehydrogenase 1 measurement": "EFO:0008158", "processed genotype data file": "EFO:0004663", "Partial deletion of chromosome 6": "Orphanet:261791", "tooth": "UBERON:0001091", "Immunoblastic Lymphadenopathy": "EFO:1001350", "Pierre Robin syndrome associated with miscellaneous anomalies": "Orphanet:138066", "astrocytoma": "EFO:0000272", "Salmonella enterica subsp. enterica serovar Gallinarum": "NCBITaxon:594", "Thumb stiffness - brachydactyly - intellectual disability": "Orphanet:1078", "Distal monosomy 20q": "Orphanet:96152", "myxedema": "EFO:1001055", "paraquat dichloride": "CHEBI:28786", "dental fluorosis": "EFO:1000892", "waist height ratio": "EFO:0005191", "phyllome {http": "PO:0006001", "CS57601": "EFO:0000029", "segmentation 1-4 somites": "EFO:0001316", "Cryptomicrotia - brachydactyly - excess fingertip arch": "Orphanet:1547", "F13": "EFO:0002711", "UV-C light regimen {http": "EO:0007129", "femtomole": "UO:0000043", "Palaemonetes pugio": "NCBITaxon:221654", "HCC1937": "EFO:0001174", "cofactor metabolic process": "GO:0051186", "maximal voluntary ventilation": "EFO:0008431", "pharyngeal arch derived gill": "UBERON:0011150", "Extrahepatic Bile Duct Adenosquamous Carcinoma": "EFO:1000247", "skin conductance level": "EFO:0006867", "Acrofacial dysostosis, Rodr\u00c3\u00adguez type": "Orphanet:1788", "post-operative fentanyl consumption measurement": "EFO:0007770", "yaws": "EFO:0007548", "basophil percentage of granulocytes": "EFO:0007995", "Eyebrow/eyelashes structural anomaly": "Orphanet:98599", "GM17207 {http": "CLO:0013881", "Neuropathy with hearing impairment": "Orphanet:139512", "Craniofrontonasal dysplasia": "Orphanet:1520", "Severe generalized recessive dystrophic epidermolysis bullosa": "Orphanet:79408", "Kit-negative, Ly-76 high orthochromatophilic erythroblasts": "CL:0002017", "Atypical Mayer-Rokitansky-K\u00c3\u00bcster-Hauser syndrome": "Orphanet:247768", "CD4-positive type I NK T cell secreting interferon-gamma": "CL:0000926", "millimole": "UO:0000040", "Autosomal recessive spastic paraplegia type 49": "Orphanet:320385", "Gallbladder Small Cell Neuroendocrine Carcinoma": "EFO:1000266", "papillary lung adenocarcinoma": "EFO:1000046", "Xylella fastidiosa": "NCBITaxon:2371", "Low Grade Fibromyxoid Sarcoma": "EFO:1000328", "duration": "EFO:0000433", "Ceratopteris thalictroides": "NCBITaxon:29596", "R1": "EFO:0002076", "High bone mass osteogenesis imperfecta": "Orphanet:314029", "fungicide": "CHEBI:24127", "coronavirus infectious disease": "EFO:0007224", "imatinib": "CHEBI:45783", "CS57848": "EFO:0000144", "fasting blood glucose measurement": "EFO:0004465", "Partial deletion of chromosome 7": "Orphanet:261796", "Low Grade Central Osteosarcoma": "EFO:1000327", "Acrodermatitis continua suppurativa of Hallopeau": "Orphanet:163931", "trefoil factor 3 measurement": "EFO:0008304", "Cloacal exstrophy": "Orphanet:93929", "dihydroxy docosatrienoic acid measurement": "EFO:0005275", "pituitary cancer": "EFO:0005578", "Charcot-Marie-Tooth disease type 1B": "Orphanet:101082", "Hypotrichosis-deafness syndrome": "Orphanet:330029", "5,6,7,8-tetrahydrobiopterin": "CHEBI:15372", "Defect in conserved oligomeric Golgi complex": "Orphanet:309568", "embryonic stage 11": "EFO:0005871", "leaf production stage": "PO:0007133", "HUES28": "EFO:0007079", "micropapillary urothelial carcinoma": "EFO:0008512", "Brain Stem Hemorrhage, Traumatic": "EFO:1001276", "SNU-620": "EFO:0006757", "Meningothelial Meningioma": "EFO:1000372", "ALG1-CDG": "Orphanet:79327", "peridontal microbiome": "EFO:0004981", "Laryngeal abductor paralysis - intellectual disability": "Orphanet:2375", "Myopathic intestinal pseudoobstruction": "Orphanet:104077", "T-cell acute lymphoblastic leukemia": "EFO:0000209", "choline alfoscerate {http": "CHEBI:16870", "heart conduction system": "UBERON:0002350", "early embryonic cell": "CL:0000007", "Constitutional dyserythropoietic anemia": "Orphanet:293830", "immune system": "UBERON:0002405", "Gallbladder Adenocarcinoma": "EFO:1000262", "Syntrichia ruralis": "NCBITaxon:38588", "BICR 22": "EFO:0006541", "mesenchymal stem cell of the bone marrow": "CL:0002540", "45,X/46,XY mixed gonadal dysgenesis": "Orphanet:1772", "dehydroepiandrosterone sulphate measurement": "EFO:0007001", "Borjeson-Forssman-Lehmann syndrome": "Orphanet:127", "Mycobacterium smegmatis": "NCBITaxon:1772", "hand dermatosis": "EFO:1000706", "Gallbladder Biliary Intraepithelial Neoplasia": "EFO:1000265", "SK-MEL-28": "EFO:0003081", "mean corpuscular hemoglobin concentration": "EFO:0004528", "narcolepsy with cataplexy": "EFO:0000614", "buttock": "UBERON:0013691", "Immune dysregulation disease with immunodeficiency": "Orphanet:169361", "chronic myeloproliferative disorder": "EFO:0002428", "Polaromonas sp. JS666": "NCBITaxon:296591", "pharyngeal squamous cell carcinoma": "EFO:1001965", "Syndromic microphthalmia": "Orphanet:202948", "Chlamydiaceae Infections": "EFO:1001288", "pergolide mesylate": "CHEBI:8021", "Methanococcus maripaludis S2": "NCBITaxon:267377", "Autosomal dominant Charcot-Marie-Tooth disease type 2M": "Orphanet:228179", "ILSXISS80/TejJ": "EFO:0002993", "Hypertryptophanemia": "Orphanet:2224", "Microphthalmia with brain and digit anomalies": "Orphanet:139471", "peanut allergic reaction": "EFO:0007425", "MOLT16": "EFO:0002239", "skin disease": "EFO:0000701", "Oligodontia": "Orphanet:99798", "female infertility": "EFO:0008560", "CS57874": "EFO:0000153", "Partial duplication of chromosome 16": "Orphanet:262672", "Rare genetic bone disease": "Orphanet:183524", "autonomic dysreflexia": "EFO:1001762", "Cobblestone lissencephaly without muscular or ocular involvement": "Orphanet:352682", "Branchiogenic deafness syndrome": "Orphanet:50815", "Pectobacterium carotovorum": "NCBITaxon:554", "Genetic intestinal disease due to fat malabsorption": "Orphanet:363306", "basophilic erythroblast": "CL:0000549", "Congenital primary megaureter, nonrefluxing and unobstructed form": "Orphanet:238654", "Chandler syndrome": "Orphanet:98979", "Familial amyloidosis, Finnish type": "Orphanet:85448", "Ochoa syndrome": "Orphanet:2704", "chronic lung allograft dysfunction": "EFO:0008497", "equine infectious anemia": "EFO:0007263", "hindbrain": "UBERON:0002028", "verrucous carcinoma": "EFO:0007535", "Amelia of upper limb, bilateral": "Orphanet:295055", "generalized anxiety disorder": "EFO:1001892", "icosenoate {http": "CHEBI:78075", "Clark level III": "EFO:0004959", "Chlorocebus aethiops": "NCBITaxon:9534", "Bullous dystrophy, macular type": "Orphanet:1867", "Borrelia burgdorferi": "NCBITaxon:139", "IVT-SAPAS": "EFO:0008783", "angiotensin converting enzyme activity measurement": "EFO:0004463", "viral exanthem": "EFO:1000776", "6-propyl-2-thiouracil": "CHEBI:8502", "Brachyolmia, Maroteaux type": "Orphanet:93302", "GM17182 {http": "CLO:0013754", "Early myoclonic encephalopathy": "Orphanet:1935", "validation by real time PCR design": "OBI:0001166", "HPAFII": "EFO:0002198", "NT-proBNP measurement": "EFO:0004745", "Exercise intolerance {http": "HP:0003546", "Respiratory insufficiency {http": "HP:0002093", "Recurrent infections - inflammatory syndrome due to zinc metabolism disorder": "Orphanet:251523", "estrogen-receptor negative breast cancer": "EFO:1000650", "Rare hypothyroidism": "Orphanet:181396", "synucleinopathy": "DOID:0050890", "17q11 microdeletion syndrome": "Orphanet:97685", "Epicanthus {http": "HP:0000286", "docosahexaenoate {http": "CHEBI:78060", "Proximal tubulopathy - diabetes mellitus - cerebellar ataxia": "Orphanet:3390", "NAMALWA": "EFO:0002246", "Adult-onset foveomacular vitelliform dystrophy": "Orphanet:99000", "collagenous colitis": "EFO:1001293", "Autosomal dominant optic atrophy plus syndrome": "Orphanet:1215", "essential tremor": "EFO:0003108", "5-oxoprolinase deficiency": "Orphanet:33572", "Spondyloepimetaphyseal dysplasia, Bieganski type": "Orphanet:168448", "ischemia": "EFO:0000556", "GM17734 {http": "CLO:0017045", "Primary immunodeficiency due to a defect in adaptive immunity": "Orphanet:179006", "Sasang constitutional medicine": "EFO:0004892", "Pfeiffer syndrome": "Orphanet:710", "Primary Peritoneal Serous Adenocarcinoma": "EFO:1000494", "fibromyalgia": "EFO:0005687", "Streptomyces reticuliscabiei": "NCBITaxon:146821", "developmental stage": "EFO:0000399", "An-1": "EFO:0006984", "Charcot-Marie-Tooth disease type 4J": "Orphanet:139515", "juvenile days 45-89": "EFO:0001302", "Acro-renal-ocular syndrome": "Orphanet:959", "Hypokalemic periodic paralysis": "Orphanet:681", "Microcephaly": "HP:0000252", "CLN4A disease": "Orphanet:228340", "Medullary sponge kidney": "Orphanet:1309", "Camptodactyly of fingers": "Orphanet:295016", "Fumaric aciduria": "Orphanet:24", "pleura": "UBERON:0000977", "Bilateral parasagittal parieto-occipital polymicrogyria": "Orphanet:208441", "Familial episodic pain syndrome with predominantly lower limb involvement": "Orphanet:391392", "4-(acetylamino)-3-hydroxyphenyl hydrogen sulfate {http": "CHEBI:82942", "Fraser syndrome": "Orphanet:2052", "GM17749 {http": "CLO:0016564", "hemoglobin measurement": "EFO:0004509", "interstitial collagenase measurement": "EFO:0008193", "ILSXISS89/TejJ": "EFO:0002996", "CS57666": "EFO:0000058", "Congenital enteropathy involving intestinal mucosa development": "Orphanet:104007", "enzyme": "OBI:0000427", "Sciatica": "HP:0011868", "Pyrobaculum aerophilum": "NCBITaxon:13773", "Holoprosencephaly - radial heart renal anomalies": "Orphanet:3186", "antipyretic": "CHEBI:35493", "PHACE syndrome": "Orphanet:42775", "response to angiotensin-converting enzyme inhibitor": "EFO:0005325", "CD7-negative lymphoid progenitor OR granulocyte monocyte progenitor": "CL:0001012", "yolk sac hematopoietic stem cell": "CL:0002354", "posterior pancreatic bud": "ZFA:0001370", "volumetric bone mineral density": "EFO:0007620", "Borderline Ovarian Mucinous Tumor": "EFO:1000138", "Ureaplasma parvum": "NCBITaxon:134821", "Autosomal recessive malignant osteopetrosis": "Orphanet:667", "Renal disease with cataract": "Orphanet:98646", "Paternal uniparental disomy of chromosome 1": "Orphanet:251004", "CD209 antigen measurement": "EFO:0008077", "Ly49D-positive natural killer cell": "CL:0002440", "Cerebral ischemia": "HP:0002637", "2-hydroxyglutarate(2-) {http": "CHEBI:11596", "occupational dermatitis": "EFO:1000744", "dorsal": "EFO:0001656", "iPS-NIHi11": "EFO:0007952", "Nephropathy-deafness-hyperparathyroidism syndrome": "Orphanet:2668", "optic disc area measurement": "EFO:0006937", "Niemann-Pick disease": "EFO:1001380", "Caenorhabditis elegans larval stage": "EFO:0007694", "X-linked Charcot-Marie-Tooth disease type 5": "Orphanet:99014", "Poly(A)-ClickSeq": "EFO:0008866", "breed": "EFO:0005238", "Progressive supranuclear palsy - parkinsonism": "Orphanet:240085", "Congenital cataract-hearing loss-severe developmental delay syndrome": "Orphanet:300313", "locus ceruleus": "UBERON:0002148", "1q21.1 microdeletion syndrome": "Orphanet:250989", "Spondylometaphyseal dysplasia, Kozlowski type": "Orphanet:93314", "SHEP-SF": "EFO:0002857", "response to vincristine": "EFO:0006950", "NCI-H2073": "EFO:0006670", "carotid artery wall cross sectional area measurement": "EFO:0007722", "scoliosis": "EFO:0004273", "transfection": "EFO:0000726", "traditional Chinese medicine type": "EFO:0007637", "zone of skin {http": "UBERON:0000014", "Appendix Adenoma": "EFO:1000089", "AG08904 {http": "CLO:0031232", "CD8-positive, alpha-beta T cell": "CL:0000625", "habitual abortion": "EFO:1000954", "pharyngeal nervous system": "EFO:0000897", "choroid-plexus macrophage": "CL:0000880", "congenital nonspherocytic hemolytic anemia": "EFO:1000641", "Disorder of gamma-aminobutyric acid metabolism": "Orphanet:79175", "imidazole": "CHEBI:50059", "3-phosphoglycerate(3-) {http": "CHEBI:57998", "Renal dysplasia - megalocystis - sirenomelia": "Orphanet:1850", "Abnormality of the abdominal organs": "HP:0002012", "Familial partial lipodystrophy associated with PLIN1 mutations": "Orphanet:280356", "host cell": "GO:0043657", "West Nile virus": "NCBITaxon:11082", "influenza infection": "EFO:0001669", "X-linked intellectual disability, Miles-Carpenter type": "Orphanet:85283", "cancer aggressiveness measurement": "EFO:0006999", "rofecoxib": "CHEBI:8887", "high density lipoprotein cholesterol measurement": "EFO:0004612", "8q22.1 microdeletion syndrome": "Orphanet:178303", "Ureter Small Cell Carcinoma": "EFO:1000610", "compatible osmolytes role": "CHEBI:23366", "CS57610": "EFO:0000032", "ergothioneine {http": "CHEBI:4828", "Duplication of the pituitary gland": "Orphanet:314621", "SUM229PE": "EFO:0006762", "Vertebrobasilar insufficiency": "EFO:1001449", "Disorder of histidine metabolism": "Orphanet:79181", "QT interval": "EFO:0004682", "motor neuron disease": "EFO:0003782", "Hypoglossia - hypodactyly": "Orphanet:989", "Epidermolysis bullosa simplex with circinate migratory erythema": "Orphanet:158681", "arm": "UBERON:0001460", "COLO 741": "EFO:0006375", "ampulla of Vater adenocarcinoma": "EFO:0008490", "Strongylocentrotus purpuratus": "NCBITaxon:7668", "maltose {http": "CHEBI:17306", "Carnitine palmitoyl transferase II deficiency, severe infantile form": "Orphanet:228305", "Left ventricular noncompaction": "Orphanet:54260", "methylation profiling": "EFO:0000751", "sebaceous adenocarcinoma": "EFO:1001171", "medulla oblongata": "UBERON:0001896", "lysosome": "GO:0005764", "hemopexin measurement": "EFO:0008149", "software variation design": "EFO:0001778", "CORL23": "EFO:0002142", "developmental dysplasia of the hip": "EFO:1000648", "mannose-binding protein C measurement": "EFO:0008224", "GM17208 {http": "CLO:0013884", "Rickettsia conorii": "NCBITaxon:781", "CS57644": "EFO:0000050", "Von Willebrand disease type 2N": "Orphanet:166093", "Autosomal dominant microcephaly": "Orphanet:2514", "Infantile dystonia-parkinsonism": "Orphanet:238455", "clinical history": "EFO:0000352", "Sigma 1278b": "EFO:0004563", "Calvarial doughnut lesions - bone fragility": "Orphanet:85192", "benign insulitis": "EFO:0002502", "Hair defect - photosensitivity - intellectual disability": "Orphanet:1408", "Postaxial polydactyly type B": "Orphanet:93335", "vibratory urticaria": "EFO:1000775", "omega-6 polyunsaturated fatty acid measurement": "EFO:0005680", "plant structure {http": "PO:0009011", "T3 B cell": "CL:0000960", "macrophage inflammatory protein 1a measurement": "EFO:0008218", "GM17826 {http": "CLO:0016518", "Central core disease": "Orphanet:597", "skeletal joint": "UBERON:0000982", "High forehead {http": "HP:0000348", "AB2": "EFO:0004043", "Diarrhea, Infantile": "EFO:1001306", "embryonic day 18": "EFO:0002569", "xanthogranulomatous pyelonephritis": "EFO:1001244", "Lung Lymphangioleiomyomatosis": "EFO:1000334", "Autosomal dominant spastic ataxia type 1": "Orphanet:251282", "distal portion of circumflex branch of left coronary artery": "FMA:3906", "Pseudoaminopterin syndrome": "Orphanet:221120", "Moderately severe hemophilia B": "Orphanet:169796", "behavioural disinhibition measurement": "EFO:0006946", "ear meristem {http": "PO:0009109", "Craniofacial-ulnar-renal syndrome": "Orphanet:293843", "Mandibuloacral dysplasia with type A lipodystrophy": "Orphanet:90153", "CCL5 measurement": "EFO:0005117", "Gossypium hirsutum": "NCBITaxon:3635", "Diarrhea-vomiting due to trehalase deficiency": "Orphanet:103909", "Clinodactyly of the 5th finger {http": "HP:0004209", "ITV": "EFO:0002065", "Autosomal recessive non-syndromic intellectual disability": "Orphanet:88616", "fusariosis": "EFO:1001795", "Porphyromonas gingivalis W83": "NCBITaxon:242619", "ovarian follicle stage I": "UBERON:2001263", "Cichorium intybus": "NCBITaxon:13427", "CD40 ligand measurement": "EFO:0004790", "non-obstructive coronary artery disease": "EFO:1001483", "GM17213 {http": "CLO:0013893", "IgG monosialylation measurement": "EFO:0008430", "Acrodysostosis with multiple hormone resistance": "Orphanet:280651", "Muscular lipidosis": "Orphanet:206953", "transmembrane glycoprotein NMB measurement": "EFO:0008303", "intestinal endoderm": "EFO:0002576", "Thin ribs - tubular bones - dysmorphism": "Orphanet:1506", "SOLiD native qual format": "EFO:0004163", "hepatitis A": "EFO:0007305", "extraembryonic cell": "CL:0000349", "Melhem-Fahl syndrome": "Orphanet:2482", "Congenital atransferrinemia": "Orphanet:1195", "inflammatory skin disease": "EFO:1000636", "embryonic stage 3": "EFO:0005862", "serotonergic drug": "CHEBI:48278", "Osteogenesis imperfecta": "Orphanet:666", "data file": "EFO:0004095", "drug-induced liver injury": "EFO:0004228", "Roussy-L\u00c3\u00a9vy syndrome": "Orphanet:3115", "cowpox": "EFO:0007225", "BMI-adjusted fasting blood insulin measurement": "EFO:0008037", "SHEF-1": "EFO:0005454", "Syndactyly type 6": "Orphanet:295012", "MMR-related febrile seizures": "EFO:0006519", "Eucalyptus globulus": "NCBITaxon:34317", "Hereditary painful callosities": "Orphanet:79141", "HELLP syndrome": "EFO:0007297", "Dental ankylosis": "Orphanet:1077", "serum amyloid A protein measurement": "EFO:0004728", "ephemeral fever": "EFO:0007258", "Vancomycin-Resistant Staphylococcus Aureus Infection": "EFO:0008558", "glycoprotein": "CHEBI:17089", "callous character": "EFO:0004891", "NCI-H1436": "EFO:0002253", "Candidatus Kuenenia stuttgartiensis": "NCBITaxon:174633", "HCC193": "EFO:0003130", "Late-onset nephronophthisis": "Orphanet:93589", "Dahl salt-sensitive": "EFO:0001350", "sepal primordium visible stage {http": "PO:0007607", "macular holes": "EFO:1001028", "femoral neck fracture": "EFO:1001792", "Spinocerebellar ataxia type 17": "Orphanet:98759", "complement C1s subcomponent measurement": "EFO:0008091", "urethra": "UBERON:0000057", "Hypotonia - cystinuria type 1": "Orphanet:238517", "percutaneous transluminal coronary angioplasty": "EFO:0003951", "Swiss19": "EFO:0006297", "Solanum phureja": "NCBITaxon:172790", "STT3B-CDG": "Orphanet:370924", "Cupriavidus metallidurans CH34": "NCBITaxon:266264", "vacuum dryer": "OBI:0400117", "Hereditary cerebral hemorrhage with amyloidosis, Icelandic type": "Orphanet:100008", "Fallopian Tube Carcinoma": "EFO:1000251", "diclofenac": "CHEBI:47381", "Cannabis use initiation": "EFO:0007586", "Intraductal Breast Papilloma": "EFO:1000306", "Ovarian Tumor of the Thecoma/Fibroma Group": "EFO:1000436", "Vibrio infectious disease": "EFO:1001235", "Salmonella enterica subsp. enterica serovar Paratyphi A": "NCBITaxon:54388", "CD8alpha-negative thymic conventional dendritic cell": "CL:0002460", "LS174T": "EFO:0002227", "Hypochromic microcytic anemia": "HP:0004840", "Iridogoniodysgenesis": "Orphanet:98634", "Vanadium": "CHEBI:27698", "exposure": "EFO:0000487", "population based design": "EFO:0001430", "opioid dependence": "EFO:0005611", "mature natural killer cell": "CL:0000824", "rosette growth stage": "PO:0007113", "Nausea": "HP:0002018", "EB1": "EFO:0002172", "Ocular Melanoma with Extraocular Extension": "EFO:1000404", "TX": "EFO:0004948", "16p13.11 microdeletion syndrome": "Orphanet:261236", "Central polydactyly of toes, unilateral": "Orphanet:295183", "milker's nodule": "EFO:0007370", "conscientiousness measurement": "EFO:0007912", "Cockayne syndrome type 2": "Orphanet:90322", "GM11993": "EFO:0001125", "Asperger syndrome": "EFO:0003757", "IgE memory B cell": "CL:0000948", "Mandibuloacral dysplasia": "Orphanet:2457", "CROAP5": "EFO:0002146", "Hs 895.T": "EFO:0006593", "Yellow fever virus": "NCBITaxon:11089", "Gastric Diffuse Large B-Cell Lymphoma": "EFO:1000270", "apical ectodermal ridge pectoral fin bud": "ZFA:0000085", "nut allergic reaction": "EFO:1001066", "cell cycle design": "EFO:0001744", "crystal cell specific anlage": "EFO:0000386", "metastatic": "EFO:0006852", "serum copper measurement": "EFO:0005267", "Ossification anomalies - psychomotor development delay": "Orphanet:73230", "acetate": "CHEBI:30089", "complement C4 measurement": "EFO:0004984", "Familial porencephaly": "Orphanet:99810", "sex": "PATO:0000047", "Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome": "Orphanet:370022", "17q11.2 microduplication syndrome": "Orphanet:139474", "GM17838 {http": "CLO:0016526", "Beta-thalassemia major": "Orphanet:231214", "azoospermia": "EFO:0000279", "Autosomal recessive cerebellar ataxia due to a DNA repair defect": "Orphanet:98097", "spinal cord interneuron": "ZFA:0000778", "Gossypium barbadense": "NCBITaxon:3634", "UBOC1": "EFO:0001259", "3-methylglutaconic aciduria": "Orphanet:289902", "Streptococcus mutans UA159": "NCBITaxon:210007", "Genetic pigmentation anomaly of the skin": "Orphanet:183463", "Sarcomatoid Carcinoma": "EFO:1000520", "glucose measurement": "EFO:0004468", "Partial deletion of the long arm of chromosome 8": "Orphanet:262065", "Diazoxide-resistant focal hyperinsulinism": "Orphanet:79298", "Constitutional mismatch repair deficiency syndrome": "Orphanet:252202", "Neurofaciodigitorenal syndrome": "Orphanet:2673", "asparaginase-induced acute pancreatitis": "EFO:1001507", "Autosomal dominant beta2-microglobulinic amyloidosis": "Orphanet:314652", "coelomic fluid": "BTO:0001708", "Glycogen storage disease due to acid maltase deficiency, infantile onset": "Orphanet:308552", "LC2/AD": "EFO:0003140", "systemic juvenile idiopathic arthritis": "EFO:1001999", "molar mass unit": "UO:0000055", "Combined immunodeficiency due to STK4 deficiency": "Orphanet:314689", "Larynx anomaly": "Orphanet:156249", "iPS-11a": "EFO:0007099", "Albers-Sch\u00c3\u00b6nberg osteopetrosis": "Orphanet:53", "mucinous cystadenocarcinoma": "EFO:0007378", "International Unit": "EFO:0002927", "7-methylxanthine {http": "CHEBI:48991", "mesothelioma": "EFO:0000588", "visceral Leishmaniasis": "EFO:0005045", "HCC1534": "EFO:0006428", "epithelium of pancreatic duct": "UBERON:0009970", "schistosomiasis": "EFO:1001475", "anti-Mullerian hormone measurement": "EFO:0004769", "Esophageal malformation": "Orphanet:88993", "Genetic intractable diarrhea of infancy": "Orphanet:363300", "Tetraamelia - multiple malformations": "Orphanet:3301", "Familial ovarian cancer": "Orphanet:213517", "Brain dopamine-serotonin vesicular transport disease": "Orphanet:352649", "response to antihypertensive drug": "EFO:0005405", "aging": "GO:0007568", "Virus": "NCBITaxon:10239", "primary high content screen": "EFO:0007556", "X-linked Charcot-Marie-Tooth disease type 4": "Orphanet:101078", "spinal muscular atrophy": "EFO:0008525", "Glycerol kinase deficiency, adult form": "Orphanet:284414", "UACC812": "EFO:0001258", "microliter": "UO:0000101", "incomplete abortion": "EFO:1001799", "Ta stage": "EFO:0005309", "CS57543": "EFO:0000009", "tumor size": "EFO:0004134", "Ly49H-positive natural killer cell": "CL:0002444", "KYSE-270": "EFO:0006629", "(2-hydroxyphenyl)acetate {http": "CHEBI:62423", "Pelizaeus-Merzbacher disease in female carriers": "Orphanet:280229", "Spondylometaphyseal dysplasia - bowed forearms - facial dysmorphism": "Orphanet:168552", "panuveitis": "EFO:1001082", "22Rv1": "EFO:0002095", "Cardiofaciocutaneous syndrome": "Orphanet:1340", "exemestane": "CHEBI:4953", "Chudley-McCullough syndrome": "Orphanet:314597", "Malpighian tubule main body primordium": "FBbt:00005501", "Blepharophimosis-intellectual disability syndrome due to UBE3B deficiency": "Orphanet:329255", "filarial elephantiasis": "EFO:0007272", "Hypocalcemia": "HP:0002901", "chlorpyrifos": "CHEBI:34631", "rough endoplasmic reticulum": "GO:0005791", "Methanobrevibacter smithii ATCC 35061": "NCBITaxon:420247", "Glaucoma secondary to spherophakia/ectopia lentis and megalocornea": "Orphanet:238763", "Bardet-Biedl syndrome 4": "EFO:0009024", "cerebrospinal fluid volume measurement": "EFO:0008080", "oral candidiasis": "EFO:0007406", "ovarian adenoma benign": "EFO:0002507", "organophosphate biosynthetic process": "GO:0090407", "Thanatophoric dysplasia": "Orphanet:2655", "Non-acquired combined pituitary hormone deficiency": "Orphanet:467", "primordial midbrain channel": "UBERON:2005017", "Small for gestational age {http": "HP:0001518", "visna": "EFO:0007542", "vasculature of eye": "UBERON:0002203", "CCFSTTG1": "EFO:0002127", "HUVEC cell line": "EFO:0002795", "Chondrodysplasia punctata": "Orphanet:93442", "Monosomy X": "Orphanet:99226", "calpain I measurement": "EFO:0008064", "Partial autosomal monosomy": "Orphanet:98142", "retinoic acid receptor responder protein 2 measurement": "EFO:0008274", "Beta-thalassemia": "Orphanet:848", "Gyps": "NCBITaxon:8965", "childhood acute myeloid leukemia": "EFO:0000330", "Genetic syndrome with limb malformations as a major feature": "Orphanet:404577", "Abnormality of the bladder": "HP:0000014", "Spindle Cell Melanoma": "EFO:1000546", "Triticum dicoccon {http": "NCBITaxon:49225", "apparent mineralocorticoid excess syndrome": "EFO:1000817", "response to antimetabolite": "GO:0097329", "O-acetylcarnitine {http": "CHEBI:73024", "scanned image": "EFO:0004094", "interleukin 17 receptor D measurement": "EFO:0008177", "Primary systemic amyloidosis": "Orphanet:314701", "obese body mass index status": "EFO:0007041", "embryonic anal pad": "FBbt:00005748", "bone marrow cell": "CL:0002092", "Bonnemann-Meinecke-Reich syndrome": "Orphanet:1261", "LMNA-related cardiocutaneous progeria syndrome": "Orphanet:363618", "Frank-Ter Haar syndrome": "Orphanet:137834", "CLOVE syndrome": "Orphanet:140944", "Alternaria alternata": "NCBITaxon:5599", "family history of breast cancer": "EFO:0005606", "Isolated sulfite oxidase deficiency": "Orphanet:99731", "protein": "CHEBI:36080", "amnioserosa": "UBERON:0010302", "Brachydactyly type B2": "Orphanet:140908", "Autosomal dominant spastic paraplegia type 4": "Orphanet:100985", "Micropapillary Serous Carcinoma": "EFO:1000377", "Glycogen storage disease due to muscle and heart glycogen synthase deficiency": "Orphanet:137625", "phenyl hydrogen sulfate {http": "CHEBI:27905", "Oryza sativa cv. Nipponbare": "EFO:0007587", "3MC syndrome 2": "EFO:1001977", "random exon sequencing": "EFO:0003746", "Autosomal agammaglobulinemia": "Orphanet:33110", "IRIDA syndrome": "Orphanet:209981", "Populus yunnanensis": "NCBITaxon:242124", "ampicillin": "CHEBI:28971", "CB185": "EFO:0004048", "nasopharyngeal neoplasm": "EFO:0004252", "Familial idiopathic steroid-resistant nephrotic syndrome": "Orphanet:656", "tetraploid": "PATO:0001382", "ChIP-seq": "EFO:0002692", "Non-distal trisomy 10q": "Orphanet:1695", "cervical carcinoma": "EFO:0001061", "BrdU-CLIP": "EFO:0008658", "Rubus idaeus": "NCBITaxon:32247", "peste des petits ruminants infectious disease": "EFO:0007431", "Autosomal recessive multiple pterygium syndrome": "Orphanet:2990", "ENBREL": "EFO:0002669", "spontaneous pneumothorax": "HP:0002108", "Autosomal dominant optic atrophy and late-onset deafness": "Orphanet:255117", "Pseudomonas mendocina": "NCBITaxon:300", "Anorectal malformation": "Orphanet:96346", "Isolated optic nerve hypoplasia": "Orphanet:137902", "Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency": "Orphanet:289307", "NHDL cholesterol": "EFO:0005688", "Distal Xq28 microduplication syndrome": "Orphanet:293939", "mastitis": "EFO:1001034", "response to thioamide": "EFO:0007633", "Tufted angioma": "Orphanet:1063", "polychlorinated biphenyls measurement": "EFO:0007042", "sporophyte senescent stage": "PO:0007017", "pneumococcal bacteremia": "EFO:1001925", "OAW42": "EFO:0006705", "Fatal multiple mitochondrial dysfunction syndrome type 1": "Orphanet:401869", "Citrus clementina": "NCBITaxon:85681", "serum IgG glycosylation measurement": "EFO:0005193", "Rare genetic gastroenterological disease": "Orphanet:165652", "Autosomal dominant distal hereditary motor neuropathy": "Orphanet:140465", "Jackson-Weiss syndrome": "Orphanet:1540", "Colorectal Diffuse Large B-Cell Lymphoma": "EFO:1000191", "endothelial cell of coronary artery": "CL:2000018", "CapSeq": "EFO:0008673", "Lung Sclerosing Hemangioma": "EFO:1000337", "Illumina sequencing": "OBI:0000724", "Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures": "Orphanet:73229", "milligram per kilogram body weight": "EFO:0005354", "Beta-thalassemia intermedia": "Orphanet:231222", "Familial primary hypomagnesemia with normocalciuria and normocalcemia": "Orphanet:34527", "immunoprecipitation assay": "OBI:0001700", "Borrelia infectious disease": "EFO:1000842", "bromocriptine methanesulfonate": "CHEBI:3182", "response to hydrochlorothiazide": "EFO:0005202", "rhombomere 1": "UBERON:0005499", "(2,4-dichlorophenoxy)acetic acid": "CHEBI:28854", "Dominant beta-thalassemia": "Orphanet:231226", "Ischemic stroke": "HP:0002140", "carotid artery stiffness measurement": "EFO:0007718", "NCI-H358": "EFO:0002291", "Sleep Disorder": "EFO:0008568", "Polymicrogyria due to TUBB2B mutation": "Orphanet:300573", "Bacillus thuringiensis": "NCBITaxon:1428", "SCC-9": "EFO:0006485", "chromoblastomycosis": "EFO:0007207", "Adult-onset autosomal dominant leukodystrophy": "Orphanet:99027", "Kandori fleck retina": "Orphanet:99179", "Subcutaneous Panniculitis-Like T-Cell Lymphoma": "EFO:1000552", "Benign Ovarian Mucinous Tumor": "EFO:1000115", "Moderate multiminicore disease with hand involvement": "Orphanet:178145", "Break-seq": "EFO:0008659", "Epstein Barr virus nuclear antigen 1 IgG measurement": "EFO:0007790", "PEAT": "EFO:0008859", "Est": "EFO:0006986", "cytoplasmic part": "GO:0044444", "feather": "UBERON:0000022", "thiopurines": "CHEBI:35666", "stromal cell": "CL:0000499", "gallbladder carcinoma": "EFO:1001956", "3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol": "CHEBI:63919", "X-linked adrenoleukodystrophy": "Orphanet:43", "3MC syndrome 1": "EFO:1001978", "Liver Inflammatory Myofibroblastic Tumor": "EFO:1000324", "animal phobia": "EFO:1001876", "PA-TU-8988S": "EFO:0006730", "biological macromolecule": "EFO:0004446", "Fried's tooth and nail syndrome": "Orphanet:99672", "iritis": "EFO:1000997", "Dentinogenesis imperfecta type 2": "Orphanet:166260", "validation by reverse transcription PCR design": "OBI:0001162", "Silene latifolia": "NCBITaxon:37657", "induces sterile inflammation": "EFO:0004367", "ND02579 {http": "CLO:0014404", "GM14440 {http": "CLO:0031257", "O-oleoylcarnitine {http": "CHEBI:72689", "Amelo-cerebro-hypohidrotic syndrome": "Orphanet:1946", "Lung Sarcomatoid Carcinoma": "EFO:1000336", "Benign Salivary Gland Myoepithelioma": "EFO:1000119", "cellular aromatic compound metabolic process": "GO:0006725", "hindgut anlage": "FBbt:00004202", "Ocular Sebaceous Carcinoma": "EFO:1000405", "Panax ginseng": "NCBITaxon:4054", "Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia": "Orphanet:79091", "Patterned dystrophy of the retinal pigment epithelium": "Orphanet:63454", "Bone dysplasia, lethal Holmgren type": "Orphanet:1842", "heat tolerance": "TO:0000259", "corpuscles of Stannius": "UBERON:2001200", "Methyl-seq": "EFO:0008804", "Duplication of urethra": "Orphanet:237", "Gamma-glutamylcysteine synthetase deficiency": "Orphanet:33574", "Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency": "Orphanet:308425", "high content screen of cells treated with library of siRNAs": "EFO:0007551", "Stromal Predominant Kidney Wilms Tumor": "EFO:1000551", "basal cell adhesion molecule measurement": "EFO:0008032", "Syndromic hair shaft abnormality": "Orphanet:79367", "GM06990": "EFO:0002783", "Distal myopathy with vocal cord weakness": "Orphanet:600", "FaDu": "EFO:0002178", "embryonal carcinoma": "EFO:0004986", "GM17191 {http": "CLO:0013793", "toll-like receptor 4": "EFO:0008301", "Disorder of cobalamin metabolism and transport": "Orphanet:79171", "Genetic central nervous system malformation": "Orphanet:183506", "tarsal tunnel syndrome": "EFO:1001208", "aspartate aminotransferase, cytoplasmic measurement": "EFO:0008031", "Biliary atresia": "Orphanet:30391", "IgA plasma cell": "CL:0000987", "geniculate herpes zoster": "EFO:0007281", "Onthophagus nigriventris": "NCBITaxon:476074", "Episodic flaccid weakness {http": "HP:0003752", "connective tissue": "CL:0000388", "Alopecia": "Orphanet:79364", "juvenile vascular leaf": "PO:0006339", "Thiemann disease, familial form": "Orphanet:3314", "thiamine metabolic process": "GO:0006772", "podoconiosis": "EFO:0004712", "T-helper 17 cell": "CL:0000899", "CD38-negative unswitched memory B cell": "CL:0002111", "Mucopolysaccharidosis type 4A": "Orphanet:309297", "musculature": "UBERON:0001015", "Apis mellifera mellifera": "NCBITaxon:44477", "CD94-positive natural killer cell": "CL:0002441", "somite 1": "UBERON:2000072", "pancreatic carcinoma": "EFO:0002618", "mutant strain": "EFO:0004006", "NCI-H1650": "EFO:0002260", "SLC35A2-CDG": "Orphanet:356961", "CHGA cleavage product measurement": "EFO:0007909", "rectal bleeding": "HP:0002573", "megakaryocyte-erythroid progenitor cell": "CL:0000050", "Nm-seq": "EFO:0008828", "HEK-293H": "EFO:0001183", "L-glutamine": "CHEBI:18050", "hyomandibula": "ZFA:0000672", "Cervical Large Cell Neuroendocrine Carcinoma": "EFO:1000167", "Proximal spinal muscular atrophy type 2": "Orphanet:83418", "platelet-to-lymphocyte ratio": "EFO:0008446", "coenzyme Q10 measurement": "EFO:0007836", "Coregonus clupeaformis": "NCBITaxon:59861", "hindgut anlage in statu nascendi": "FBbt:00005424", "Deinococcus radiodurans": "NCBITaxon:1299", "Syringocystadenoma Papilliferum": "EFO:1000558", "PancTUI": "EFO:0002715", "Calcifying Nested Epithelial Stromal Tumor of the Liver": "EFO:1000149", "D dimer measurement": "EFO:0004507", "Action myoclonus - renal failure syndrome": "Orphanet:163696", "JEG3": "EFO:0002066", "Aloe vera": "NCBITaxon:34199", "Male infertility with azoospermia or oligozoospermia due to single gene mutation": "Orphanet:399805", "Erythrocyte galactose epimerase deficiency": "Orphanet:308473", "Autosomal recessive centronuclear myopathy": "Orphanet:169186", "Familial dysautonomia": "Orphanet:1764", "Meningioma": "Orphanet:2495", "abdominal wall": "UBERON:0003697", "16p13.3 microduplication syndrome": "Orphanet:96078", "Medullar aplasia": "Orphanet:182040", "pole plasm": "FBbt:00004891", "Adult-onset distal myopathy due to VCP mutation": "Orphanet:329478", "adult foregut precursor": "FBbt:00005611", "nucleoside metabolic process": "GO:0009116", "Myeloperoxidase deficiency": "Orphanet:2587", "glypican-5 measurement": "EFO:0008139", "ILSXISS90/TejJ": "EFO:0002997", "Osteogenesis imperfecta type 4": "Orphanet:216820", "atrioventricular node disease": "EFO:0005305", "hemoglobin A2 measurement": "EFO:0005845", "dermoid cyst": "EFO:1000894", "facial width measurement": "EFO:0007855", "Perturb-Seq": "EFO:0008860", "Partial monosomy of the short arm of chromosome 20": "Orphanet:261992", "ureter": "UBERON:0000056", "unit of flow rate": "EFO:0004418", "tacrine": "CHEBI:45980", "Illumina Genome Analyzer II standard manufacturer's protocol": "EFO:0005083", "vertebral column structure": "EFO:0001369", "Rare disease with autism": "Orphanet:180772", "Rare genetic adrenal disease": "Orphanet:183637", "diffuse cutaneous Leishmaniasis": "EFO:1001784", "Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form": "Orphanet:308698", "Congenital absence of both lower leg and foot, unilateral": "Orphanet:295097", "Partial deletion of chromosome 19": "Orphanet:261841", "T-Cell Prolymphocytic Leukemia": "EFO:1000560", "B4GALT1-CDG": "Orphanet:79332", "Multiple endocrine neoplasia type 1": "Orphanet:652", "CS57664": "EFO:0000057", "biceps femoris": "UBERON:0001374", "amount": "PATO:0000070", "glucose homeostasis": "GO:0042593", "Ophrys fusca": "NCBITaxon:145942", "Short stature - deafness - neutrophil dysfunction - dysmorphism": "Orphanet:2866", "Ulnar-mammary syndrome": "Orphanet:3138", "Chromosome conformation capture assay": "EFO:0007688", "Cholangitis": "HP:0030151", "lens of camera-type eye": "UBERON:0000965", "progression free survival": "EFO:0004920", "Pantherophis obsoletus": "NCBITaxon:39099", "Torsade-de-pointes syndrome with short coupling interval": "Orphanet:51084", "Brachytelephalangy - dysmorphism - Kallmann syndrome": "Orphanet:1295", "irritable bowel syndrome": "EFO:0000555", "post dauer stage": "EFO:0005511", "cleft lip": "EFO:0003959", "Atrial stand still": "Orphanet:1344", "Ogataea angusta": "NCBITaxon:870730", "serum hepcidin measurement": "EFO:0004504", "Lithognathus mormyrus": "NCBITaxon:50591", "(-)-cotinine {http": "CHEBI:68641", "Partial duplication of the long arm of chromosome 3": "Orphanet:262851", "GM14502 {http": "CLO:0031510", "Microphthalmia - cataract": "Orphanet:2543", "promethazine": "CHEBI:8461", "46,XY disorder of sex development due to cholesterol synthesis defect": "Orphanet:325511", "necrotizing ulcerative gingivitis": "EFO:1001058", "paragraph delayed recall measurement": "EFO:0006806", "fibronectin measurement": "EFO:0008133", "ESHyb": "EFO:0003972", "segmentation 5-9 somites": "EFO:0001317", "SHP77": "EFO:0002328", "Penile Carcinoma": "EFO:1000465", "Hypogonadotropic hypogonadism - retinitis pigmentosa": "Orphanet:2235", "Thermoplasma acidophilum DSM 1728": "NCBITaxon:273075", "plexiform neurofibroma": "EFO:0000658", "biological role": "CHEBI:24432", "Lodderomyces elongisporus NRRL YB-4239": "NCBITaxon:379508", "Metaphyseal dysplasia - maxillary hypoplasia - brachydacty": "Orphanet:2504", "Senecio aethnensis": "NCBITaxon:121540", "Theiler stage 9": "EFO:0004401", "vanoxerine dihydrochloride": "CHEBI:64086", "CS57824": "EFO:0000132", "cadherin-5 measurement": "EFO:0008060", "polygonal cell": "CL:0000398", "Epithelioid Cell Uveal Melanoma": "EFO:1000244", "Monosomy Xp21": "Orphanet:261476", "rhombomere 5": "UBERON:0005515", "Ovarian Embryonal Carcinoma": "EFO:1000415", "cholesteatoma of middle ear": "EFO:1000678", "differentiated": "EFO:0002954", "Congenital insensitivity to pain with hyperhidrosis": "Orphanet:217399", "lobe attachment": "EFO:0007667", "Ehlers-Danlos/osteogenesis imperfecta syndrome": "Orphanet:230857", "46,XX disorder of sex development induced by fetal androgens excess": "Orphanet:90776", "TRPV4-related bone disorder": "Orphanet:364820", "Fraction E immature B cell": "CL:0002054", "Partial deletion of chromosome 8": "Orphanet:261801", "trunk": "UBERON:0002100", "X-linked intellectual disability with isolated growth hormone deficiency": "Orphanet:67045", "Cockayne syndrome type 1": "Orphanet:90321", "Fc receptor-like protein 3 measurement": "EFO:0008127", "X-linked intellectual disability, Cilliers type": "Orphanet:163971", "JL-1": "EFO:0006448", "slow muscle cell somite 10": "ZFA:0001047", "Autosomal recessive hyper-IgE syndrome": "Orphanet:169446", "venous thromboembolism": "EFO:0004286", "Partial deletion of chromosome 11": "Orphanet:261816", "human gut metagenome": "NCBITaxon:408170", "intelligence": "EFO:0004337", "Familial isolated hypoparathyroidism due to agenesis of parathyroid gland": "Orphanet:2239", "nighttime rest measurement": "EFO:0007827", "Isolated growth hormone deficiency type III": "Orphanet:231692", "insulin metabolic clearance rate measurement": "EFO:0006830", "Thyroid Gland Undifferentiated (Anaplastic) Carcinoma": "EFO:1000595", "Col-5": "EFO:0005153", "Macular coloboma - cleft palate - hallux valgus": "Orphanet:91494", "Fundus albipunctatus": "Orphanet:227796", "theobromine {http": "CHEBI:28946", "Autosomal recessive spastic paraplegia type 62": "Orphanet:401785", "exendin-4": "CHEBI:64073", "Blepharophimosis-intellectual disability syndrome, Verloes type": "Orphanet:293725", "inclusion body myositis": "EFO:0007323", "COG5-CDG": "Orphanet:263487", "2-acetylaminofluorene": "CHEBI:17356", "(R)-2-hydroxy-4-methylpentanoate {http": "CHEBI:55535", "Inclusion myopathy": "Orphanet:206662", "pectoral limb scapula": "UBERON:0001124", "acatalasia": "EFO:0004144", "posterior caudal vein": "UBERON:2001063", "memory T cell": "CL:0000813", "Graham Little-Piccardi-Lassueur syndrome": "Orphanet:505", "Ehlers-Danlos syndrome, classic type": "Orphanet:287", "adiponectin measurement": "EFO:0004502", "atrial fibrillation": "EFO:0000275", "Unilateral renal hypoplasia": "Orphanet:97361", "microliter per liter": "EFO:0004413", "glutarate(2-) {http": "CHEBI:30921", "OVTOKO": "EFO:0006728", "Wolff-Parkinson-White Syndrome": "EFO:1001450", "G401.6": "EFO:0005703", "TARP syndrome": "Orphanet:2886", "NCI-H1693": "EFO:0006661", "alpha-methyl-L-dopa": "CHEBI:61058", "skeletal tuberculosis": "EFO:0007487", "mammary epithelial cell": "CL:0002327", "acute pancreatitis": "EFO:1000652", "DOK": "EFO:0006564", "(10Z)-heptadecenoate {http": "CHEBI:78990", "single-organism cellular process": "GO:0044763", "Brachyolmia type 1, Toledo type": "Orphanet:93303", "mathematical ability": "EFO:0004875", "Trisomy 5p": "Orphanet:1742", "Adult Krabbe disease": "Orphanet:206448", "GM17759 {http": "CLO:0016607", "Dent disease type 2": "Orphanet:93623", "Microcornea - corectopia - macular hypoplasia": "Orphanet:2535", "Townes-Brocks syndrome": "Orphanet:857", "enterobiasis": "EFO:0007254", "BE(2)-C": "EFO:0005725", "motor development measurement": "EFO:0008237", "bladder disease": "EFO:1000018", "Patent ductus arteriosus {http": "HP:0001643", "Disorder of biogenic amine metabolism and transport": "Orphanet:79214", "Strand-seq": "EFO:0008952", "corpus cardiacum": "UBERON:0001056", "chemotherapy-induced gastrointestinal mucositis": "EFO:1001880", "Intellectual disability-hyperkinetic movement-truncal ataxia syndrome": "Orphanet:369847", "Bacillus anthracis": "NCBITaxon:1392", "gnathal primordium": "FBbt:00005534", "Sarcosinemia": "Orphanet:3129", "Thanatophoric dysplasia type 1": "Orphanet:1860", "adrenocortical adenoma": "EFO:0003104", "panic disorder without agoraphobia": "EFO:1001907", "Nuphar advena": "NCBITaxon:77108", "Glycogen storage disease due to muscle glycogen phosphorylase deficiency": "Orphanet:368", "spinal fracture": "EFO:0003902", "Genetic non-syndromic central nervous system malformation": "Orphanet:269550", "response to cetuximab": "EFO:0007682", "minor salivary gland": "UBERON:0001830", "Hereditary hyperekplexia": "Orphanet:3197", "Streptomyces bikiniensis": "NCBITaxon:1896", "Microcystic Meningioma": "EFO:1000376", "posterior lateral line nerve": "UBERON:2000175", "resting heart rate": "EFO:0004351", "Chronic intestinal pseudoobstruction": "Orphanet:2978", "Lactuca sativa": "NCBITaxon:4236", "effector memory CD8-positive, alpha-beta T cell": "CL:0000913", "cognitive impairment measurement": "EFO:0007998", "dynein light chain roadblock-type 1 measurement": "EFO:0008114", "ammonium sulfate": "CHEBI:62946", "GM17787 {http": "CLO:0016685", "SW403": "EFO:0002366", "Encephalopathy due to hydroxykynureninuria": "Orphanet:79155", "aspartate aminotransferase measurement": "EFO:0004736", "rostral blood island": "UBERON:2005029", "gamma-delta thymocyte": "CL:0002405", "SELEX": "EFO:0008917", "Niemann-Pick disease type C": "Orphanet:646", "bodily fluid": "UBERON:0006314", "beta-alanine {http": "CHEBI:16958", "extra-ocular muscle": "UBERON:0001601", "exercise": "EFO:0000483", "glycerophosphoethanolamine {http": "CHEBI:36314", "Polymicrogyria - turricephaly - hypogenitalism": "Orphanet:2925", "prootic": "UBERON:0004746", "Thymic Sarcomatoid Carcinoma": "EFO:1000577", "Familial Mediterranean fever": "Orphanet:342", "X-linked cerebral adrenoleukodystrophy": "Orphanet:139396", "host cell cytoplasm": "GO:0030430", "endoplasmic reticulum aminopeptidase 1 measurement": "EFO:0008119", "Keratosis follicularis spinulosa decalvans": "Orphanet:2340", "Mesomelia-synostoses syndrome": "Orphanet:2496", "Autosomal dominant multiple pterygium syndrome": "Orphanet:65743", "Cenani-Lenz syndrome": "Orphanet:3258", "Leukoencephalopathy with bilateral anterior temporal lobe cysts": "Orphanet:139444", "microarray wash station": "EFO:0002028", "CS57870": "EFO:0000150", "GM17276 {http": "CLO:0013199", "Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism": "Orphanet:399846", "Ralstonia pickettii": "NCBITaxon:329", "Menorrhagia": "HP:0000132", "Leprechaunism": "Orphanet:508", "Theiler stage 14": "EFO:0004405", "Medicago truncatula": "NCBITaxon:3880", "Hyperphalangy": "Orphanet:295002", "Eschscholzia californica": "NCBITaxon:3467", "Microcephalic osteodysplastic primordial dwarfism type II": "Orphanet:2637", "ventral tegmental area": "UBERON:0002691", "hemorrhagic disease of newborn": "EFO:1000964", "X-linked central congenital hypothyroidism with late-onset testicular enlargement": "Orphanet:329235", "Cardiovirus infectious disease": "EFO:0007194", "Finnish upper limb-onset distal myopathy": "Orphanet:399086", "molar": "UO:0000062", "Paxillus filamentosus": "NCBITaxon:85986", "trans/trans-18": "EFO:0006826", "brain ventricle": "UBERON:0004086", "alpha-linolenic acid {http": "CHEBI:27432", "Rare genetic hepatic disease": "Orphanet:156601", "malignant pleural mesothelioma": "EFO:0000770", "organophosphate metabolic process": "GO:0019637", "sclerosing cholangitis": "EFO:0004268", "Spinocerebellar ataxia type 7": "Orphanet:94147", "neuroticism measurement": "EFO:0007660", "Classic congenital lipoid adrenal hyperplasia due to STAR deficency": "Orphanet:325524", "Auriculoosteodysplasia": "Orphanet:114", "IgA short lived plasma cell": "CL:0000976", "HUES3": "EFO:0007080", "glycodeoxycholate {http": "CHEBI:82982", "Mus musculus x Mus spretus": "NCBITaxon:186842", "Microcephaly - brachydactyly - kyphoscoliosis": "Orphanet:3433", "progenitor cell of endocrine pancreas": "CL:0002351", "Genetic thrombotic microangiopathy": "Orphanet:183589", "Systemic disease with cataract": "Orphanet:98643", "floor plate neural rod": "UBERON:2000887", "Colorectal Squamous Cell Carcinoma": "EFO:1000198", "Abnormality of the thyroid gland": "HP:0000820", "bullous skin disease": "EFO:1000673", "SCARF syndrome": "Orphanet:3134", "POEMS syndrome": "EFO:1001115", "urethritis": "EFO:0003878", "CS57840": "EFO:0000140", "C-C motif chemokine 8 measurement": "EFO:0008055", "distal renal artery": "EFO:0002593", "large cell lung carcinoma": "EFO:0003050", "Mucopolysaccharidosis type 4B": "Orphanet:309310", "Hereditary acrokeratotic poikiloderma of Kindler-Weary": "Orphanet:306539", "olfactory lobe": "UBERON:0005366", "GM09583 {http": "CLO:0011394", "Paternal uniparental disomy of chromosome 14": "Orphanet:96334", "discrete subaortic stenosis": "EFO:1000901", "Postaxial acrofacial dysostosis": "Orphanet:246", "Influenza A virus": "NCBITaxon:11320", "Saccharina latissima": "NCBITaxon:309358", "Dubin-Johnson syndrome": "Orphanet:234", "X-linked intellectual disability - seizures - psoriasis": "Orphanet:3052", "Neisseria meningitidis": "NCBITaxon:487", "7-methylguanine {http": "CHEBI:2274", "Cerebral arteriovenous malformation": "Orphanet:46724", "Zygodactyly type 4": "Orphanet:295193", "energy expenditure measurement": "EFO:0008005", "upper digestive tract": "UBERON:0004908", "CD56-positive, CD161-positive immature natural killer cell": "CL:0002338", "Marfanoid syndrome, De Silva type": "Orphanet:2464", "establishment of localization": "GO:0051234", "LS 180": "EFO:0006640", "Ritter's disease": "EFO:0007473", "middle lobe syndrome": "EFO:0007367", "Mesomelic dysplasia, Kantaputra type": "Orphanet:1836", "Secretory apparatus of the lacrimal system anomaly": "Orphanet:98603", "cingulate cortex": "UBERON:0003027", "DF5033": "EFO:0004068", "small intestine primordium": "FBbt:00005504", "Qualitative or quantitative defects of nebulin": "Orphanet:209182", "response to placebo": "EFO:0008344", "cholesteatoma of attic": "EFO:1000676", "Partial deletion of chromosome 16": "Orphanet:261826", "GM17801 {http": "CLO:0016492", "response to corticosteroid": "GO:0031960", "Lactobacillus crispatus": "NCBITaxon:47770", "Pseudohypoaldosteronism type 2B": "Orphanet:88939", "Lacrimal Gland Adenoid Cystic Carcinoma": "EFO:1000317", "myrcene": "CHEBI:17221", "GM15242 {http": "CLO:0027447", "esophageal squamous cell carcinoma": "EFO:0005922", "growth condition design": "EFO:0001759", "3\u00e2\u0080\u0099NT method": "EFO:0008642", "SUM52PE": "EFO:0001246", "TC71": "EFO:0002865", "Prader-Willi-like syndrome": "Orphanet:398073", "tassel inflorescence {http": "PO:0020126", "candesartan": "CHEBI:3347", "Diazoxide-sensitive diffuse hyperinsulinism": "Orphanet:165985", "NCI-H1838": "EFO:0002268", "response to carbamazepine": "EFO:0008484", "Pituitary Gland Adenoma": "EFO:1000478", "Generalized dominant dystrophic epidermolysis bullosa": "Orphanet:231568", "Trigonocephaly - broad thumbs": "Orphanet:3365", "paraquat": "CHEBI:34905", "neutrophil percentage of leukocytes": "EFO:0007990", "EEM syndrome": "Orphanet:1897", "myocardium of ventricle {http": "UBERON:0001083", "PAPERCLIP": "EFO:0008844", "pulmonary hypertension": "EFO:0001361", "Unilateral hemispheric polymicrogyria": "Orphanet:101071", "Chlamydophila infectious disease": "EFO:1000863", "hyphal cell": "CL:0000286", "GM12762": "EFO:0001153", "Thrombocytopenia - absent radius": "Orphanet:3320", "FTH1-related iron overload": "Orphanet:247790", "bronchial neoplasm": "EFO:1000849", "Familial pancreatic carcinoma": "Orphanet:1333", "sacrum": "UBERON:0003690", "Marchantia polymorpha subsp. polymorpha {http": "NCBITaxon:1480153", "CS57825": "EFO:0000133", "Rare dyslipidemia": "Orphanet:101953", "Eucalyptus grandis": "NCBITaxon:71139", "placebo": "EFO:0001674", "Ring chromosome 10": "Orphanet:1438", "recurrent pneumonia": "EFO:0007461", "placental pericyte": "EFO:0005024", "EMG": "HP:0003458", "Trisomy 10p": "Orphanet:171929", "Dravet syndrome": "Orphanet:33069", "somite 12": "UBERON:2000851", "Ngari virus": "NCBITaxon:273357", "pooled clone sequencing": "EFO:0003741", "Juvenile Polymyositis": "EFO:1001988", "Nakajo-Nishimura syndrome": "Orphanet:2615", "RPMI8226": "EFO:0002322", "interaction with host via secreted substance involved in symbiotic interaction": "GO:0052048", "ATC Code B Blood and blood forming organs": "EFO:0005635", "Focal facial dermal dysplasia type IV": "Orphanet:398189", "U2OS": "EFO:0002869", "Haemophilus influenzae meningitis": "EFO:1000955", "Autosomal dominant cerebellar ataxia type 2": "Orphanet:208508", "immature CD1a-positive Langerhans cell": "CL:0001016", "Distal monosomy 10q": "Orphanet:96148", "Metabolic disease with pigmentary retinitis": "Orphanet:98713", "Hereditary hypotrichosis with recurrent skin vesicles": "Orphanet:217407", "Salmonella bongori": "NCBITaxon:54736", "Hyperbiliverdinemia": "Orphanet:276405", "HIV infection": "EFO:0000764", "Fusarium cerealis": "NCBITaxon:56641", "Charcot-Marie-Tooth disease type 4B2": "Orphanet:99956", "Supranuclear oculomotor palsy": "Orphanet:98687", "Lymphedema - cleft palate": "Orphanet:86917", "Congenital intrinsic factor deficiency": "Orphanet:332", "Central congenital hypothyroidism": "Orphanet:226298", "Arterial tortuosity syndrome": "Orphanet:3342", "ligament": "UBERON:0000211", "iPSC derived cell line": "EFO:0005740", "GM12869": "EFO:0005342", "response to lamotrigine": "EFO:0007661", "methylation profiling by array": "EFO:0002759", "Blomstrand lethal chondrodysplasia": "Orphanet:50945", "Calu3": "EFO:0002819", "tumor grading": "OBI:0600002", "Congenital sucrase-isomaltase deficiency with starch and lactose intolerance": "Orphanet:306474", "Mesoaxial synostotic syndactyly with phalangeal reduction": "Orphanet:157801", "CytoSeq": "EFO:0008703", "agrochemical role": "CHEBI:33286", "extracellular membrane-bounded organelle": "GO:0065010", "cervical adenocarcinoma cell line": "EFO:0005217", "FISSEQ": "EFO:0008990", "Signet Ring Cell Gastric Adenocarcinoma": "EFO:1000524", "tobramycin": "CHEBI:28864", "gender identity disorder": "EFO:0008587", "Epilepsy telangiectasia": "Orphanet:1951", "histoplasmosis": "EFO:0007310", "benomyl": "CHEBI:3015", "NCI-H1993": "EFO:0002272", "Dengue virus 1": "NCBITaxon:11053", "gamma-linolenic acid measurement": "EFO:0007762", "ideomotor apraxia": "EFO:1000980", "presumptive dorsal mesoderm": "ZFA:0000265", "megakaryocyte": "CL:0000556", "non-substance related disinhibited behaviour": "EFO:0005432", "(R)-lactic acid": "CHEBI:42111", "3T3-F442A": "EFO:0002811", "interferon beta": "EFO:0003023", "radiation quality treatment": "EO:0007154", "cryptococcal meningitis": "EFO:0007228", "Disorder of peptide metabolism": "Orphanet:79187", "ILSXISS41/TejJ": "EFO:0002983", "Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis": "Orphanet:65288", "thyroid gland sarcoma": "EFO:1001971", "Crane-Heise syndrome": "Orphanet:1512", "gram": "UO:0000021", "gamma-delta intraepithelial T cell": "CL:0000801", "asbestos": "CHEBI:46661", "Tumor Lysis Syndrome": "EFO:1001479", "embryonic brain": "UBERON:6001060", "Deafness - hypogonadism": "Orphanet:90646", "GM11832": "EFO:0001120", "Hereditary neutrophilia": "Orphanet:279943", "mucosal type mast cell": "CL:0000485", "Mosaic trisomy 20": "Orphanet:1724", "serum IgE measurement": "EFO:0004579", "sunburn": "EFO:0003958", "biexponential transformation": "OBI:0200006", "mbd5 associated neurodevelopmental disorder": "EFO:0009072", "cytochrome P450": "CHEBI:38559", "spine bone mineral density change measurement": "EFO:0008474", "Nasal obstruction": "HP:0001742", "Early-onset non-syndromic cataract": "Orphanet:217052", "Autosomal dominant Charcot-Marie-Tooth disease type 2O": "Orphanet:284232", "Pythium ultimum": "NCBITaxon:65071", "palmitoleic acid measurement": "EFO:0007973", "geotrichosis": "EFO:0007284", "Mucolipidosis type 4": "Orphanet:578", "Spinocerebellar ataxia type 5": "Orphanet:98766", "Erythroderma desquamativum": "Orphanet:314", "46,XX disorder of gonadal development": "Orphanet:325055", "Tetra-amelia": "Orphanet:294971", "Genetic renal tumor": "Orphanet:183595", "Complex hereditary spastic paraplegia": "Orphanet:102013", "Acanthopleura": "NCBITaxon:61362", "Severe neonatal-onset encephalopathy with microcephaly": "Orphanet:209370", "myoglobin": "CHEBI:7044", "Cupriavidus metallidurans": "NCBITaxon:119219", "derived MAGE-TAB array data matrix file": "EFO:0004099", "rhombomere 4": "UBERON:0005511", "Tibial hemimelia, unilateral": "Orphanet:295077", "Pseudohypoparathyroidism type 1C": "Orphanet:79444", "MERRF": "Orphanet:551", "fetal liver hematopoietic progenitor cell": "CL:0002353", "Polydactyly of a biphalangeal thumb, unilateral": "Orphanet:295144", "inDrop": "EFO:0008780", "Peeling skin syndrome type A": "Orphanet:263548", "Neurometabolic disorder due to serine deficiency": "Orphanet:35705", "oligohydramnios": "EFO:0007401", "staphylococcal skin infections": "EFO:1001849", "Spastic paraplegia - precocious puberty": "Orphanet:2826", "tetraethylenepentamine": "CHEBI:49798", "QRS amplitude": "EFO:0007742", "Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity": "Orphanet:53583", "Macular dystrophy {http": "HP:0007754", "Ivemark syndrome": "Orphanet:97548", "CS57641": "EFO:0000049", "Mevalonic aciduria": "Orphanet:29", "Streptomyces aureofaciens": "NCBITaxon:1894", "Behcet's syndrome": "EFO:0003780", "Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1": "Orphanet:137681", "COLO829": "EFO:0002140", "pyruvate decarboxylase deficiency": "EFO:0007459", "gene expression protocol": "EFO:0003788", "Salvelinus fontinalis": "NCBITaxon:8038", "Arthrogryposis - renal dysfunction - cholestasis": "Orphanet:2697", "Brassica oleracea var. alboglabra": "NCBITaxon:3714", "Distal myopathy with posterior leg and anterior hand involvement": "Orphanet:63273", "Sandhoff disease, adult form": "Orphanet:309169", "nocardiosis": "EFO:0007397", "abdominal aortic fatty streak": "EFO:0005600", "magnesium ion homeostasis": "GO:0010960", "lymph node tingible body macrophage": "CL:0000888", "Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome": "Orphanet:306542", "anatomical modifier": "EFO:0001646", "Milroy disease": "Orphanet:79452", "Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect": "Orphanet:280671", "Glycogen storage disease due to liver phosphorylase kinase deficiency": "Orphanet:264580", "partial sensory epilepsy": "EFO:1001090", "cornea": "UBERON:0000964", "cytokine measurement": "EFO:0004873", "aspartic acid {http": "CHEBI:22660", "Abnormality of carboxylic acid metabolism": "HP:0004354", "atypical teratoid rhabdoid tumor": "EFO:1002008", "Phytophthora sojae": "NCBITaxon:67593", "WM793-P1N1": "EFO:0002874", "life expectancy": "EFO:0004299", "Isolated diffuse palmoplantar keratoderma": "Orphanet:307148", "iPS-18c": "EFO:0007107", "Partial duplication of the long arm of chromosome 13": "Orphanet:262932", "Gastric Adenoma": "EFO:1000268", "retroperitoneal cancer": "EFO:0007466", "DU4475": "EFO:0002168", "Cystic fibrosis - gastritis - megaloblastic anemia": "Orphanet:2575", "tonsillectomy risk measurement": "EFO:0007924", "Gallbladder Adenosquamous Carcinoma": "EFO:1000264", "acetylsalicylic acid": "CHEBI:15365", "SE.00 stem elongation begins stage {http": "PO:0007079", "Microcystic Renal Disease": "EFO:0008621", "Bladder Squamous Cell Carcinoma": "EFO:1000130", "small intestine neuroendocrine tumor": "EFO:1001928", "Charcot-Marie-Tooth disease type 2R": "Orphanet:397968", "Aspergillus oryzae RIB40": "NCBITaxon:510516", "wheat allergic reaction": "EFO:1001243", "olfactory neurosphere cell line": "EFO:0005705", "Anophthalmia - megalocornea - cardiopathy - skeletal anomalies": "Orphanet:1101", "mesenchymal stem cell": "EFO:0000586", "theca cell layer": "UBERON:0000155", "cognition": "EFO:0003925", "Eyebrow/eyelashes hypertrichosis": "Orphanet:98595", "protein kinase C inhibitor": "CHEBI:37700", "Genetic neurodegenerative disease with dementia": "Orphanet:276058", "esophagus muscularis mucosa": "UBERON:0004648", "prothoracic leg disc": "FBbt:00001781", "19p13.12 microdeletion syndrome": "Orphanet:254346", "Melopsittacus undulatus": "NCBITaxon:13146", "Colon Inflammatory Polyp": "EFO:1000184", "UKE1": "EFO:0006307", "hyperplasia": "EFO:0000536", "smooth muscle of esophagus": "UBERON:0002112", "abscess": "EFO:0003030", "T-B- severe combined immunodeficiency": "Orphanet:317419", "Trypanosoma cruzi seropositivity": "EFO:0005530", "Multiple benign circumferential skin creases on limbs": "Orphanet:2505", "NIH3T3": "EFO:0001222", "MCF 10A": "EFO:0001200", "ML-DmBG1-c1": "EFO:0005821", "Juvenile hyaline fibromatosis": "Orphanet:2028", "phenotype": "EFO:0000651", "Tricho-retino-dento-digital syndrome": "Orphanet:1264", "Autosomal recessive spastic paraplegia type 44": "Orphanet:320401", "neutrophil percentage of granulocytes": "EFO:0007994", "Kluyveromyces lactis": "NCBITaxon:28985", "CS57875": "EFO:0000154", "inflorescence development stage {http": "PO:0001083", "mitochondrial DNA measurement": "EFO:0006312", "Dysplasia of head of femur, Meyer type": "Orphanet:168621", "interstitial cystitis": "EFO:0008507", "Cervical Intraepithelial Neoplasia Grade 2/3": "EFO:1000166", "interleukin (Rattus norvegicus)": "EFO:0003793", "Skin Basosquamous Cell Carcinoma": "EFO:1000529", "NCI-H650": "EFO:0002298", "uncultured sulfate-reducing bacterium": "NCBITaxon:153939", "Theiler stage 1": "EFO:0004393", "bleomycin A2": "CHEBI:3139", "microsporidiosis": "EFO:0007366", "Autosomal dominant limb-girdle muscular dystrophy type 1C": "Orphanet:265", "Bardet-Biedl syndrome 7": "EFO:0009026", "ototoxicity": "EFO:0006951", "Lung Giant Cell Carcinoma": "EFO:1000332", "epigenetic status": "EFO:0000473", "Ectodermal dysplasia syndrome": "Orphanet:79373", "study design": "EFO:0001426", "enucleate erythrocyte": "CL:0000595", "monoblast": "CL:0000040", "sap": "EFO:0001047", "Parietal encephalocele": "Orphanet:268826", "hemochromatosis": "EFO:1000642", "decidual natural killer cell": "CL:0002343", "maculopapular eruption": "EFO:1001253", "auxin": "EFO:0005900", "microgametophyte {http": "PO:0025280", "mbn2": "EFO:0005820", "subcorneal pustular dermatosis": "EFO:1000771", "MESSA": "EFO:0002233", "White forelock with malformations": "Orphanet:2475", "Placental Hemangioma": "EFO:1000480", "High Grade Surface Osteosarcoma": "EFO:1000296", "Rare hereditary disease with peripheral neuropathy": "Orphanet:207015", "macrophage scavenger receptor types I and II measurement": "EFO:0008222", "Look-Seq": "EFO:0008787", "Congenital dyserythropoietic anemia type II": "Orphanet:98873", "sleep apnea": "EFO:0003877", "Apodia": "Orphanet:294986", "Autosomal recessive spastic paraplegia type 68": "Orphanet:401825", "epithalamus": "UBERON:0001899", "Brachydactyly-syndactyly, Zhao type": "Orphanet:93409", "Syndromic orbital border hypoplasia": "Orphanet:98606", "Dickkopf-related protein 3 measurement": "EFO:0008109", "Familial  hyperprolactinemia": "Orphanet:397685", "macrophage metalloelastase measurement": "EFO:0008220", "periodontitis": "EFO:0000649", "interleukin 1 beta measurement": "EFO:0008166", "GM17126 {http": "CLO:0015124", "Distal myotilinopathy": "Orphanet:98911", "Microcephalic primordial dwarfism": "Orphanet:324761", "17beta-estradiol": "CHEBI:16469", "Caenorhabditis remanei": "NCBITaxon:31234", "Paroxysmal dyskinesia": "Orphanet:1431", "right": "EFO:0001659", "17q21.31 microduplication  syndrome": "Orphanet:217340", "lateral ventricle volume measurement": "EFO:0008487", "RTS3b": "EFO:0006748", "Spondyloepimetaphyseal dysplasia with multiple dislocations": "Orphanet:93360", "GM17264 {http": "CLO:0013168", "diverticulitis": "EFO:1001460", "Carpenter-Waziri syndrome": "Orphanet:93973", "myeloid neoplasm": "EFO:0002427", "cultivar": "EFO:0005136", "Abnormality of gastrointestinal vasculature": "HP:0004296", "FlowSeq": "EFO:0008744", "hypodermyiasis": "EFO:0007320", "abnormality of the abdomen morphology": "HP:0001438", "Gingival fibromatosis - facial dysmorphism": "Orphanet:2025", "hypermetropia": "HP:0000540", "acquired aplastic anemia": "EFO:0006926", "intracranial hypotension": "EFO:1000993", "Achondrogenesis": "Orphanet:932", "nervous system cancer": "EFO:0007392", "Plasmodium falciparum antigen IgG measurement": "EFO:0007812", "Malignant Pancreatic Neoplasm": "EFO:1000359", "Clark level I": "EFO:0004957", "acute coronary syndrome": "EFO:0005672", "reciprocal translocation": "EFO:0004022", "nuocyte": "CL:0002089", "Microcephalic primordial dwarfism, Dauber type": "Orphanet:319675", "Obesity due to leptin receptor gene deficiency": "Orphanet:179494", "ornithine {http": "CHEBI:18257", "pectoral fin skeleton": "UBERON:0010710", "mefloquine": "CHEBI:63609", "Pleural Epithelioid Mesothelioma": "EFO:1000484", "Shoulder and girdle defects - familial intellectual disability": "Orphanet:2580", "AIDS": "EFO:0000765", "CD11c-low plasmacytoid dendritic cell": "CL:0000989", "Not NOTCH3-related small vessel disease of the brain": "Orphanet:77304", "Spinocerebellar ataxia type 19/22": "Orphanet:98772", "response to perphenazine": "GO:0097334", "Short stature - pituitary and cerebellar defects - small sella turcica": "Orphanet:85442", "labral sensory complex primordium": "FBbt:00005546", "Genetic cerebellar malformation": "Orphanet:269560", "dourine": "EFO:0007240", "Recessive hereditary methemoglobinemia type 2": "Orphanet:139380", "GM14503 {http": "CLO:0031509", "Ectopia lentis - chorioretinal dystrophy - myopia": "Orphanet:1884", "immature alpha-beta T cell": "CL:0000790", "Generalized pustular psoriasis": "Orphanet:247353", "Plasmodium falciparum malaria": "EFO:0007444", "A3/KAW": "EFO:0006532", "Congenital disorder of glycosylation with epilepsy as a major feature": "Orphanet:371071", "pre-conventional dendritic cell": "CL:0002010", "Callipepla californica": "NCBITaxon:67771", "paranasal sinus neoplasm": "EFO:0003866", "FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome": "Orphanet:404451", "sweat gland": "UBERON:0001820", "Severe X-linked intellectual disability, Gustavson type": "Orphanet:3078", "Menkes disease": "Orphanet:565", "Holzgreve-Wagner-Rehder syndrome": "Orphanet:2167", "Adrenogenital syndrome": "Orphanet:181412", "colonic epithelium cell line": "BTO:0003250", "Mitochondrial disease with eye involvement": "Orphanet:98695", "Immunodeficiency due to CD25 deficiency": "Orphanet:169100", "Hermansky-Pudlak syndrome type 8": "Orphanet:231537", "Paternal 20q13.2q13.3 microdeletion syndrome": "Orphanet:261304", "cytochalasin B": "CHEBI:23527", "thigh": "UBERON:0000376", "CS57803": "EFO:0000122", "technical replicate": "EFO:0002090", "Sorghum bicolor": "NCBITaxon:4558", "endometrial endometrioid carcinoma": "EFO:1001514", "Maternally-inherited progressive external ophthalmoplegia": "Orphanet:663", "Dichelobacter nodosus": "NCBITaxon:870", "macrophage inflammatory protein 1b measurement": "EFO:0008219", "769P": "EFO:0002099", "random chromosome sequencing": "EFO:0003745", "Gasterosteus aculeatus": "NCBITaxon:69293", "organism part comparison design": "EFO:0001750", "polychlorinated biphenyls": "CHEBI:35446", "cell specimen": "OBI:0001468", "8q21.11 microdeletion syndrome": "Orphanet:284160", "Congenital patella dislocation, bilateral": "Orphanet:295237", "response to clozapine": "GO:0097338", "dibenzothiazepine": "CHEBI:39268", "Abnormal eye movements": "Orphanet:98691", "Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome": "Orphanet:404476", "Elevated serum creatine phosphokinase {http": "HP:0003236", "Capra hircus": "NCBITaxon:9925", "X-linked spastic paraplegia type 34": "Orphanet:171607", "Lactobacillus parabuchneri": "NCBITaxon:152331", "azathioprine": "CHEBI:2948", "family relationship": "EFO:0004424", "Neonatal death {http": "HP:0003811", "Opisthokonta {http": "NCBITaxon:33154", "Charcot-Marie-Tooth disease type 1C": "Orphanet:101083", "cerebral amyloid angiopathy": "EFO:0006790", "haploid deletion library": "EFO:0007561", "pharyngeal pouch 5": "UBERON:0007126", "Motor delay {http": "HP:0001270", "X-linked intellectual disability - corpus callosum agenesis - spastic quadriparesis": "Orphanet:85330", "sexual dimorphism": "EFO:0005951", "Cerebellar-facial-dental syndrome": "EFO:0009030", "Severe combined immunodeficiency due to CORO1A deficiency": "Orphanet:228003", "Hemoglobinopathy Toms River": "Orphanet:280615", "NCI-H1930": "EFO:0002270", "fibroblast growth factor 2 measurement": "EFO:0008129", "biosequence provider": "EFO:0001730", "PTB-Seq": "EFO:0008874", "Von Willebrand disease type 2M": "Orphanet:166090", "COLO 783": "EFO:0006376", "Split hand-split foot malformation": "Orphanet:2440", "Macropus eugenii": "NCBITaxon:9315", "Proteus syndrome": "Orphanet:744", "autosomal recessive disease": "EFO:1000017", "Theiler stage 17": "EFO:0002583", "Phosphoribosylpyrophosphate synthetase superactivity": "Orphanet:3222", "Kabuki syndrome": "Orphanet:2322", "Acute neonatal citrullinemia type I": "Orphanet:247546", "Glycogen storage disease due to glycogen branching enzyme deficiency": "Orphanet:367", "Streptomyces avermitilis": "NCBITaxon:33903", "pregnanediol-3-glucuronide {http": "CHEBI:88765", "HCC1569": "EFO:0001173", "endoglin measurement": "EFO:0008118", "Spinocerebellar ataxia type 18": "Orphanet:98771", "Genetic recurrent myoglobinuria": "Orphanet:99845", "Floor of Mouth Mucoepidermoid Carcinoma": "EFO:1000260", "Digestive System Mixed Adenoneuroendocrine Carcinoma": "EFO:1000219", "Siegler-Brewer-Carey syndrome": "Orphanet:3167", "Cucumber mosaic virus": "NCBITaxon:12305", "NCI-H23": "EFO:0002286", "inclusion conjunctivitis": "EFO:0007324", "Non-distal monosomy 7p": "Orphanet:96136", "anthropometric measurement": "EFO:0004302", "Aroclor 1254": "CHEBI:63933", "RERF-LC-OK": "EFO:0006744", "Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11": "Orphanet:231147", "GFP protein fusion library": "EFO:0007566", "eyelid": "UBERON:0001711", "Palpebral piliary tumor": "Orphanet:98590", "Illumina native qseq format": "EFO:0004164", "NCI-H125": "EFO:0003116", "warfarin": "CHEBI:10033", "Familial atypical multiple mole melanoma syndrome": "Orphanet:404560", "Familial hypofibrinogenemia": "Orphanet:101041", "Isolated focal palmoplantar keratoderma": "Orphanet:307846", "phosphate-containing compound metabolic process": "GO:0006796", "Osteochondrosis of genetic origin": "Orphanet:399391", "Pancreatic beta cell agenesis with neonatal diabetes mellitus": "Orphanet:28455", "kidney disease": "EFO:0003086", "SNU-668": "EFO:0006759", "response to zileuton": "EFO:0007676", "bundle sheath {http": "PO:0006023", "MAP kinase-activated protein kinase 2 measurement": "EFO:0008225", "liver enzyme measurement": "EFO:0004582", "mosquito bite measurement": "EFO:0008376", "gallbladder": "UBERON:0002110", "CS57785": "EFO:0000118", "bleomycin": "CHEBI:22907", "SN56.B5.G4": "EFO:0002081", "dedifferentiated chondrosarcoma": "EFO:0000394", "Facioscapulohumeral dystrophy": "Orphanet:269", "pelvic fin bud": "ZFA:0001384", "Rare genetic coagulation disorder": "Orphanet:183654", "Idiopathic juvenile osteoporosis": "Orphanet:85193", "Congenital anonychia": "Orphanet:79143", "high throughput sequencer": "EFO:0002699", "Leishmania mexicana": "NCBITaxon:5665", "Sialuria": "Orphanet:3166", "GM15056 {http": "CLO:0030328", "Oculopharyngodistal myopathy": "Orphanet:98897", "Saccharomyces bayanus MCYC 623": "NCBITaxon:226127", "KYSE-70": "EFO:0006633", "Hemoglobin Lepore - beta-thalassemia": "Orphanet:330032", "2q23.1 microdeletion syndrome": "Orphanet:228402", "Hyperlipoproteinemia type 1": "Orphanet:411", "X-linked ichthyosis syndrome": "Orphanet:281210", "Hypothyroidism due to deficient transcription factors involved in pituitary development or function": "Orphanet:226307", "epithelial cell of prostate": "CL:0002231", "nemonapride": "CHEBI:31899", "lipodystrophy": "EFO:1000727", "Mosaic trisomy 1": "Orphanet:1692", "Drosophile simulans MD106": "EFO:0004032", "steroid lipomatosis": "EFO:1000769", "organic substance metabolic process": "GO:0071704", "bud {http": "PO:0000055", "Pyropia yezoensis": "NCBITaxon:2788", "ISS": "EFO:0008989", "Dreissena polymorpha": "NCBITaxon:45954", "cibarium primordium": "FBbt:00017019", "Tachyglossus aculeatus": "NCBITaxon:9261", "Kleefstra syndrome": "Orphanet:261494", "RL": "EFO:0002319", "Acropectorovertebral dysplasia": "Orphanet:957", "17beta-hydroxy-5alpha-androstan-3-one": "CHEBI:16330", "response to thiazide": "EFO:0007981", "Spinocerebellar ataxia type 34": "Orphanet:1955", "Megacystis-microcolon-intestinal hypoperistalsis syndrome": "Orphanet:2241", "O(4')-sulfo-L-tyrosine {http": "CHEBI:46215", "developmental process": "GO:0032502", "SL": "EFO:0007031", "laryngeal squamous cell carcinoma": "EFO:0006352", "Farber lipogranulomatosis": "Orphanet:333", "persulfide dioxygenase ETHE1, mitochondrial measurement": "EFO:0008258", "response to allogeneic hematopoietic stem cell transplant": "EFO:0007044", "Xenopus laevis x Xenopus muelleri": "NCBITaxon:481606", "schwannoma": "EFO:0000693", "cranial ganglion": "UBERON:0001714", "Alpha-thalassemia - myelodysplastic syndrome": "Orphanet:231401", "Daphnia pulex": "NCBITaxon:6669", "thrombomodulin measurement": "EFO:0007774", "Sordaria macrospora": "NCBITaxon:5147", "Receptive language delay {http": "HP:0010863", "peritonsillar abscess": "EFO:0007429", "gallbladder disease": "EFO:0003832", "DN2a thymocyte": "CL:0002423", "GM14468 {http": "CLO:0031281", "Salmonella enterica subsp. enterica serovar Abortusovis": "NCBITaxon:53961", "BC-2": "EFO:0002045", "Cleft palate - large ears - small head": "Orphanet:2013", "salicyluric acid {http": "CHEBI:9008", "Subcortical band heterotopia": "Orphanet:99796", "cartilage thickness measurement": "EFO:0007873", "transcription profiling by RT-PCR": "EFO:0002943", "Transient bullous dermolysis of the newborn": "Orphanet:79411", "oligoclonal band measurement": "EFO:0005206", "salmeterol": "CHEBI:9011", "Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency": "Orphanet:289527", "Aceruloplasminemia": "Orphanet:48818", "Oculocutaneous albinism type 1A": "Orphanet:79431", "interleukin 10 measurement": "EFO:0004750", "Hallermann-Streiff syndrome": "Orphanet:2108", "GRIP": "EFO:0008755", "4470": "EFO:0002807", "Laurin-Sandrow syndrome": "Orphanet:2378", "Polyvalvular heart disease syndrome": "Orphanet:228410", "double negative thymocyte": "CL:0002489", "leukoplakia of tongue": "EFO:0006885", "Fusobacterium nucleatum": "NCBITaxon:851", "SF295": "EFO:0005452", "zinc sulfate": "CHEBI:35176", "trichloroethylene": "CHEBI:16602", "homocysteine": "CHEBI:17230", "N,N-dimethylglycine {http": "CHEBI:17724", "Methylobacterium extorquens AM1": "NCBITaxon:272630", "delivery measurement": "EFO:0006922", "dye swap replicate": "EFO:0002092", "Borderline Ovarian Clear Cell Tumor": "EFO:1000136", "bladder carcinoma": "EFO:0000292", "GM12717": "EFO:0001148", "Festuca brevipila": "NCBITaxon:98746", "Rare constitutional hemolytic anemia due to an enzyme disorder": "Orphanet:98369", "burning mouth syndrome": "EFO:1000850", "GM17767 {http": "CLO:0016593", "Kit-positive granulocyte monocyte progenitor": "CL:0002002", "Congenital bile acid synthesis defect type 2": "Orphanet:79303", "3-hydroxyisovalerate {http": "CHEBI:82957", "OVISE": "EFO:0006724", "neuronal stem cell": "CL:0000047", "ribonucleoside biosynthetic process": "GO:0042455", "Genetic gastro-esophageal disease": "Orphanet:165658", "TERV-ST110": "EFO:0001252", "carotid artery disease": "EFO:0003781", "renal system": "UBERON:0001008", "EKVX": "EFO:0006786", "polycythemia": "EFO:0005804", "DN3 thymocyte": "CL:0000807", "Genetic hypertension": "Orphanet:156629", "Burkitts lymphoma": "EFO:0000309", "classifier prediction": "EFO:0000347", "T4a tumor stage": "EFO:0004945", "methyl alpha-D-glucopyranoside {http": "CHEBI:320061", "Fusarium sp.": "NCBITaxon:29916", "lysosomal protective protein measurement": "EFO:0008215", "Autosomal dominant neovascular inflammatory vitreoretinopathy": "Orphanet:329211", "Autosomal dominant spastic paraplegia type 36": "Orphanet:320365", "rhabdomyolysis": "EFO:0003867", "184B5 cell": "BTO:0002180", "Distal trisomy 14q": "Orphanet:1705", "motexafin gadolinium": "CHEBI:50161", "Agammaglobulinemia - microcephaly - craniosynostosis - severe dermatitis": "Orphanet:83617", "Kit-positive, CD34-positive common myeloid progenitor": "CL:0001023", "response to ribavirin": "GO:1901559", "Lissencephaly type 3 - familial fetal akinesia sequence": "Orphanet:86821", "copine-1 measurement": "EFO:0008102", "oxygen": "CHEBI:15379", "pharynx cancer": "EFO:0005577", "Distal monosomy 14q": "Orphanet:96150", "Cannabis sativa": "NCBITaxon:3483", "Pierre Robin syndrome associated with bone disease": "Orphanet:138055", "altitude sickness": "EFO:1000782", "Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature": "Orphanet:308041", "interleukin-21 (Mus musculus)": "EFO:0003804", "Genetic hypoparathyroidism": "Orphanet:208593", "agoraphobia symptom measurement": "EFO:0007945", "TK22": "EFO:0004091", "Intestinal Type Adenocarcinoma": "EFO:1000304", "Brachydactyly - nystagmus - cerebellar ataxia": "Orphanet:1246", "biomarker": "CHEBI:59163", "Mosaic trisomy 9": "Orphanet:99776", "Petrolisthes cinctipes": "NCBITaxon:88211", "Ichthyosis-cheek-eyebrow syndrome": "Orphanet:2267", "hair": "UBERON:0001037", "basal cell": "CL:0000646", "cGMP-specific 3',5'-cyclic phosphodiesterase measurement": "EFO:0008081", "Leber plus disease": "Orphanet:99718", "nasal cavity": "UBERON:0001707", "Aggregatibacter actinomycetemcomitans": "NCBITaxon:714", "Falco rusticolus": "NCBITaxon:120794", "CEDNIK syndrome": "Orphanet:66631", "Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis": "Orphanet:93218", "Neosartorya fischeri": "NCBITaxon:36630", "facial hair thickness measurement": "EFO:0007823", "GM17221 {http": "CLO:0014377", "Mixed Lobular and Ductal Breast Carcinoma": "EFO:1000382", "septic abortion": "EFO:1001177", "NSM": "EFO:0005495", "3-hydroxy-1-methylpropylmercapturic acid measurement": "EFO:0007015", "vitamin A measurement": "EFO:0004857", "sperm motility measurement": "EFO:0008578", "Tibio-fibular synostosis": "Orphanet:295028", "Congenital sodium diarrhea": "Orphanet:103908", "bromochloroacetic acid": "CHEBI:64206", "MPDU1-CDG": "Orphanet:79323", "IgG plasma cell": "CL:0000985", "The International HapMap Project": "EFO:0002911", "Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome": "Orphanet:391348", "184A1N4 cell": "BTO:0002179", "Hereditary cryohydrocytosis with reduced stomatin": "Orphanet:168577", "Spinocerebellar ataxia type 12": "Orphanet:98762", "tinea pedis": "EFO:0007512", "antenna": "UBERON:0000972", "Progressive myoclonic epilepsy with dystonia": "Orphanet:352596", "RERF-LC-KJ": "EFO:0002851", "Genetic central nervous system and retinal vascular disease": "Orphanet:183503", "G140": "EFO:0006403", "nodular nonsuppurative panniculitis": "EFO:1000742", "Genetic lens and zonula anomaly": "Orphanet:183607", "quetiapine": "CHEBI:8707", "Genetic interstitial lung disease": "Orphanet:264992", "Alopecia - intellectual disability - hypergonadotropic hypogonadism": "Orphanet:1014", "cerebellum": "UBERON:0002037", "GM17279 {http": "CLO:0013210", "Tibial aplasia - ectrodactyly": "Orphanet:3329", "sporadic Creutzfeld Jacob disease": "EFO:1000656", "Aegilops tauschii": "NCBITaxon:37682", "Congenital stromal corneal dystrophy": "Orphanet:101068", "SW780": "EFO:0002371", "entorhinal cortical volume": "EFO:0005092", "osmotic diuretic": "CHEBI:50504", "Acro-renal-mandibular syndrome": "Orphanet:958", "sodium valproate": "CHEBI:9925", "calcium ionophore": "CHEBI:22986", "iron(III) dicitrate": "CHEBI:4991", "FAST-SeqS": "EFO:0008738", "benzodiazepine": "CHEBI:22720", "10-nonadecenoate {http": "CHEBI:83052", "translation profiling": "EFO:0001033", "GM14405 {http": "CLO:0031201", "Gastric Metaplasia": "EFO:1000273", "peripheral nervous system": "UBERON:0000010", "dehydroepiandrosterone": "CHEBI:28689", "CS57541": "EFO:0000008", "Orofaciodigital syndrome type 13": "Orphanet:141330", "Desulfotomaculum reducens MI-1": "NCBITaxon:349161", "Julidochromis marlieri": "NCBITaxon:32499", "Partial deletion of the long arm of chromosome 12": "Orphanet:261821", "heart rate": "EFO:0004326", "application": "CHEBI:33232", "Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome": "Orphanet:293967", "Lyme disease": "EFO:0008510", "Autosomal recessive limb-girdle muscular dystrophy type 2H": "Orphanet:1878", "Abnormality of the pinna": "HP:0000377", "chemical role": "CHEBI:51086", "Fusarium {http": "NCBITaxon:5506", "CD8_alpha-low Langerhans cell": "CL:0001015", "ChIP-exo": "EFO:0005302", "Apis mellifera ligustica": "NCBITaxon:7469", "Zellweger syndrome": "Orphanet:912", "Lower limb hypertrophy": "Orphanet:295051", "hypocotyl {http": "PO:0020100", "Conjunctival Nevus": "EFO:1000205", "CD27-low, CD11b-high natural killer cell": "CL:0002348", "Chronic Hepatitis C infection": "EFO:0004220", "hypopharyngeal sense organ": "EFO:0003397", "Autosomal dominant spondylocostal dysostosis": "Orphanet:1797", "embryonic maxillary sensory complex": "FBbt:00005618", "calcium chloride": "CHEBI:3312", "cochlear hair cell": "CL:0000202", "ductus arteriosus": "UBERON:0005440", "spina bifida": "EFO:0003105", "Autosomal dominant spastic paraplegia type 10": "Orphanet:100991", "Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome": "EFO:0009028", "eosinophilic esophagitis": "EFO:0004232", "GM17204 {http": "CLO:0013835", "secondary biliary cirrhosis": "EFO:1001487", "Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria": "Orphanet:293284", "Yersinia pestis": "NCBITaxon:632", "Neurodegenerative syndrome due to cerebral folate transport deficiency": "Orphanet:217382", "saccharin {http": "CHEBI:32111", "B-1a B cell": "CL:0000820", "hepatic schizont": "EFO:0002589", "skeleton": "UBERON:0004288", "aortic valve insufficiency": "EFO:0007148", "aleurone layer": "PO:0005360", "X-linked intellectual disability, Zorick type": "Orphanet:85337", "breast carcinoma": "EFO:0000305", "HCT116": "EFO:0002824", "Partial deletion of chromosome 9": "Orphanet:261806", "Limb-mammary syndrome": "Orphanet:69085", "Benign familial neonatal seizures": "Orphanet:1949", "mPAC L20": "EFO:0006656", "Nematoda infectious disease": "EFO:0007391", "thymic plasmacytoid dendritic cell": "CL:0000942", "GDM1": "EFO:0002183", "Disorder of ketone body metabolism": "Orphanet:79183", "paraneoplastic pemphigus": "EFO:0008602", "pectoral girdle": "ZFA:0000407", "Schnitzler syndrome": "EFO:1001165", "Aprosencephaly cerebellar dysgenesis": "Orphanet:1126", "CMLT1": "EFO:0002134", "Lotus uliginosus": "NCBITaxon:181288", "response to red blood cell transfusion": "EFO:0006802", "regulation of gene expression": "GO:0010468", "Onycho-patellar syndrome with eye involvement": "Orphanet:98704", "Dubowitz syndrome": "Orphanet:235", "duodenal ulcer": "EFO:0004607", "hardware manufacturer": "EFO:0001737", "Rectal Tubular Adenoma": "EFO:1000504", "Autosomal recessive spastic paraplegia type 56": "Orphanet:320411", "O-glutarylcarnitine {http": "CHEBI:73040", "Familial generalized lentiginosis": "Orphanet:231040", "response to 5' fluorouracil": "GO:0036275", "melanoma": "EFO:0000756", "sphingomyelin d18": "CHEBI:106363", "presumptive segmental plate": "UBERON:0007282", "retinal vein occlusion": "EFO:1001157", "white matter lesion progression measurement": "EFO:0007746", "lobe size": "EFO:0007666", "L-arginine": "CHEBI:16467", "Dysostosis of genetic origin": "Orphanet:404568", "Laryngeal Small Cell Carcinoma": "EFO:1000320", "clomipramine hydrochloride": "CHEBI:3755", "Female infertility due to fertilization defect": "Orphanet:404469", "hemometra": "EFO:1000962", "Influenza A seropositivity": "EFO:0007038", "uterine carcinoma": "EFO:0002919", "CD69-positive, CD4-positive single-positive thymocyte": "CL:0002433", "Endometritis": "EFO:1001312", "Familial exudative vitreoretinopathy": "Orphanet:891", "Southern bean mosaic virus": "NCBITaxon:12139", "basophil": "CL:0000767", "Lysosomal disease with restrictive cardiomyopathy": "Orphanet:217638", "Down syndrome": "EFO:0001064", "gene name": "EFO:0002605", "Congenital muscular dystrophy with integrin alpha-7 deficiency": "Orphanet:34520", "immature CD16-positive myeloid dendritic cell": "CL:0002533", "Hemolytic anemia due to a disorder of glycolytic enzymes": "Orphanet:98372", "Ovarian Granulosa Cell Tumor": "EFO:1000421", "DK1-CDG": "Orphanet:91131", "Disorder of mineral absorption and transport": "Orphanet:309836", "C-X-C motif chemokine 11 measurement": "EFO:0008057", "Autosomal dominant deafness-onychodystrophy syndrome": "Orphanet:79499", "Atypical hemolytic-uremic syndrome with C3 anomaly": "Orphanet:93575", "Anodontia": "Orphanet:99797", "Shaken Baby Syndrome": "EFO:1001423", "hematocrit": "EFO:0004348", "Methylmalonic acidemia with homocystinuria, type cblX": "Orphanet:369962", "renal cell adenocarcinoma": "EFO:0005708", "HNT-34": "EFO:0006583", "RWPE2": "EFO:0007610", "Odonto-onycho-dermal dysplasia": "Orphanet:2721", "CD71-negative, GlyA-positive orthochromatic erythroblast": "CL:0002018", "Isolated thyroid-stimulating hormone deficiency": "Orphanet:90674", "Genetic intestinal disease": "Orphanet:165655", "Femoral agenesis/hypoplasia, bilateral": "Orphanet:295067", "HCC1007": "EFO:0001168", "Encephalopathy due to prosaposin deficiency": "Orphanet:139406", "Congenital factor XI deficiency": "Orphanet:329", "Spheroid body myopathy": "Orphanet:268129", "Moraxella catarrhalis": "NCBITaxon:480", "VT847": "EFO:0004064", "Citrin deficiency": "Orphanet:247582", "Autosomal dominant non-syndromic intellectual disability": "Orphanet:178469", "NTera2 derived dopaminergic neuronal like cells": "EFO:0002961", "Acinetobacter infectious disease": "EFO:1000792", "Familial renal amyloidosis due to Apolipoprotein AII variant": "Orphanet:238269", "Familial vesicoureteral reflux": "Orphanet:289365", "Rare genetic palpebral, lacrimal system and conjunctival disease": "Orphanet:183598", "Spinocerebellar ataxia type 2": "Orphanet:98756", "caudal": "EFO:0001908", "optic neuritis": "EFO:0007405", "Malignant Ovarian Brenner Tumor": "EFO:1000357", "fisetin": "CHEBI:42567", "antispasmodic": "CHEBI:53784", "Early-onset ataxia with dementia": "Orphanet:98539", "eye": "UBERON:0000970", "tetralogy of fallot": "HP:0001636", "visual perception": "GO:0007601", "Ts-1": "EFO:0006963", "immature single positive thymocyte": "CL:0000805", "acetaldehyde": "CHEBI:15343", "Lung Abscess": "EFO:1001362", "epithelial cell": "CL:0000066", "AG04147 {http": "CLO:0034780", "Klippel-Trenaunay syndrome": "EFO:0007334", "267B1": "EFO:0001080", "17q21.31 microdeletion syndrome": "Orphanet:363958", "Secreted frizzled-related protein 3 measurement": "EFO:0008277", "ovarian leiomyosarcoma": "EFO:0006718", "Ovarian Choriocarcinoma": "EFO:1000413", "Congenital fibrinogen deficiency": "Orphanet:335", "Snowflake vitreoretinal degeneration": "Orphanet:91496", "Genetic neuromuscular junction disease": "Orphanet:98495", "AG10049 {http": "CLO:0021875", "mid cerebral vein": "UBERON:2005010", "cell proliferation": "GO:0008283", "Staphylococcus haemolyticus": "NCBITaxon:1283", "NCI-H1944": "EFO:0006667", "Female infertility due to gonadal dysgenesis": "Orphanet:399877", "Trialeurodes vaporariorum": "NCBITaxon:88556", "femur fracture": "EFO:0008553", "Vitis sp. cv. 'Norton'": "NCBITaxon:171960", "cotyledon adaxial epidermis": "PO:0006058", "Bartholin Gland Carcinoma": "EFO:1000103", "GM10833 {http": "CLO:0023795", "heparin cofactor 2 measurement": "EFO:0008150", "coccidiosis": "EFO:0007212", "angina pectoris": "EFO:0003913", "energy expenditure": "EFO:0005109", "response to low sodium diet": "EFO:0005402", "Autosomal dominant Robinow syndrome": "Orphanet:3107", "Ataxia-deafness-intellectual disability syndrome": "Orphanet:1188", "genetic modification": "EFO:0000510", "excreta": "UBERON:0000174", "66cl4": "EFO:0002038", "Multiple non-ossifying fibromatosis": "Orphanet:2029", "Congenital absence/hypoplasia of fingers excluding thumb, bilateral": "Orphanet:295114", "social anxiety disorder": "EFO:1001917", "Autosomal recessive spastic paraplegia type 27": "Orphanet:101007", "Piriqueta cistoides subsp. caroliniana": "NCBITaxon:57329", "atrophic thyroiditis": "EFO:0006813", "MOLM-16": "EFO:0006652", "Rapid-onset dystonia-parkinsonism": "Orphanet:71517", "Polydactyly of a biphalangeal thumb, bilateral": "Orphanet:295146", "5PSeq": "EFO:0008648", "Disorder of melanin metabolism": "Orphanet:352728", "Denys-Drash syndrome": "Orphanet:220", "Ovarian Carcinosarcoma": "EFO:1000412", "ML-DmD9": "EFO:0005833", "Cystic Kidney Disease": "EFO:0008615", "elongating embryo Ce": "EFO:0005506", "Talo-patello-scaphoid osteolysis": "Orphanet:50809", "olfactory system": "UBERON:0005725", "R8": "EFO:0001230", "Cervical Metaplasia": "EFO:1000168", "GM14535 {http": "CLO:0031600", "NCI-H1299": "EFO:0003043", "single-organism process": "GO:0044699", "posterior lateral line neuromast": "UBERON:2000940", "cystitis": "EFO:1000025", "Clostridium difficile 630": "NCBITaxon:272563", "Hepatic veno-occlusive disease - immunodeficiency": "Orphanet:79124", "response to trastuzumab": "EFO:0008347", "presumptive forebrain": "UBERON:0006240", "Partial bilateral aplasia of the M\u00c3\u00bcllerian ducts": "Orphanet:180068", "sialadenitis": "EFO:1001179", "Hyperglycinuria {http": "HP:0003108", "GM12814": "EFO:0001157", "lymph": "UBERON:0002391", "snRNA": "SO:0000274", "metastasis free survival": "EFO:0004919", "cardiotoxicity": "EFO:1001482", "splenic macrophage": "CL:0000871", "Autosomal dominant Charcot-Marie-Tooth disease type 2A1": "Orphanet:99946", "wellbeing measurement": "EFO:0007869", "Fagus sylvatica": "NCBITaxon:28930", "Teleopsis thaii": "NCBITaxon:346187", "oppositional defiant disorder": "HP:0010865", "cutaneous psoriasis measurement": "EFO:0007773", "susceptibility to bacterial meningitis measurement": "EFO:0008411", "cutaneous lupus erythematosus": "EFO:0003834", "CD38-high pre-BCR positive cell": "CL:0002051", "His bundle tachycardia": "Orphanet:3283", "Acropora palmata": "NCBITaxon:6131", "Transient tyrosinemia of the newborn": "Orphanet:3402", "Bilateral multicystic dysplastic kidney": "Orphanet:97364", "aluminium trichloride": "CHEBI:30114", "Isolated cryptophthalmia": "Orphanet:91396", "response to antineoplastic agent": "GO:0097327", "Acrodynia": "EFO:1001756", "alcohol drinking": "EFO:0004329", "PC-14": "EFO:0002844", "presumptive rhombomere 6": "UBERON:0007293", "Staphylococcus aureus subsp. aureus MRSA252": "NCBITaxon:282458", "liver disease": "EFO:0001421", "Autosomal recessive spastic paraplegia type 67": "Orphanet:401820", "gastrocnemius": "UBERON:0001388", "Alpha-thalassemia": "Orphanet:846", "D-serine": "CHEBI:16523", "GM23338": "EFO:0007950", "total ventricular volume measurement": "EFO:0007602", "FEV change measurement": "EFO:0005921", "DLD1": "EFO:0006389", "Aspergillus parasiticus": "NCBITaxon:5067", "46,XY ovotesticular disorder of sex development": "Orphanet:325345", "iberin": "EFO:0002671", "shoulder impingement syndrome": "EFO:1001178", "Wiedemann-Steiner syndrome": "Orphanet:319182", "MDCC-MSB1": "EFO:0002659", "pharyngula high-pec": "EFO:0001311", "Brachydactyly of fingers": "Orphanet:294996", "DNase-Hypersensitivity seq": "EFO:0003752", "whole genome shotgun sequencing": "EFO:0003744", "MDAMB157": "EFO:0001206", "Northern and Western European": "EFO:0004901", "Immunodeficiency due to a complement cascade protein anomaly": "Orphanet:101992", "postnatal": "EFO:0002948", "Microcephaly - cardiomyopathy": "Orphanet:2515", "colchicine": "CHEBI:23359", "sn-glycerol 3-phosphate": "CHEBI:15978", "plasma protease C1 inhibitor measurement": "EFO:0008261", "reproductive behaviour measurement": "EFO:0007862", "root epidermis {http": "PO:0006036", "Congenital cataract - progressive muscular hypotonia - hearing loss - developmental delay": "Orphanet:330054", "ancylostomiasis": "EFO:0007145", "PIP-Seq": "EFO:0008862", "interspecies interaction between organisms": "GO:0044419", "Upington disease": "Orphanet:3408", "GM17277 {http": "CLO:0013208", "empyema": "EFO:0003097", "Langerhans cell": "CL:0000453", "Transient neonatal diabetes mellitus": "Orphanet:99886", "bone fracture related measurement": "EFO:0004516", "Vibrio parahaemolyticus": "NCBITaxon:670", "SKO007": "EFO:0002339", "Estrogen resistance syndrome": "EFO:0009042", "enol-phenylpyruvate {http": "CHEBI:16815", "postcholecystectomy syndrome": "EFO:1001117", "Structure-Seq": "EFO:0008955", "Osteochondritis": "HP:0040188", "Multiple polyglandular tumor": "Orphanet:100094", "Short philtrum {http": "HP:0000322", "migraine with aura": "EFO:0005295", "coumarin": "CHEBI:28794", "gastric carcinoma": "EFO:0000178", "Heart defects - limb shortening": "Orphanet:1354", "Intermediate severe Salla disease": "Orphanet:309331", "larynx": "UBERON:0001737", "gastric non-cardia carcinoma": "EFO:0008502", "serine protease 27 measurement": "EFO:0008280", "Kidney Cyst": "EFO:1000313", "Anaeromyxobacter dehalogenans 2CP-C": "NCBITaxon:290397", "Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency": "Orphanet:209902", "Hyperphalangy, bilateral": "Orphanet:295142", "Hereditary angioedema type 3": "Orphanet:100054", "phenothiazine antipsychotic drug": "CHEBI:37930", "Aplasia cutis - myopia": "Orphanet:1117", "Genetic overgrowth/obesity syndrome": "Orphanet:183573", "HELP-Seq": "EFO:0008761", "Lethal congenital contracture syndrome": "Orphanet:294965", "MARIO": "EFO:0008795", "Salt-and-pepper syndrome": "Orphanet:370938", "Filippi syndrome": "Orphanet:3255", "Isolated dystonia": "Orphanet:156159", "longissimus thoracic muscle {http": "UBERON:0001401", "Ixodes scapularis": "NCBITaxon:6945", "Albinism-deafness syndrome": "Orphanet:998", "adhesion molecule measurement": "EFO:0004522", "Langerhans Cell Histiocytosis": "EFO:1000318", "alloimmunization": "EFO:0006804", "preadipocyte": "CL:0002334", "diabetic foot": "EFO:1001459", "Congenital genu recurvatum": "Orphanet:295229", "Lymphedema - distichiasis": "Orphanet:33001", "NS-seq": "EFO:0008831", "Fraction C precursor B cell": "CL:0002049", "Periodic paralysis with later-onset distal motor neuropathy": "Orphanet:397750", "Tuberculosis, Cutaneous": "EFO:1001443", "abnormality of the skin": "HP:0000951", "Penicillium corylophilum": "NCBITaxon:70792", "suicidal ideation": "EFO:0004320", "hyomandibular cartilage": "UBERON:0011607", "response to drug": "GO:0042493", "Bipartite talus": "Orphanet:364198", "ADULT syndrome": "Orphanet:978", "Plasmodium falciparum 3D7": "NCBITaxon:36329", "Subcutaneous neurofibromas {http": "HP:0100698", "virologic response measurement": "EFO:0006906", "WB-F344": "EFO:0002871", "sulfonyldimethane {http": "CHEBI:9349", "Autosomal recessive limb-girdle muscular dystrophy type 2P": "Orphanet:280333", "amyloid plaque accumulation rate": "EFO:0007646", "development or differentiation design": "EFO:0001746", "Infantile cerebellar-retinal degeneration": "Orphanet:313850", "mature CD1a-positive Langerhans cell": "CL:0001017", "protonema {http": "PO:0030003", "autism spectrum disorder": "EFO:0003756", "CIP-TAP": "EFO:0008688", "arteriolosclerosis": "EFO:1000819", "cotinine glucuronidation measurement": "EFO:0006508", "linoleate {http": "CHEBI:30245", "M059K": "EFO:0006451", "blastema": "UBERON:0005306", "benzene": "CHEBI:16716", "Triple A syndrome": "Orphanet:869", "lipoteichoic Acid": "CHEBI:28640", "Cardiodysrhythmic potassium-sensitive periodic paralysis": "Orphanet:37553", "Appendix Adenocarcinoma": "EFO:1000088", "embryo Ce": "WBls:0000003", "Familial progressive cardiac conduction defect": "Orphanet:871", "tyrosine-protein kinase receptor Tie-1, soluble measurement": "EFO:0008312", "hypertension": "EFO:0000537", "cervical squamous cell carcinoma": "EFO:1000172", "3-(3-hydroxyphenyl)propanoate {http": "CHEBI:57277", "tricuspid valve prolapse": "EFO:1001218", "Turner syndrome due to structural X chromosome anomalies": "Orphanet:99413", "GM17843 {http": "CLO:0016458", "Crouzon syndrome - acanthosis nigricans": "Orphanet:93262", "Tetrasomy 5p": "Orphanet:3309", "Fungi {http": "NCBITaxon:4751", "Pelizaeus-Merzbacher disease": "Orphanet:702", "breast invasive ductal carcinoma cell": "BTO:0002844", "NL2099": "EFO:0004062", "Streptococcus sp. 'group A'": "NCBITaxon:36470", "KMS-26": "EFO:0006615", "minocycline": "CHEBI:50694", "Hs 695T": "EFO:0006588", "antigen profiling": "EFO:0000747", "Palmoplantar keratoderma - XX sex reversal - predisposition to squamous cell carcinoma": "Orphanet:85112", "Situs inversus totalis": "Orphanet:101063", "Familial encephalopathy with neuroserpin inclusion bodies": "Orphanet:85110", "mouse prenatal": "EFO:0002543", "interleukin-22 (Homo sapiens)": "EFO:0003810", "Wernicke-Korsakoff syndrome": "EFO:1001242", "intravenous anaesthetic": "CHEBI:38877", "interleukin 15 receptor subunit alpha measurement": "EFO:0008172", "O-tetradecanoyl-L-carnitine {http": "CHEBI:84634", "Myopathy - growth delay - intellectual disability - hypospadias": "Orphanet:2601", "CAL 27": "EFO:0006366", "Amelogenesis imperfecta - nephrocalcinosis": "Orphanet:1031", "DNaseI-Seq": "EFO:0008717", "Caenorhabditis component": "EFO:0005496", "Phytophthora infestans": "NCBITaxon:4787", "chromophobe adenoma": "EFO:1000867", "Reunion Island's Larsen syndrome": "Orphanet:294049", "Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency": "Orphanet:397593", "posterior lateral line ganglion": "UBERON:2001314", "Malignant migrating partial seizures of infancy": "Orphanet:293181", "South Texas Assessment of Neurocognition": "EFO:0004785", "Non-ST Elevation Myocardial Infarction": "EFO:0008586", "postcentral gyrus": "UBERON:0002581", "Drosophila melanogaster cell line": "EFO:0002935", "plant structure development stage": "PO:0009012", "Salivary Gland Small Cell Carcinoma": "EFO:1000519", "Timothy syndrome": "Orphanet:65283", "dumping syndrome": "EFO:1001307", "mature interstitial dendritic cell": "CL:0001013", "percent": "UO:0000187", "primitive reticulocyte": "CL:0002356", "CBA/CaJ": "EFO:0001336", "Idiopathic hypercalciuria": "Orphanet:2197", "PLCG2-associated antibody deficiency and immune dysregulation": "Orphanet:300359", "Hypoxanthine-guanine phosphoribosyltransferase deficiency": "Orphanet:206428", "Ovarian Small Cell Carcinoma": "EFO:1000431", "scTHS-seq": "EFO:0008915", "Disorder of O-xylosylglycan synthesis": "Orphanet:309450", "neutrophil progenitor cell": "CL:0000834", "pyramidal cell": "CL:0000598", "cerebral hemisphere": "UBERON:0001869", "Aromatase excess syndrome": "Orphanet:178345", "Paris-Trousseau thrombocytopenia": "Orphanet:851", "Partial deletion of the long arm of chromosome 16": "Orphanet:262128", "homocitrate (2-) {http": "CHEBI:36458", "reaction time measurement": "EFO:0008393", "GM17171 {http": "CLO:0014024", "Familial renal amyloidosis due to fibrinogen A alpha-chain variant": "Orphanet:93562", "HDL cholesterol": "CHEBI:47775", "Meacham syndrome": "Orphanet:3097", "pelvic organ prolapse": "EFO:0004710", "phenytoin": "CHEBI:8107", "Distal trisomy 11q": "Orphanet:96103", "monocyte early outgrowth colony forming unit": "EFO:0004506", "GM15029 {http": "CLO:0030305", "inflammatory breast carcinoma": "EFO:1000984", "Benign recurrent intrahepatic cholestasis": "Orphanet:65682", "embryonic stage 17": "EFO:0005877", "ploidy": "PATO:0001374", "Paracoccidioides brasiliensis Pb01": "NCBITaxon:502779", "YKL40 measurement": "EFO:0004869", "hypogastrium": "UBERON:0013203", "Churg-Strauss syndrome": "EFO:0007208", "hypertrophic cardiomyopathy": "EFO:0000538", "childhood acute monocytic leukemia": "EFO:1001944", "trans-16": "EFO:0006822", "cerebrospinal fluid otorrhea": "EFO:1001775", "brain development": "GO:0007420", "Tuberous sclerosis": "Orphanet:805", "scleredema adultorum": "EFO:1000762", "velocity of sound measurement": "EFO:0005654", "Lissencephaly due to TUBA1A mutation": "Orphanet:171680", "drug dependence": "EFO:0003890", "SCI-seq": "EFO:0008908", "Pilodental dysplasia - refractive errors": "Orphanet:2892", "Combined oxidative phosphorylation defect type 23": "EFO:0009033", "basophil count": "EFO:0005090", "Autosomal recessive cerebral atrophy": "Orphanet:363969", "Familial primary hypomagnesemia with normocalcuria": "Orphanet:306522", "Dysplasia epiphysealis hemimelica": "Orphanet:1822", "C3H/HeOuJ": "EFO:0007833", "breast ductal adenocarcinoma": "EFO:0006318", "CD1 mus strain": "EFO:0005180", "TP53 Positive Breast Carcinoma": "EFO:1002010", "Autosomal recessive optic atrophy, OPA7 type": "Orphanet:227976", "Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency": "Orphanet:90791", "acrolein": "CHEBI:15368", "Capsella rubella": "NCBITaxon:81985", "HCC70": "EFO:0001181", "GM00719": "EFO:0004922", "Cantrell pentalogy": "Orphanet:1335", "Radial hemimelia, unilateral": "Orphanet:295069", "ATC Code R Respiratory system": "EFO:0005645", "dorsal ridge": "UBERON:4200173", "Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7": "Orphanet:96182", "presumptive enteric nervous system": "UBERON:0006600", "Genetic hyperferritinemia without iron overload": "Orphanet:254704", "Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency": "Orphanet:248305", "duodenal benign neoplasm": "EFO:1000907", "Vitis vinifera": "NCBITaxon:29760", "Haemophilus ducreyi": "NCBITaxon:730", "Familial aortic dissection": "Orphanet:229", "CD4-positive, alpha-beta intraepithelial T cell": "CL:0000793", "paclitaxel": "CHEBI:45863", "alveolar macrophage": "CL:0000583", "Betula pendula": "NCBITaxon:3505", "Alphavirus infectious disease": "EFO:0007142", "lichen planus": "EFO:1000726", "medical procedure": "EFO:0002571", "Ovarian Germ Cell Tumor": "EFO:1000419", "Basaloid Carcinoma": "EFO:1000105", "genotyping": "EFO:0000750", "myoclonic cerebellar dyssynergia": "EFO:1001053", "Usher syndrome type 2": "Orphanet:231178", "ILSXISS56/TejJ": "EFO:0002989", "characterization of functional areas of human genome": "EFO:0002912", "Rattus": "NCBITaxon:10114", "refractory anemia": "EFO:0003802", "Woodhouse-Sakati syndrome": "Orphanet:3464", "Okihiro syndrome due to 20q13 microdeletion": "Orphanet:261638", "response to platinum based chemotherapy": "EFO:0004647", "leprosy": "EFO:0001054", "Angiolipoma": "EFO:1000085", "Scleroderma Polymyositis Overlap Syndrome": "EFO:1001994", "purine nucleoside metabolic process": "GO:0042278", "His-Ala {http": "CHEBI:73924", "pathologic complete response measurement": "EFO:0007771", "NCI-H630": "EFO:0002297", "retinoic acid": "CHEBI:26536", "primary Haemophilus infectious disease": "EFO:1001127", "osteochondrodysplasia": "EFO:0005571", "YCC16": "EFO:0002879", "metamphetamine dependence": "EFO:0004701", "nucleoside triphosphate metabolic process": "GO:0009141", "Multifocal pattern dystrophy simulating fundus flavimaculatus": "Orphanet:99003", "myeloid cell": "CL:0000763", "Severe intellectual disability and progressive spastic paraplegia": "Orphanet:280763", "heterocycle biosynthetic process": "GO:0018130", "salivary gland neoplasm": "EFO:0003826", "Thiamine-responsive maple syrup urine disease": "Orphanet:268184", "vitamin D deficiency": "EFO:0003762", "heregulin B1": "EFO:0003308", "GM17238 {http": "CLO:0014332", "HCC1159": "EFO:0003127", "Neuroectodermal-endocrine syndrome": "Orphanet:2676", "Aniridia - absent patella": "Orphanet:1069", "wild-derived inbred strain": "EFO:0004010", "abnormality of the aorta": "HP:0001679", "Goto-Kakizaki": "EFO:0000179", "braces": "EFO:0004291", "response to dietary potassium supplementation": "EFO:0005403", "GM17842 {http": "CLO:0016457", "trans-4-hydroxy-L-proline betaine {http": "CHEBI:85533", "GM17825 {http": "CLO:0016517", "Stenotrophomonas maltophilia": "NCBITaxon:40324", "trigeminal neural crest": "UBERON:0005563", "Downslanted palpebral fissures {http": "HP:0000494", "cerebral ventricle cancer": "EFO:0007201", "frontal cortex": "UBERON:0001870", "Euglenozoa Infections": "EFO:1001319", "testosterone": "CHEBI:17347", "palatine tonsil": "UBERON:0002373", "thyroid volume": "EFO:0004865", "International Unit per milliliter": "EFO:0002928", "Focal acral hyperkeratosis": "Orphanet:308013", "GM11830": "EFO:0001118", "Smith-McCort dysplasia": "Orphanet:178355", "breast adenocarcinoma": "EFO:0000304", "epiblast cell": "CL:0000352", "2-aminoadipic 2-oxoadipic aciduria": "Orphanet:79154", "localised cicatricial pemphigoid": "EFO:0008611", "episodic memory": "EFO:0004333", "Glucose-galactose malabsorption": "Orphanet:35710", "Mono Mac 6": "EFO:0006287", "Autosomal dominant spastic paraplegia type 38": "Orphanet:171617", "Zymoseptoria tritici": "NCBITaxon:1047171", "T47D": "EFO:0001247", "Dictyocaulus infectious disease": "EFO:0007235", "glycoprotein measurement": "EFO:0004555", "folic acid transport": "GO:0015884", "HCC0630": "EFO:0006421", "melanoacanthoma": "EFO:1000733", "Dermochondrocorneal dystrophy": "Orphanet:79149", "Laccaria bicolor S238N-H82": "NCBITaxon:486041", "Developmental delay - deafness, Hildebrand type": "Orphanet:163988", "functional impairment measurement": "EFO:0005412", "ankle joint": "UBERON:0001488", "Cabbage leaf curl virus {http": "NCBITaxon:51336", "Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia": "Orphanet:632", "Langer mesomelic dysplasia": "Orphanet:2632", "Polymalformative genetic syndrome with increased risk of developing cancer": "Orphanet:183422", "T0 stage": "EFO:0004937", "Fallot complex - intellectual disability - growth delay": "Orphanet:3304", "vitamin measurement": "EFO:0004729", "Unilateral polymicrogyria": "Orphanet:268943", "Partial deletion of the short arm of chromosome 6": "Orphanet:261902", "primary Bacillaceae infectious disease": "EFO:1001124", "ND00268 {http": "CLO:0026399", "Marie Unna hereditary hypotrichosis": "Orphanet:444", "Lipowiec ecotype": "EFO:0007607", "pons": "UBERON:0000988", "amiodarone": "CHEBI:2663", "Nasonia vitripennis": "NCBITaxon:7425", "B cell derived cell line": "EFO:0001640", "Rectal Traditional Serrated Adenoma": "EFO:1000503", "hippocampus": "MA:0000191", "digit length ratio": "EFO:0004841", "Multiple epiphyseal dysplasia, Al-Gazali type": "Orphanet:166024", "response to antipsychotic drug": "GO:0097332", "Dupuytren Contracture": "EFO:0004229", "Macrodactyly of fingers, bilateral": "Orphanet:295241", "carbon dioxide": "CHEBI:16526", "Duvenhage virus": "NCBITaxon:38767", "Trichomonas vaginitis": "EFO:0007521", "cell suspension culture": "BTO:0000221", "NC-NC": "EFO:0007115", "Rhodococcus jostii": "NCBITaxon:132919", "NCI-H2882": "EFO:0003121", "blood": "UBERON:0000178", "panniculitis": "EFO:1000746", "Circoviridae Infections": "EFO:1001292", "blood copper measurement": "EFO:0007578", "pemphigus vegetans": "EFO:0008613", "breast adenocarcinoma cell line": "EFO:0005215", "DSM-IV-based social scale": "EFO:0004780", "Trisomy 17p": "Orphanet:261290", "Seq-Well": "EFO:0008919", "pathological": "PATO:0001869", "Blepharophimosis-intellectual disability syndrome": "Orphanet:293642", "GM17170 {http": "CLO:0014022", "Haddad syndrome": "Orphanet:99803", "N-hexanoylglycine {http": "CHEBI:64390", "Darwin's tubercule": "EFO:0007674", "acne": "EFO:0003894", "thyroid gland": "UBERON:0002046", "Other syndrome with lissencephaly as a major feature": "Orphanet:102010", "topiramate": "CHEBI:63631", "nasal and broncial associated lymphoid tissue macrophage": "CL:0000886", "Congenital upper palpebral retraction": "Orphanet:98579", "terminal ileum": "EFO:0005185", "Malignant Paraganglioma": "EFO:1000360", "C3A": "EFO:0002121", "Bile acid synthesis defect with cholestasis and malabsorption": "Orphanet:163631", "docosapentaenoate {http": "CHEBI:78053", "Cleft mandible": "HP:0010752", "NAN 190 hydrobromide": "CHEBI:64123", "Prunus persica": "NCBITaxon:3760", "Catecholaminergic polymorphic ventricular tachycardia": "Orphanet:3286", "Thiamine deficiency": "EFO:0008569", "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency": "Orphanet:90795", "BruChase-Seq": "EFO:0008662", "Eye Burns": "EFO:1001788", "Reye syndrome": "EFO:0007467", "J1": "EFO:0004990", "X-linked agammaglobulinemia": "Orphanet:47", "Abnormality of the vasculature": "HP:0002597", "iPS DF 6.9": "EFO:0007098", "Congenital absence of thigh and lower leg with foot present, unilateral": "Orphanet:295089", "anti-IgG": "EFO:0005030", "Hemoglobinopathy": "Orphanet:68364", "nitrofurantoin": "CHEBI:71415", "oculomotor nuclear complex": "UBERON:0001715", "transport vesicle": "GO:0030133", "Linear nevus sebaceus syndrome": "Orphanet:2612", "Hypoparathyroidism - deafness - renal disease": "Orphanet:2237", "early whole plant fruit ripening stage {http": "PO:0007001", "paracetamol sulfate {http": "CHEBI:32635", "mature basophil": "CL:0000043", "Hordeum vulgare": "NCBITaxon:4513", "cranial nerve malignant neoplasm": "EFO:1000884", "Hereditary elliptocytosis": "Orphanet:288", "ARX-related epileptic encephalopathy": "Orphanet:182079", "Usual Ductal Breast Hyperplasia": "EFO:1000612", "Uveal coloboma - cleft lip and palate - intellectual disability": "Orphanet:1473", "Hypohidrotic ectodermal dysplasia with immunodeficiency": "Orphanet:98813", "GM15224 {http": "CLO:0027484", "Rare female infertility due to an anomaly of ovarian function of genetic origin": "Orphanet:400022", "Togaviridae infectious disease": "EFO:0007513", "X-linked erythropoietic protoporphyria": "EFO:0009064", "Staphylococcus aureus subsp. aureus MSSA476": "NCBITaxon:282459", "endometrial stromal tumor": "EFO:1000920", "myoblast cell line": "BTO:0000256", "Hyperlysinemia": "Orphanet:2203", "Congenital intestinal motility disorder": "Orphanet:104009", "Macrodactyly of fingers": "Orphanet:295044", "Rectal Villous Adenoma": "EFO:1000506", "Colobomatous microphthalmia": "Orphanet:98938", "minor histocompatibility congenic strain": "EFO:0000368", "Encephalitis, Tick-Borne": "EFO:1001309", "Hirschsprung disease - type D brachydactyly": "Orphanet:2150", "messenger RNA": "CHEBI:33699", "Marfanoid habitus - inguinal hernia - advanced bone age": "Orphanet:314041", "epicondylitis": "EFO:1001887", "Sus scrofa": "NCBITaxon:9823", "response to alcohol": "EFO:0005526", "Pasteurellaceae Infections": "EFO:1001386", "HMEC1": "EFO:0005383", "parasitic infection": "EFO:0001067", "Hydrocephalus - obesity - hypogonadism": "Orphanet:2183", "GM12750": "EFO:0001149", "drug hypersensitivity sydrome": "EFO:1002004", "Split hand": "Orphanet:294992", "Chronic diarrhea due to glucoamylase deficiency": "Orphanet:103907", "sensillum": "UBERON:0002536", "Medicago sativa": "NCBITaxon:3879", "oligonucleotide synthesizer": "OBI:0400113", "14q11.2 microdeletion syndrome": "Orphanet:261120", "Callithrix jacchus": "NCBITaxon:9483", "Streptomyces clavuligerus": "NCBITaxon:1901", "bipolar disorder": "EFO:0000289", "epiGBS": "EFO:0008732", "Calcifying Fibrous Tumor": "EFO:1000148", "pancreaticobiliary malunion": "EFO:0006886", "rhombomere 2 floor plate": "UBERON:0005570", "rickets": "EFO:0005583", "Sarcophaga crassipalpis": "NCBITaxon:59312", "RNAi profiling by array": "EFO:0001030", "Occipital horn syndrome": "Orphanet:198", "Ophthalmoplegia - intellectual disability - lingua scrotalis": "Orphanet:2743", "snoring measurement": "EFO:0008341", "internal ear": "UBERON:0001846", "Taurodontia - absent teeth - sparse hair": "Orphanet:2731", "GM17791 {http": "CLO:0016675", "hypothalamus": "UBERON:0001898", "Frankia alni ACN14a": "NCBITaxon:326424", "GM17146 {http": "CLO:0013942", "nephron tubule": "UBERON:0001231", "combined partial 17-alpha-hydroxylase/17,20-lyase deficiency": "EFO:0009067", "trichinosis": "EFO:0007520", "RRBS": "EFO:0008900", "instrument design": "EFO:0001451", "cervical carcinoma cell line": "EFO:0005218", "signaling receptor activity": "GO:0038023", "interventricular septum": "UBERON:0002094", "Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome": "Orphanet:314394", "Goldblatt syndrome": "Orphanet:166272", "N-allyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide": "CHEBI:64002", "Macrocephaly-autism syndrome": "Orphanet:210548", "Disorder of carnitine cycle and carnitine transport": "Orphanet:309130", "trichloroethylene-induced hypersensitivity": "EFO:0007685", "Enterococcus hirae": "NCBITaxon:1354", "Escherichia coli UTI89": "NCBITaxon:364106", "Acetazolamide-responsive myotonia": "Orphanet:99736", "Partial duplication of the long arm of chromosome 19": "Orphanet:262986", "Metaphyseal chondrodysplasia, Kaitila type": "Orphanet:166038", "Recessive dystrophic epidermolysis bullosa-generalized other": "Orphanet:89842", "CS57618": "EFO:0000035", "analyte role": "OBI:0000275", "Joubert syndrome with Jeune asphyxiating thoracic dystrophy": "Orphanet:397715", "Neonatal diabetes mellitus": "Orphanet:224", "immature Vgamma2-positive fetal thymocyte": "CL:0002378", "KARPAS 231": "EFO:0005389", "type 1 diabetes nephropathy": "EFO:0004996", "seed structure": "EFO:0000991", "Parotid Gland Pleomorphic Adenoma": "EFO:1000462", "monokine induced by gamma interferon measurement": "EFO:0008236", "HCC1419": "EFO:0005372", "Congenital bile acid synthesis defect type 4": "Orphanet:79095", "Xanthomonas oryzae pv. oryzicola {http": "NCBITaxon:129394", "MPE-seq": "EFO:0008821", "Soft Tissue Neoplasm": "EFO:1000541", "Lipodystrophy due to peptidic growth factors deficiency": "Orphanet:1979", "Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism": "Orphanet:2250", "age at alcohol diagnosis": "EFO:0005602", "SK-N-SH_RA": "EFO:0002802", "Familial cerebral saccular aneurysm": "Orphanet:231160", "mean arterial pressure": "EFO:0006340", "Beta-thalassemia - X-linked thrombocytopenia": "Orphanet:231393", "Rare metabolic liver disease": "Orphanet:101940", "CW-2": "EFO:0006560", "phase-transfer catalyst role": "CHEBI:63060", "SK-MEL-31": "EFO:0006489", "urogenital tuberculosis": "EFO:0007531", "HUES1": "EFO:0005355", "non-Hodgkins lymphoma": "EFO:0005952", "Craniosynostosis - Dandy-Walker malformation - hydrocephalus": "Orphanet:1538", "Non-polyposis Turcot syndrome": "Orphanet:99817", "brachial circumference": "EFO:0004589", "Rare conjunctival disease": "Orphanet:98610", "interleukin-1 beta (Mus musculus)": "EFO:0003795", "Microcephalic osteodysplastic dysplasia, Saul-Wilson type": "Orphanet:85172", "Beckwith-Wiedemann syndrome due to CDKN1C mutation": "Orphanet:231120", "Disorder of iron metabolism and transport": "Orphanet:309842", "motion sickness": "EFO:0006928", "Hereditary sensory and autonomic neuropathy type 4": "Orphanet:642", "Secretory Meningioma": "EFO:1000522", "hyperandrogenism": "EFO:0009006", "Uveal Melanoma": "EFO:1000616", "Abetalipoproteinemia": "Orphanet:14", "taurochenodeoxycholate {http": "CHEBI:9407", "upper aerodigestive tract neoplasm": "EFO:0004284", "Cat-eye syndrome": "Orphanet:195", "GM17127 {http": "CLO:0015126", "odontoclast": "CL:0000588", "SNU387": "EFO:0002346", "Influenza A virus (A/Texas/36/1991(H1N1))": "NCBITaxon:380964", "response to sulfasalazine": "EFO:0008324", "O-isobutyrylcarnitine {http": "CHEBI:73017", "Athyreosis": "Orphanet:95713", "perivascular macrophage": "CL:0000881", "ethambutol": "CHEBI:4877", "polyradiculoneuropathy": "EFO:1001116", "GM12716": "EFO:0001147", "MCF-7": "EFO:0001203", "Unilateral renal agenesis": "Orphanet:93100", "Neisseria polysaccharea": "NCBITaxon:489", "Cardiocranial syndrome, Pfeiffer type": "Orphanet:2872", "Bilateral striopallidodentate calcinosis": "Orphanet:1980", "CCRF-SB": "EFO:0006550", "17q12 microduplication syndrome": "Orphanet:261272", "part per million": "UO:0000169", "GM17243 {http": "CLO:0014413", "GM17104 {http": "CLO:0014900", "medial octavolateralis nucleus": "UBERON:2000291", "high altitude pulmonary edema": "EFO:1002002", "NCI-H1975": "EFO:0002271", "ADHD symptom measurement": "EFO:0007860", "Aplasia of lacrimal and salivary glands": "Orphanet:86815", "diabetes mellitus": "EFO:0000400", "T-B+ severe combined immunodeficiency due to gamma chain deficiency": "Orphanet:276", "angiostatin measurement": "EFO:0008024", "Bardet-Biedl syndrome 12": "EFO:0009023", "GM17198 {http": "CLO:0013823", "Mucor circinelloides": "NCBITaxon:36080", "piperonylbutoxide": "CHEBI:32687", "HGC-27": "EFO:0006581", "Reticulate acropigmentation of Kitamura": "Orphanet:178307", "Tetrasomy 9p": "Orphanet:3310", "Disorder of vitamin and non-protein cofactor absorption and transport\u00c2": "Orphanet:309827", "weight percent": "EFO:0002904", "staphyloenterotoxemia": "EFO:0007497", "ganglioglioma": "EFO:0003094", "sodium dihydrogenphosphate": "CHEBI:37585", "alpha-carotene measurement": "EFO:0007893", "oral Crohn's disease": "EFO:0005625", "Pseudohypoparathyroidism type 1B": "Orphanet:94089", "MULIBREY nanism": "Orphanet:2576", "Salmonella enterica subsp. enterica serovar Heidelberg": "NCBITaxon:611", "subdural empyema": "EFO:1001196", "B\u00c3\u00b6\u00c3\u00b6k syndrome": "Orphanet:1262", "Pediococcus acidilactici": "NCBITaxon:1254", "praziquantel": "CHEBI:45267", "BLESS": "EFO:0008657", "Hematological disorder with renal involvement": "Orphanet:93614", "endothelial cell-selective adhesion molecule measurement": "EFO:0008120", "Grant syndrome": "Orphanet:2097", "X-linked intellectual disability, Hedera type": "Orphanet:93952", "SKMEL3": "EFO:0002333", "Chlamydotis undulata": "NCBITaxon:172680", "Skin fragility-woolly hair-palmoplantar keratoderma syndrome": "Orphanet:293165", "Gibberella pulicaris": "NCBITaxon:5128", "X-linked intellectual disability - hypotonic face": "Orphanet:73220", "Myopia": "HP:0000545", "Rare thrombotic disorder due to a constitutional platelet anomaly": "Orphanet:248401", "hydrochloric acid": "CHEBI:17883", "Cervical Mucinous Adenocarcinoma, Villoglandular Variant": "EFO:1000170", "setariasis": "EFO:0007482", "memory impairment": "EFO:0001072", "VH-64": "EFO:0002870", "pain agnosia": "EFO:1001484", "ICE": "EFO:0008773", "perfluorodecanoic acid": "CHEBI:35546", "nebivolol": "CHEBI:64022", "Keratosis follicularis - dwarfism - cerebral atrophy": "Orphanet:2339", "C-C motif chemokine 16 measurement": "EFO:0008044", "single organism signaling": "GO:0044700", "Syndromic oculocutaneous albinism": "Orphanet:284811", "cellular macromolecule metabolic process": "GO:0044260", "Palpebral nevus": "Orphanet:98588", "agarose": "CHEBI:2511", "Bilateral renal dysplasia": "Orphanet:93173", "Spondyloepiphyseal dysplasia, MacDermot type": "Orphanet:163668", "independent variable specification": "OBI:0000750", "Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature": "Orphanet:308031", "Plasmodium vivax malaria": "EFO:0007445", "Perlman syndrome": "Orphanet:2849", "HCC2279": "EFO:0006431", "B-lymphoblast": "EFO:0005293", "infantile hypertrophic pyloric stenosis": "EFO:0004707", "Tetraploidy": "Orphanet:3305", "Brain Stem Glioma": "EFO:1000142", "Axenfeld anomaly": "Orphanet:98978", "SNU475": "EFO:0002350", "neurohypophysis": "UBERON:0002198", "response to morphine": "GO:0043278", "MCF10DCIS.COM": "EFO:0006643", "D-penicillamine": "CHEBI:7959", "Ornithorhynchus anatinus": "NCBITaxon:9258", "Autosomal ichthyosis syndrome with prominent hair abnormalities": "Orphanet:281222", "thymic lymphoma": "EFO:1000054", "3 hr schistosomulum": "EFO:0007713", "Constitutional deficiency anemia": "Orphanet:248296", "vitamin metabolic disorder": "EFO:0005596", "Lissencephaly type 1 due to doublecortin gene mutation": "Orphanet:2148", "Mesocricetus auratus": "NCBITaxon:10036", "thyroxine": "CHEBI:30660", "Granular Cell Tumor": "EFO:1000284", "caudate nucleus volume": "EFO:0004830", "CS57904": "EFO:0000162", "Nervous system anomaly with eye involvement": "Orphanet:98692", "GM10847": "EFO:0005336", "ribose phosphate metabolic process": "GO:0019693", "Epidermophyton floccosum": "NCBITaxon:34391", "Rolandic epilepsy - paroxysmal exercise-induced dystonia - writer's cramp": "Orphanet:163727", "pleomorphic liposarcoma": "EFO:0003083", "Sensory ataxic neuropathy - dysarthria - ophthalmoparesis": "Orphanet:70595", "galectin-3 measurement": "EFO:0008137", "Oculocutaneous albinism type 1B": "Orphanet:79434", "ILSXISS79/TejJ": "EFO:0002992", "Alternariosis": "EFO:1001262", "immortal cell line cell": "CL:0000002", "Coxa Vara": "EFO:1001298", "Isochrysis galbana": "NCBITaxon:37099", "Disorder of fructose metabolism": "Orphanet:308463", "glycoursodeoxycholate {http": "CHEBI:132030", "600MPE": "EFO:0001085", "punctate palmoplantar keratoderma type III": "EFO:1000758", "adult eye primordium": "FBbt:10005249", "Dysostosis with combined reduction defects of upper and lower limbs": "Orphanet:294957", "Combined immunodeficiency due to ORAI1 deficiency": "Orphanet:317428", "U266": "EFO:0001254", "Multicentric carpo-tarsal osteolysis with or without nephropathy": "Orphanet:2774", "Lens size anomaly": "Orphanet:98652", "Brugia malayi": "NCBITaxon:6279", "Primary lymphedema": "Orphanet:77240", "N3 lymph node stage": "EFO:0004935", "Cryptopygus antarcticus": "NCBITaxon:187623", "anterior chamber depth measurement": "EFO:0005668", "response to dietary antigen": "EFO:0005844", "Rapidly progressive glomerulonephritis": "Orphanet:280569", "Metachromatic leukodystrophy, late infantile form": "Orphanet:309256", "Primary Pulmonary Diffuse Large B-Cell Lymphoma": "EFO:1000495", "Albright hereditary osteodystrophy": "Orphanet:665", "Multiple epiphyseal dysplasia and pseudoachondroplasia": "Orphanet:93429", "transverse colon": "UBERON:0001157", "aortic root size": "EFO:0005037", "acrokeratosis verruciformis": "EFO:1000666", "threonine {http": "CHEBI:26986", "Ehlers-Danlos syndrome, kyphoscoliotic type": "Orphanet:1900", "Salmonella enterica subsp. enterica serovar Thompson": "NCBITaxon:600", "Partial duplication of the long arm of chromosome 10": "Orphanet:262914", "methylmalonic aciduria and homocystinuria type cblE": "EFO:0005568", "fruit formation stage {http": "PO:0025501", "overactive bladder": "EFO:1000781", "Trisomy 9p": "Orphanet:236", "Malignant Mixed Neoplasm": "EFO:1000356", "SK-MEL-5": "EFO:0005720", "(2R,3S)-EHNA hydrochloride": "CHEBI:64139", "Melkersson-Rosenthal syndrome": "EFO:1001039", "Deafness -  small bowel diverticulosis - neuropathy": "Orphanet:3217", "Combined immunodeficiency due to DOCK8 deficiency": "Orphanet:217390", "Pfeiffer-Palm-Teller syndrome": "Orphanet:2871", "male germ cell": "CL:0000015", "Jeune syndrome": "Orphanet:474", "Morning glory syndrome": "Orphanet:35737", "CB4856": "EFO:0004055", "Maffucci syndrome": "Orphanet:163634", "HPV-associated cervical carcinoma": "EFO:1002015", "Familial anetoderma": "Orphanet:228277", "hexose measurement": "EFO:0007631", "Paracoccidioides brasiliensis": "NCBITaxon:121759", "N-Butyrylglycine {http": "CHEBI:89963", "Ehlers-Danlos syndrome, spondylocheirodysplastic type": "Orphanet:157965", "seasonal allergic rhinitis": "EFO:0003956", "azinomycin B": "CHEBI:50862", "endocrine pancreas": "UBERON:0000016", "treatment protocol": "EFO:0003969", "diabetes mellitus type 2 associated cataract": "EFO:0004596", "all-cis-icosa-5,8,11,14,17-pentaenoic acid": "CHEBI:28364", "psychosis predisposition measurement": "EFO:0008337", "methamphetamine": "CHEBI:6809", "A20": "EFO:0005285", "Gallus gallus": "NCBITaxon:9031", "Autosomal recessive limb-girdle muscular dystrophy type 2J": "Orphanet:140922", "Partial deletion of the long arm of chromosome 4": "Orphanet:262029", "Microcephaly - digital anomalies - intellectual disability": "Orphanet:137653", "DU 145": "EFO:0005441", "optic disc measurement": "EFO:0006936", "Continuous spikes and waves during sleep": "Orphanet:725", "Growth delay - hydrocephaly - lung hypoplasia": "Orphanet:3035", "spotted single stranded oligo reporter": "EFO:0005079", "Avulavirus infectious disease": "EFO:0007161", "coelomocyte": "CL:0000421", "Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen": "Orphanet:251279", "Hemolytic anemia due to glucophosphate isomerase deficiency": "Orphanet:712", "establishment of localization in cell": "GO:0051649", "PL45": "EFO:0006474", "GM17130 {http": "CLO:0015085", "calcitriol": "CHEBI:17823", "cystic lymphangioma": "EFO:1000888", "screening library": "EFO:0007559", "1q21.1 microduplication syndrome": "Orphanet:250994", "pharyngeal arch": "UBERON:0002539", "conjunctival pigmentation": "EFO:1000682", "T stage": "EFO:0004928", "Alveolar proteinosis": "HP:0006517", "Xeroderma pigmentosum complementation group C": "Orphanet:276255", "oleic acid measurement": "EFO:0006810", "soleus muscle": "UBERON:0001389", "neurointermediate lobe": "EFO:0002520", "HOMA-B": "EFO:0004469", "alcoholic neuropathy": "EFO:1000803", "Abnormality of the cardiovascular system": "HP:0001626", "GM17121 {http": "CLO:0015115", "sulfate {http": "CHEBI:16189", "coisogenic strain": "EFO:0004002", "material entity": "BFO:0000040", "X-linked corneal dermoid": "Orphanet:1661", "GM17802 {http": "CLO:0016495", "Urinary retention": "HP:0000016", "Lactobacillus frumenti": "NCBITaxon:104955", "Central areolar choroidal dystrophy": "Orphanet:75377", "Staphylococcus saprophyticus subsp. saprophyticus": "NCBITaxon:147452", "pancreatic neoplasm": "EFO:0003860", "Nijmegen breakage syndrome-like disorder": "Orphanet:240760", "Absence deformity of leg - cataract": "Orphanet:2310", "Bandrowski's base": "CHEBI:53109", "facial morphology measurement": "EFO:0007841", "male": "PATO:0000384", "Saccharum officinarum complex": "NCBITaxon:286192", "Autosomal recessive spastic paraplegia type 53": "Orphanet:319199", "Crisponi syndrome": "Orphanet:1545", "Truncal obesity {http": "HP:0001956", "Combined Lung Carcinoma": "EFO:1000200", "response to radiation": "GO:0009314", "preoptic area": "UBERON:0001928", "Deafness with labyrinthine aplasia, microtia, and microdontia": "Orphanet:90024", "docosatetranoic acid measurement": "EFO:0008357", "GM17255 {http": "CLO:0014395", "Hereditary spastic paraplegia": "Orphanet:685", "Neisseria gonorrhoeae F62": "NCBITaxon:528351", "Puumala virus": "NCBITaxon:11604", "AG13066 {http": "CLO:0022132", "hepatitis A virus cellular receptor 2 measurement": "EFO:0008151", "Zea mays subsp. mays": "NCBITaxon:381124", "Blepharoptosis - myopia - ectopia lentis": "Orphanet:1259", "Ataxia-telangiectasia": "Orphanet:100", "RNA stability design": "EFO:0001783", "lateral mesenchyme derived from mesoderm": "UBERON:0007683", "aortic arch": "UBERON:0004363", "aggressive": "EFO:0002752", "Paternal uniparental disomy of chromosome 6": "Orphanet:96191", "CD14-positive, CD16-negative classical monocyte": "CL:0002057", "Combined immunodeficiency due to STIM1 deficiency": "Orphanet:317430", "gallbladder neoplasm": "EFO:0004606", "eicosadienoic acid measurement": "EFO:0008359", "NCI-H720": "EFO:0002302", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency": "Orphanet:284282", "complement factor I measurement": "EFO:0008099", "GM14475 {http": "CLO:0031272", "environmental exposure measurement": "EFO:0008360", "SR": "EFO:0002352", "mouth floor": "UBERON:0003679", "Gerstmann-Straussler-Scheinker syndrome": "Orphanet:356", "mucocutaneous Leishmaniasis": "EFO:0007379", "Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome": "Orphanet:2698", "High anorectal malformation": "Orphanet:171201", "prion disease": "EFO:0004720", "array control label": "EFO:0005438", "immature conventional dendritic cell": "CL:0000840", "amnesia": "EFO:1001454", "marasmus": "EFO:1001033", "acrylamide": "CHEBI:28619", "LP1": "EFO:0003055", "low affinity immunoglobulin epsilon Fc receptor measurement": "EFO:0008210", "invasive ductal carcinoma": "EFO:0000186", "Hyperinsulinism due to INSR deficiency": "Orphanet:263458", "bile reflux": "EFO:1000838", "glutamatergic neuron": "CL:0000679", "Acute hepatic porphyria": "Orphanet:95157", "lactadherin measurement": "EFO:0008203", "Litomosoides sigmodontis": "NCBITaxon:42156", "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis": "Orphanet:88924", "Brachypodium distachyon": "NCBITaxon:15368", "Takotsubo cardiomyopathy": "EFO:1002000", "KYSE-450": "EFO:0006630", "late embryo": "UBERON:0000323", "Pure hair and nail ectodermal dysplasia": "Orphanet:69084", "central memory CD8 positive, alpha-beta T cell": "CL:0000907", "Caco-2": "EFO:0001099", "gliosarcoma": "EFO:1001465", "Pre-Descemet corneal dystrophy": "Orphanet:293462", "Myoviridae": "NCBITaxon:10662", "Kapur-Toriello syndrome": "Orphanet:2328", "Desminopathy": "Orphanet:98909", "Autosomal recessive Stickler syndrome": "Orphanet:250984", "Streptococcus pseudopneumoniae": "NCBITaxon:257758", "Gr1-high classical monocyte": "CL:0002395", "Tacaribe virus": "NCBITaxon:11631", "telencephalon": "UBERON:0001893", "primary neuron hindbrain": "ZFA:0000821", "S-adenosyl-L-methionine": "CHEBI:15414", "intracranial subdural hematoma": "EFO:1001801", "(1->3)-beta-D-glucan": "CHEBI:37671", "Hand-Arm Vibration Syndrome": "EFO:1001337", "genotype effect measurement": "EFO:0007958", "Soft Tissue Chondroma": "EFO:1000540", "Dentinogenesis imperfecta": "Orphanet:49042", "Disorder of purine or pyrimidine metabolism": "Orphanet:79224", "GM08390 {http": "CLO:0010523", "Oculotrichoanal syndrome": "Orphanet:2717", "Burkholderia thailandensis": "NCBITaxon:57975", "Histidinemia": "Orphanet:2157", "miTRAP": "EFO:0008818", "interleukin-4 (Homo sapiens)": "EFO:0003296", "insulin like growth factor measurement": "EFO:0004628", "CS57587": "EFO:0000024", "vitamin A deficiency": "EFO:1001237", "breast fibrocystic disease": "EFO:0003014", "cinnamaldehyde": "CHEBI:16731", "Ralstonia syzygii": "NCBITaxon:28097", "Genetic epidermal appendage anomaly": "Orphanet:183447", "cryptococcosis": "EFO:0007229", "Human adenovirus 4": "NCBITaxon:28280", "Autosomal recessive frontotemporal pachygyria": "Orphanet:329329", "muscle of head": "UBERON:0002376", "FRAXE intellectual disability": "Orphanet:100973", "Scarring alopecia of scalp {http": "HP:0004552", "drosophila developmental stage": "EFO:0005651", "GM15324 {http": "CLO:0027182", "juvenile days 30-44": "EFO:0001301", "translational bias design": "EFO:0001787", "PAC2": "EFO:0001224", "disease prognosis measurement": "EFO:0007936", "SHEP-2": "EFO:0005456", "complement C3 measurement": "EFO:0004983", "(-)-demecolcine": "CHEBI:4393", "cefuroxime": "CHEBI:3515", "KBG syndrome": "Orphanet:2332", "Leukocyte adhesion deficiency type III": "Orphanet:99844", "pharyngeal pouch 2": "UBERON:0007123", "19p13.13 microdeletion syndrome": "Orphanet:357001", "methionine S-oxide {http": "CHEBI:49033", "mercaptopurine": "CHEBI:50667", "Thymic Squamous Cell Carcinoma": "EFO:1000579", "AG04655 {http": "CLO:0034915", "hypercementosis": "EFO:1000970", "Hordeum vulgare subsp. vulgare": "NCBITaxon:112509", "antirheumatic drug": "CHEBI:35842", "Subdural Effusion": "EFO:1001429", "androsterone sulfate {http": "CHEBI:83037", "embryonic outer optic lobe primordium": "FBbt:00005822", "wine liking measurement": "EFO:0006949", "Cyprus facial-neuromusculoskeletal syndrome": "Orphanet:2674", "1-palmitoyl-2-palmitoleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:74000", "Theiler stage 26": "EFO:0002587", "Congenital vertical talus, unilateral": "Orphanet:295201", "nodular melanoma": "EFO:0008515", "Cohen syndrome": "Orphanet:193", "Salmonella enterica subsp. enterica serovar Pullorum": "NCBITaxon:605", "ML-DmD21": "EFO:0005829", "Wilson-Turner syndrome": "Orphanet:3459", "array scanning and feature extraction protocol": "EFO:0003814", "Autosomal dominant primary hypomagnesemia with hypocalciuria": "Orphanet:34528", "M\u00c3\u00bcllerian duct anomalies - limb anomalies": "Orphanet:2491", "Crotalus atrox": "NCBITaxon:8730", "antipsychotic drug use measurement": "EFO:0007792", "Hyper-IgM syndrome type 4": "Orphanet:101091", "lithium atom": "CHEBI:30145", "Pyruvate dehydrogenase E3-binding protein deficiency": "Orphanet:255182", "Severe intellectual disability - epilepsy - anal anomalies - distal phalangeal hypoplasia": "Orphanet:94066", "Ovarian Hyperandrogenism": "EFO:0009008", "Autosomal dominant methemoglobinemia": "Orphanet:330041", "Pilomatrixoma": "EFO:0009082", "hyperglobulinemic purpura": "EFO:1000972", "hip bone mineral density": "EFO:0007702", "septicemic plague": "EFO:0007481", "inferior colliculus": "UBERON:0001946", "clinical treatment": "EFO:0007056", "diffuse large B-cell lymphoma": "EFO:0000403", "polysorbate 20": "CHEBI:53424", "Eyebrow hypertrophy": "Orphanet:98596", "Familial omphalocele syndrome with facial dysmorphism": "Orphanet:280403", "Von Hippel anomaly": "Orphanet:98941", "schizoaffective disorder": "EFO:0005411", "scDNase-seq": "EFO:0008907", "Autosomal recessive limb-girdle muscular dystrophy type 2K": "Orphanet:86812", "acute hypotension": "EFO:0002497", "agranulocytosis": "HP:0012234", "Familial prostate cancer": "Orphanet:1331", "Syndromic agammaglobulinemia": "Orphanet:229720", "Acyrthosiphon pisum": "NCBITaxon:7029", "X-linked intellectual disability - psychosis - macroorchidism": "Orphanet:3077", "hepatitis B infection": "EFO:0004197", "thrombospondin-2 measurement": "EFO:0008299", "Tietz syndrome": "Orphanet:42665", "methyleugenol": "CHEBI:4918", "Bologna ecotype": "EFO:0005171", "AB1": "EFO:0004042", "Mast Cell Sarcoma": "EFO:1000364", "neuron projection": "GO:0043005", "rhombomere 4 floor plate": "UBERON:0005576", "recurrent infection": "HP:0002719", "intermediate uveitis": "EFO:1000986", "contactin-5 measurement": "EFO:0008101", "Familial flecked retinopathy": "Orphanet:227786", "Non-syndromic cerebral malformation due to abnormal neuronal migration": "Orphanet:163209", "ChIP-chip by array": "EFO:0002760", "postcranial axial skeleton": "UBERON:0002090", "oxygen saturation measurement": "EFO:0005682", "Partial deletion of the short arm of chromosome 1": "Orphanet:261857", "NCI-H889": "EFO:0006697", "sample pooling": "EFO:0005316", "49,XXXYY syndrome": "Orphanet:261534", "Pigmented palpebral tumor": "Orphanet:98586", "Hs 255.T": "EFO:0006584", "Alzheimers disease": "EFO:0000249", "Oscheius tipulae": "NCBITaxon:141969", "PK-45P": "EFO:0006735", "1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:75034", "Trichophyton longifusum": "NCBITaxon:446639", "Human herpesvirus 8": "NCBITaxon:37296", "Pithomyces chartarum": "NCBITaxon:1547544", "17q23.1q23.2 microdeletion syndrome": "Orphanet:261279", "femur": "UBERON:0000981", "interleukin (Homo sapiens)": "EFO:0003791", "67NR": "EFO:0002039", "Penaeus monodon": "NCBITaxon:6687", "acquired cold urticaria": "EFO:1001871", "AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome": "EFO:0009015", "Fibrous Hamartoma of Infancy": "EFO:1000257", "microgram per kilogram": "EFO:0002899", "plasma renin activity measurement": "EFO:0006828", "Silver-Russell syndrome": "Orphanet:813", "Metabolic disease with macular cherry-red spot": "Orphanet:98714", "Nestor-Guillermo progeria syndrome": "Orphanet:280576", "Abnormality of neuronal migration {http": "HP:0002269", "Physcomitrella patens": "NCBITaxon:3218", "tetracycline": "CHEBI:27902", "Brodmann (1909) area 46 {http": "UBERON:0006483", "Kyphomelic dysplasia": "Orphanet:1801", "colorectal adenocarcinoma": "EFO:0000365", "Syndactyly-polydactyly-ear lobe syndrome": "Orphanet:3259", "Follicular Variant Thyroid Gland Papillary Carcinoma": "EFO:1000261", "endothelin-1": "CHEBI:153671", "cytoplasmic vesicle membrane": "GO:0030659", "pneumococcal pneumonia": "EFO:1001474", "Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency": "Orphanet:314376", "hepatic vein thrombosis": "EFO:1000966", "cervical rib syndrome": "EFO:1000861", "Inherited congenital spastic tetraplegia": "Orphanet:210141", "fox fordyce disease": "EFO:1000703", "infant head circumference": "EFO:0004577", "ventricular tachycardia": "EFO:0005306", "cyclophosphamide": "CHEBI:4027", "serum iron measurement": "EFO:0006332", "morbid obesity": "EFO:0001074", "HITS-RAP": "EFO:0008766", "X-linked dominant intellectual disability - epilepsy": "Orphanet:93951", "Preaxial polydactyly of toes, unilateral": "Orphanet:295175", "Distal monosomy 15q": "Orphanet:1596", "Symbrachydactyly of hand and foot, bilateral": "Orphanet:295138", "terminal nerve": "UBERON:0002924", "curcumin": "CHEBI:3962", "Congenital glaucoma": "Orphanet:98976", "MDAMB175VII": "EFO:0001208", "Sterol metabolism disorder": "Orphanet:79226", "Partial duplication of the short arm of chromosome 6": "Orphanet:262740", "LNCAP": "EFO:0002071", "Maternal uniparental disomy of chromosome 20": "Orphanet:96186", "benserazide": "CHEBI:64187", "Familial syringomyelia": "Orphanet:370034", "Autosomal dominant progressive nephropathy with hypertension": "Orphanet:88659", "dsRNA-Seq": "EFO:0008726", "cholesteatoma of external ear": "EFO:1000677", "Mal de Meleda": "Orphanet:87503", "carpal tunnel syndrome": "EFO:0004143", "sertraline hydrochloride": "CHEBI:9124", "Fryns syndrome": "Orphanet:2059", "Difficulty walking {http": "HP:0002355", "mIMCD-3": "EFO:0002073", "Hereditary proximal myopathy with early respiratory failure": "Orphanet:178464", "LM-Seq": "EFO:0008786", "Trichophyton verrucosum": "NCBITaxon:63417", "Lethal restrictive dermopathy": "Orphanet:1662", "Distal myopathy with anterior tibial onset": "Orphanet:178400", "morphine": "CHEBI:17303", "plant fluid": "EFO:0000994", "L-ascorbic acid": "CHEBI:29073", "total iron binding capacity": "EFO:0006334", "lymphoid neoplasm": "EFO:0001642", "928 mel": "EFO:0006360", "wing disc": "UBERON:6001778", "Distal 7q11.23 microduplication syndrome": "Orphanet:261102", "renal artery obstruction": "EFO:1001150", "Abnormality of muscle physiology": "HP:0011804", "Syndrome with 46,XX disorder of sex development": "Orphanet:325109", "Be2 cell": "CL:0000944", "acute disseminated encephalomyelitis": "EFO:0007130", "ACHN": "EFO:0002108", "Francisella tularensis subsp. holarctica LVS": "NCBITaxon:376619", "Mucolipidosis": "Orphanet:79212", "Myofibrillar myopathy": "Orphanet:593", "Fusion-seq": "EFO:0008749", "mesothelial cell": "CL:0000077", "Lactobacillus brevis": "NCBITaxon:1580", "Familial clubfoot due to 17q23.1q23.2 microduplication": "Orphanet:238578", "X-linked intellectual disability, Brooks type": "Orphanet:3056", "pimozide": "CHEBI:8212", "Theiler stage 21": "EFO:0002584", "Limb-girdle muscular dystrophy": "Orphanet:263", "foot and mouth disease": "EFO:0007277", "Autosomal dominant proximal spinal muscular atrophy": "Orphanet:211037", "SPLAT": "EFO:0008946", "reflex sympathetic dystrophy": "EFO:1001147", "gastroenteritis": "EFO:1001463", "liver amyloid deposition measurement": "EFO:0008374", "small intestine": "UBERON:0002108", "Amborella trichopoda": "NCBITaxon:13333", "effector T cell": "CL:0000911", "primary Rickettsiaceae infectious disease": "EFO:1001128", "Nematostella vectensis": "NCBITaxon:45351", "nicotine glucuronidation measurement": "EFO:0006507", "ILSXISS122/TejJ": "EFO:0003011", "Mast Cell Neoplasm": "EFO:0009000", "Cloverleaf skull - asphyxiating thoracic dysplasia": "Orphanet:100978", "15q14 microdeletion syndrome": "Orphanet:261190", "SB 224289 hydrochloride": "CHEBI:64067", "multiple chemical sensitivity": "EFO:0007382", "pulmonary artery enlargement": "EFO:0006347", "Femoral bowing {http": "HP:0002980", "LOU-NH91": "EFO:0006638", "Eurotium amstelodami": "NCBITaxon:5054", "9q21 microdeletion syndrome": "Orphanet:352665", "cadmium compounds": "CHEBI:22978", "disease free survival": "EFO:0000409", "computed tomography": "EFO:0003960", "nucleolus": "GO:0005730", "ageusia": "EFO:1001758", "Spasticity-ataxia-gait anomalies syndrome": "Orphanet:401866", "Brachyolmia": "Orphanet:1293", "gonad {http": "UBERON:0000991", "Rosselli-Gulienetti syndrome": "Orphanet:90339", "picogram": "UO:0000025", "Qualitative or quantitative defects of troponin": "Orphanet:284786", "Paroxysmal exertion-induced dyskinesia": "Orphanet:98811", "Tibial muscular dystrophy": "Orphanet:609", "immature Vgamma2-positive thymocyte": "CL:0002406", "pemphigus": "EFO:1000749", "AG07139 {http": "CLO:0035608", "Granular Cell Tumor of the Neurohypophysis": "EFO:1000285", "Synovial Chondromatosis": "EFO:1000557", "pathogenicity": "IDO:0000450", "Thyroid hemiagenesis": "Orphanet:95719", "Rattus rattus": "NCBITaxon:10117", "sensory perception of smell": "GO:0007608", "prednisolone": "CHEBI:8378", "Ring chromosome 17": "Orphanet:1441", "Brachydactyly type B": "Orphanet:93383", "neck": "UBERON:0000974", "Tracheal anomaly": "Orphanet:156252", "Familial intestinal malrotation - facial anomalies": "Orphanet:2454", "Ulna hypoplasia - intellectual disability": "Orphanet:2249", "Sclerodermatomyositis": "EFO:1001995", "Bartonella koehlerae": "NCBITaxon:92181", "cup-to-disc ratio measurement": "EFO:0006939", "dermatologic drug": "CHEBI:50177", "cerebrospinal fluid biomarker measurement": "EFO:0006794", "Triose phosphate-isomerase deficiency": "Orphanet:868", "olfactory region": "UBERON:0003112", "Photobacterium profundum": "NCBITaxon:74109", "embryonic proventriculus inner layer": "FBbt:00005608", "xylem {http": "PO:0005352", "response to cold": "GO:0009409", "ChIPmentation": "EFO:0008686", "Woolly hair": "Orphanet:170", "oral submucous fibrosis": "EFO:1001818", "Danio rerio": "NCBITaxon:7955", "King-Denborough syndrome": "Orphanet:99741", "1-arachidonoyl-sn-glycero-3-phosphoethanolamine {http": "CHEBI:64395", "Genetic syndrome with a cerebellar malformation as major feature": "Orphanet:269567", "Congenital disorder of glycosylation": "Orphanet:137", "bacterial endocarditis": "EFO:1000830", "iPS DF 4.7": "EFO:0007097", "Herpes simplex infection": "EFO:1002022", "long lived plasma cell": "CL:0000974", "midbrain": "UBERON:0001891", "Dentocutaneous disease with cataract": "Orphanet:98649", "Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant": "EFO:1000303", "von Willebrand factor measurement": "EFO:0004629", "pronephros": "UBERON:0002120", "acquired metabolic disease": "EFO:1000639", "labelling": "EFO:0000562", "Qualitative or quantitative defects of protein O-mannosyltransferase 1": "Orphanet:209030", "Hypertelorism, Teebi type": "Orphanet:1519", "root endodermis {http": "PO:0005059", "ankylosing spondylitis": "EFO:0003898", "autoimmune thrombocytopenic purpura": "EFO:0007160", "KMS-28BM": "EFO:0006617", "16p11.2p12.2 microduplication syndrome": "Orphanet:261204", "Streptococcus pneumoniae D39": "NCBITaxon:373153", "KMS-12-PE": "EFO:0006613", "Intellectual disability-severe speech delay-mild dysmorphism syndrome": "Orphanet:391372", "dilated cardiomyopathy": "EFO:0000407", "Kaposi's sarcoma cell": "EFO:0000187", "Familial keratoacanthoma": "Orphanet:493", "Puccinia striiformis f. sp. tritici {http": "NCBITaxon:168172", "NKGA2-positive natural killer cell": "CL:0002439", "WSU-DLCL2": "EFO:0006775", "Partial deletion of the long arm of chromosome 22": "Orphanet:262182", "Qualitative or quantitative defects of perlecan": "Orphanet:207101", "stressful life event measurement": "EFO:0007781", "lymphatic system disease": "EFO:0007352", "LDL cholesterol": "EFO:0004195", "Robertsonian translocation": "EFO:0000393", "1,9-dideoxyforskolin": "CHEBI:50295", "Rare hemorrhagic disorder due to a constitutional coagulation factors defect": "Orphanet:68334", "Trematode Infections": "EFO:1001438", "Colon Juvenile Polyp": "EFO:1000185", "Autosomal dominant spastic paraplegia type 19": "Orphanet:100999", "plasma clusterin measurement": "EFO:0007656", "Periprosthetic Fractures": "EFO:1001823", "rhombomere 2": "UBERON:0005569", "tegmentum": "UBERON:0024151", "square meter": "UO:0000080", "HCC2911": "EFO:0006435", "periarthritis": "EFO:1001097", "Legionella pneumophila": "NCBITaxon:446", "paronychia": "EFO:0007421", "osteitis fibrosa": "EFO:0007413", "Lactobacillus kimchii": "NCBITaxon:103818", "Aspergillus flavus": "NCBITaxon:5059", "metagenomic data": "EFO:0004602", "Cervus nippon": "NCBITaxon:9863", "TYK-nu.CP-r": "EFO:0006767", "head mesoderm": "FBbt:00000127", "susceptibility to chickenpox measurement": "EFO:0008400", "neuroimaging measurement": "EFO:0004346", "lower body strength measurement": "EFO:0007999", "IgG galactosylation measurement": "EFO:0008425", "hyperprolactinemia": "EFO:0007319", "CS57591": "EFO:0000025", "2-palmitoyl-sn-glycero-3-phosphocholine {http": "CHEBI:76078", "Choreoacanthocytosis": "Orphanet:2388", "rectal prolapse": "HP:0002035", "interstitial dendritic cell": "CL:0001007", "retinal ganglion": "EFO:0002691", "Leigh syndrome with cardiomyopathy": "Orphanet:70474", "Bowen-Conradi syndrome": "Orphanet:1270", "ovarian follicle stage III": "UBERON:2001266", "Keratosis palmoplantaris striata": "Orphanet:50942", "cystoisosporiasis": "EFO:0007232", "sporophyte vegetative stage {http": "PO:0007134", "intuition": "EFO:0004334", "low molecular weight phosphotyrosine protein phosphatase measurement": "EFO:0008213", "cranial vasculature": "UBERON:0002200", "Duplication/inversion 15q11": "Orphanet:3306", "response to epirubicin": "GO:1902522", "Ptomaphagus": "NCBITaxon:351534", "Metabolic disease with corneal opacity": "Orphanet:98711", "Macroglossia": "Orphanet:156207", "vitamin B12 deficiency": "EFO:0000734", "cytoplasm": "GO:0005737", "Syndrome with 46,XY disorder of sex development": "Orphanet:98087", "peroneal nerve paralysis": "EFO:1001102", "embryonic central nervous system": "EFO:0000447", "Genetic neuro-ophthalmological disease": "Orphanet:183616", "Alpha-thalassemia - X-linked intellectual disability syndrome": "Orphanet:847", "Hepatic Granuloma": "EFO:1000291", "Kufor-Rakeb syndrome": "Orphanet:306674", "haemonchiasis": "EFO:0007293", "retinal detachment": "EFO:0005773", "Fraction B/C precursor B cell": "CL:0002400", "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy": "Orphanet:329336", "GM17174 {http": "CLO:0014034", "Antwerpen ecotype": "EFO:0006983", "Palpebral tumor": "Orphanet:98580", "coronary aneurysm": "EFO:1000881", "spermidine {http": "CHEBI:16610", "serum IgA measurement": "EFO:0004912", "HA-Flag protein fusion library": "EFO:0007568", "A375": "EFO:0002103", "ML-DmD23-c4": "EFO:0007114", "MHC-II-negative non-classical monocyte": "CL:0002471", "Nausea and vomiting": "HP:0002017", "Fish-eye disease": "Orphanet:79292", "Flavobacteriaceae Infections": "EFO:1001327", "Benign partial epilepsy with secondarily generalized seizures in infancy": "Orphanet:166302", "Citrullus lanatus": "NCBITaxon:3654", "Corneal dystrophy": "Orphanet:34533", "Atherosclerosis - deafness - diabetes - epilepsy - nephropathy": "Orphanet:1192", "Retropharyngeal Abscess": "EFO:1001415", "nucleated reticulocyte": "CL:0002421", "choriocarcinoma": "EFO:0002893", "purine-containing compound metabolic process": "GO:0072521", "EEC syndrome": "Orphanet:1896", "congenital generalized lipodystrophy": "EFO:1000681", "Clark level V": "EFO:0004961", "Brassica juncea": "NCBITaxon:3707", "Anguilla anguilla": "NCBITaxon:7936", "Jurkat": "EFO:0002796", "Autosomal dominant centronuclear myopathy": "Orphanet:169189", "Quartz-Seq": "EFO:0008877", "shoot apex {http": "PO:0000037", "matrix metalloproteinase 8 measurement": "EFO:0008466", "CX-1": "EFO:0006561", "pityriasis rosea": "EFO:1000756", "myopathy": "EFO:0004145", "cancer cell line": "EFO:0001639", "DOORS syndrome": "Orphanet:79500", "GM17257 {http": "CLO:0014393", "Mixed Tumor of the Skin": "EFO:1000385", "Osteoblastoma": "EFO:1000410", "ELR": "EFO:0007750", "mammary stem cell": "CL:0002451", "GM17736 {http": "CLO:0017043", "Mosaic variegated aneuploidy syndrome": "Orphanet:1052", "exome sequencing": "EFO:0005396", "apolipoprotein E isoform E2 measurement": "EFO:0008028", "lachrymal gland lesion": "EFO:0007125", "phenylacetate {http": "CHEBI:18401", "Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies": "Orphanet:352687", "GM15216 {http": "CLO:0027491", "glyburide": "CHEBI:5441", "white-sutton syndrome": "EFO:0009079", "Neurologic Waardenburg-Shah syndrome": "Orphanet:163746", "fluroanthene": "CHEBI:33083", "ascending colon": "UBERON:0001156", "radiation-induced gastrointestinal mucositis": "EFO:1001914", "BICR 78": "EFO:0006543", "EPIG-Seq": "EFO:0008731", "bone development disease": "EFO:0005541", "Focal facial dermal dysplasia type II": "Orphanet:398173", "chronic fatigue syndrome": "EFO:0004540", "CGR8": "EFO:0006273", "Oculoauricular syndrome, Schorderet type": "Orphanet:157962", "RCM-1": "EFO:0006476", "Arthroderma benhamiae": "NCBITaxon:63400", "anorexia nervosa": "EFO:0004215", "CD4-positive CD11b-positive dendritic cell": "CL:0000999", "CL-11": "EFO:0006368", "GM06999": "EFO:0007077", "Adult-onset autosomal recessive cerebellar ataxia": "Orphanet:284289", "sign or symptom": "EFO:0003765", "amitriptyline": "CHEBI:2666", "cobalt dichloride": "CHEBI:35696", "Oculocerebral hypopigmentation syndrome, Cross type": "Orphanet:2719", "CS57828": "EFO:0000136", "Hs 940.T": "EFO:0006595", "interleukin-13 (Mus musculus)": "EFO:0003798", "COLO 857": "EFO:0006381", "total trans-18": "EFO:0006823", "Butterfly-shaped pigment dystrophy": "Orphanet:99001", "saliva-secreting gland": "UBERON:0001044", "Autosomal recessive limb-girdle muscular dystrophy type 2Q": "Orphanet:254361", "Autosomal dominant omodysplasia": "Orphanet:93328", "social desirability": "EFO:0004366", "fluphenazine": "CHEBI:5123", "palmitoleate {http": "CHEBI:32372", "Dysspondyloenchondromatosis": "Orphanet:85198", "NCI-H1355": "EFO:0002251", "Ly49D-negative natural killer cell": "CL:0002445", "Nevus of Ito": "EFO:1000395", "premature menopause": "EFO:0009005", "biliary tract neoplasm": "EFO:0003891", "Hereditary poikiloderma": "Orphanet:222628", "TCC-PAN2": "EFO:0006764", "Lethal congenital contracture syndrome type 3": "Orphanet:137783", "tuberculous peritonitis": "EFO:0007529", "arthropod fat body {http": "UBERON:0003917", "Generalized epilepsy with febrile seizures-plus": "Orphanet:36387", "MITF-related melanoma and renal cell carcinoma predisposition syndrome": "Orphanet:293822", "taurodeoxycholate {http": "CHEBI:36261", "Deafness - ear malformation - facial palsy": "Orphanet:3232", "stomatal complex": "PO:0002000", "SW684": "EFO:0002369", "colorectal cancer cell": "BTO:0001615", "carotid artery external diameter measurement": "EFO:0007719", "Encephalopathy {http": "HP:0001298", "Corticosteroid-binding globulin deficiency": "Orphanet:199247", "sarcopenia": "EFO:1000653", "marginal blastomere": "ZFA:0000541", "gastrointestinal system": "UBERON:0005409", "atorvastatin": "CHEBI:39548", "Marfanoid habitus - intellectual disability, autosomal recessive": "Orphanet:2463", "Ichthyosis - alopecia - eclabion - ectropion - intellectual disability": "Orphanet:2269", "HCC2157": "EFO:0001177", "pathological process": "OBI:1110122", "mucormycosis": "EFO:0007380", "masseter muscle": "UBERON:0001597", "placenta praevia": "EFO:0007442", "Pyrococcus furiosus DSM 3638": "NCBITaxon:186497", "MC116": "EFO:0002228", "gene methylation measurement": "EFO:0006959", "pressure unit": "UO:0000109", "jasmonic acids": "CHEBI:24937", "BY5251": "EFO:0000100", "nodular goiter": "EFO:1001062", "Streptomyces exfoliatus": "NCBITaxon:1905", "VirScan": "EFO:0008983", "CD8-positive, alpha-beta memory T cell": "CL:0000909", "Acidithiobacillus ferrooxidans ATCC 23270": "NCBITaxon:243159", "Zingiber officinale": "NCBITaxon:94328", "hippocampus CA2": "UBERON:0003882", "Oryza nivara": "NCBITaxon:4536", "HCC0033": "EFO:0006417", "Bacteroides thetaiotaomicron": "NCBITaxon:818", "RT4-D6P2T cell": "BTO:0001205", "trigeminal ganglion": "UBERON:0001675", "Burkholderia pseudomallei": "NCBITaxon:28450", "Vgamma1.1-positive, Vdelta6.3-negative thymocyte": "CL:0002411", "Dopa-responsive dystonia due to sepiapterin reductase deficiency": "Orphanet:70594", "manganese poisoning": "EFO:1001808", "Achondroplasia": "Orphanet:15", "Teleopsis dalmanni": "NCBITaxon:139649", "Thymic-renal-anal-lung dysplasia": "Orphanet:3326", "ANE syndrome": "Orphanet:157954", "respiratory system": "UBERON:0001004", "CD103-positive, langerin-positive lymph node dendritic cell": "CL:0002509", "Human respiratory syncytial virus B1": "NCBITaxon:79692", "Congenital elbow dislocation, bilateral": "Orphanet:295227", "LP.19 nineteen leaves visible stage": "PO:0007120", "Trisomy 18": "Orphanet:3380", "Ablepharon macrostomia syndrome": "Orphanet:920", "Peters anomaly": "Orphanet:708", "C4-2B": "EFO:0006365", "ring gland": "UBERON:6001722", "T-lymphocyte surface antigen Ly-9 measurement": "EFO:0008295", "carotid artery measurement": "EFO:0007716", "Sezary's disease": "EFO:1000785", "hyperamylasemia": "EFO:1000969", "Beta-propeller protein-associated neurodegeneration": "Orphanet:329284", "Staphylococcus aureus carrier status": "EFO:0007756", "Choroideremia - hypopituitarism": "Orphanet:1434", "adrenal gland disease": "EFO:0005539", "Lamellar ichthyosis": "Orphanet:313", "wortmannin": "CHEBI:52289", "Illumina iSeq 100": "EFO:0008635", "Salix viminalis": "NCBITaxon:40686", "Paramecium tetraurelia": "NCBITaxon:5888", "biceps brachii": "UBERON:0001507", "Postaxial polydactyly type A, unilateral": "Orphanet:295163", "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency": "Orphanet:99898", "mosaic loss of chromosome Y measurement": "EFO:0007783", "wing": "UBERON:0000023", "Paternal 14q32.2 hypomethylation syndrome": "Orphanet:254531", "response to mepolizumab": "EFO:0008459", "Hepatic fibrosis": "HP:0001395", "taurine {http": "CHEBI:15891", "probe design element": "EFO:0004903", "Epinephelus coioides": "NCBITaxon:94232", "FASTQ format": "EFO:0004155", "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2": "Orphanet:177904", "X-linked intellectual disability, Kroes type": "Orphanet:163961", "Herpes Labialis": "EFO:1001347", "Wassilewskija ecotype": "EFO:0005156", "suntan": "EFO:0004279", "neurexophilin-1 measurement": "EFO:0008244", "Severe hemophilia B": "Orphanet:169793", "measles": "EFO:1002025", "Autosomal recessive limb-girdle muscular dystrophy type 2E": "Orphanet:119", "Thyroid Gland Diffuse Large B-Cell Lymphoma": "EFO:1000587", "giardiasis": "DOID:10718", "Salmonella enterica subsp. enterica serovar Typhi str. Ty2": "NCBITaxon:209261", "aseptic meningitis": "EFO:1000823", "serum creatinine measurement": "EFO:0004518", "Lower limb Muscle weakness {http": "HP:0007340", "Polysyndactyly, bilateral": "Orphanet:295161", "Femoral agenesis/hypoplasia": "Orphanet:1987", "MCCAR": "EFO:0002229", "Hermansky-Pudlak syndrome type 9": "Orphanet:280663", "ENCODE cell line": "EFO:0002926", "FREQ-Seq": "EFO:0008746", "Vitamin D": "CHEBI:27300", "cortical opacity measurement": "EFO:0005608", "Ocular albinism with congenital sensorineural deafness": "Orphanet:352740", "hypochlorous acid": "CHEBI:24757", "Solitary median maxillary central incisor syndrome": "Orphanet:2286", "Kallmann syndrome - heart disease": "Orphanet:2326", "cells per milliliter": "UO:0000201", "Parathyroid Hyperplasia": "EFO:1000457", "Disorder of branched-chain amino acid metabolism": "Orphanet:79197", "CBA/J": "EFO:0007735", "heart amyloid deposition measurement": "EFO:0008365", "Watermelon mosaic virus": "NCBITaxon:146500", "Epidermolytic palmoplantar keratoderma": "Orphanet:2199", "R28": "EFO:0001227", "Anaplastic (Malignant) Meningioma": "EFO:1000082", "interopercle": "UBERON:2000674", "transcription profiling by high throughput sequencing": "EFO:0002770", "Arthrogryposis due to muscular dystrophy": "Orphanet:1155", "Laron syndrome with immunodeficiency": "Orphanet:220465", "Mitochondrial DNA depletion syndrome": "Orphanet:35698", "Ring chromosome 20": "Orphanet:1444", "esophageal diverticulosis": "EFO:1000930", "olanzapine": "CHEBI:7735", "attomole": "UO:0000044", "anterior lateral line ganglion": "UBERON:2001391", "C-reactive protein measurement": "EFO:0004458", "Burkholderia mallei": "NCBITaxon:13373", "Kleefstra syndrome due to 9q34 microdeletion": "Orphanet:96147", "cis-Golgi network": "GO:0005801", "angiosarcoma": "EFO:0003968", "nucleobase-containing compound biosynthetic process": "GO:0034654", "Hereditary isolated aplastic anemia": "Orphanet:397692", "Theiler stage 25": "EFO:0004412", "Pseudomonas fluorescens Pf-5": "NCBITaxon:220664", "sulmazole": "CHEBI:34988", "gustatory system": "UBERON:0001033", "Pyridoxal phosphate-responsive seizures": "Orphanet:79096", "RPMI 2650": "EFO:0006478", "coated vesicle membrane": "GO:0030662", "Ichthyophthirius multifiliis": "NCBITaxon:5932", "Craniosynostosis - anal anomalies - porokeratosis": "Orphanet:85199", "Monoamine oxidase A deficiency": "Orphanet:3057", "Obesity due to MC3R deficiency": "Orphanet:217031", "histiocytic medullary reticulosis": "EFO:1001499", "GM17752 {http": "CLO:0016561", "N-acetylputrescine {http": "CHEBI:17768", "pathological myopia": "EFO:0004207", "chlorphenamine": "CHEBI:52010", "Achondrogenesis type 2": "Orphanet:93296", "hepatic tuberculosis": "EFO:0007302", "Ly49CI-negative natural killer cell": "CL:0002446", "Synostosis - microcephaly - scoliosis": "Orphanet:3268", "CLN6 disease": "Orphanet:228363", "Ex-FISH": "EFO:0008993", "alpha-2-macroglobulin receptor-associated protein measurement": "EFO:0008021", "behavior": "GO:0007610", "Burkholderia ambifaria": "NCBITaxon:152480", "Malignant Pleural Neoplasm": "EFO:1000362", "PFSK-1": "EFO:0005234", "Benign familial nocturnal alternating hemiplegia of childhood": "Orphanet:209973", "Partington syndrome": "Orphanet:94083", "ventilator-associated pneumonia": "EFO:1001865", "CYP3A4 activity": "EFO:0004910", "Hypocalcemic rickets": "Orphanet:289103", "Familial multinodular goiter": "Orphanet:276399", "Dysostosis, Stanescu type": "Orphanet:1798", "Penicillium italicum": "NCBITaxon:40296", "central brain anlage": "FBbt:00015256", "X-linked Charcot-Marie-Tooth disease": "Orphanet:64747", "Kin-S49": "EFO:0001197", "abnormal glucose tolerance": "EFO:0002546", "1,2-di-[(9Z,12Z)-octadecadienoyl]-sn-glycero-3-phosphocholine {http": "CHEBI:42027", "Partial deletion of the short arm of chromosome 4": "Orphanet:261884", "Endarteritis": "EFO:0009084", "adenomyoma": "EFO:0007133", "NCI-H2347": "EFO:0002287", "Cytomegalovirus Retinitis": "EFO:1001302", "cancerophobia": "EFO:1001879", "coleoptile emergence stage": "PO:0007045", "Hypertrichosis-acromegaloid facial appearance syndrome": "Orphanet:966", "GAPO syndrome": "Orphanet:2067", "rhombomere 6 floor plate": "UBERON:0005582", "ES-E14TG2a.4": "EFO:0007751", "Niemann-Pick disease type B": "Orphanet:77293", "oseltamivir": "CHEBI:7798", "pineal complex": "UBERON:0015238", "methoxychlor": "CHEBI:6842", "microgram per gram body weight": "EFO:0007055", "Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency": "Orphanet:284435", "Thyroid ectopia": "Orphanet:95712", "corneal epithelium": "UBERON:0001772", "Autosomal dominant distal myopathy": "Orphanet:206650", "Epibulbar lipodermoid - preauricular appendage - polythelia": "Orphanet:231742", "exocrine pancreas cell": "CL:0000083", "Skin ulcer": "HP:0200042", "intermittent vascular claudication": "EFO:0003876", "Hereditary sclerosing poikiloderma with tendon and pulmonary involvement": "Orphanet:221043", "FRISCR": "EFO:0008747", "Sitosterolemia": "Orphanet:2882", "CB4858": "EFO:0004093", "dendritic cell-derived intermediate cell": "EFO:0002661", "adhesion factor": "EFO:0004521", "Abnormality of the respiratory system": "HP:0002086", "Segmental progressive overgrowth syndrome with fibroadipose hyperplasia": "Orphanet:314662", "Transcobalamin deficiency": "Orphanet:859", "EM464": "EFO:0004066", "Bencze syndrome": "Orphanet:1241", "Isolated amyelia": "Orphanet:268868", "cold temperature regimen": "EO:0007174", "Aniridia": "Orphanet:77", "LHSR": "EFO:0002797", "Familial multiple fibrofolliculoma": "Orphanet:338", "ethyl glucuronide {http": "CHEBI:87248", "genomic data": "EFO:0004600", "Anemia due to adenosine triphosphatase deficiency": "Orphanet:1044", "myoglobin measurement": "EFO:0005057", "mature CD4 single-positive thymocyte": "CL:0002436", "heart tube": "UBERON:0004141", "Pseudohypoaldosteronism type 1": "Orphanet:756", "Droplet-CirSeq": "EFO:0008723", "fertilized ovule stage {http": "PO:0004505", "Pyle disease": "Orphanet:3005", "Disease with focal palmoplantar keratoderma as a major feature": "Orphanet:307871", "Niemann-Pick disease type C, adult neurologic onset": "Orphanet:216986", "Deltaretrovirus Infections": "EFO:1001303", "SSR4-CDG": "Orphanet:370927", "Autosomal recessive spastic paraplegia type 76": "EFO:0009019", "Blepharophimosis - epicanthus inversus - ptosis due to polyA expansion": "Orphanet:261579", "GM17227 {http": "CLO:0014358", "RIP-seq": "EFO:0005310", "129X1/SvJ": "EFO:0000600", "anal gland neoplasm": "EFO:1000804", "Inclusion Body Fibromatosis": "EFO:1000301", "Microcephaly - cardiac defect - lung malsegmentation": "Orphanet:2516", "latent syphilis": "EFO:0007340", "Hypopigmentation-punctate palmoplantar keratoderma syndrome": "Orphanet:324561", "GMUCT 1.0": "EFO:0008752", "dorsal ectoderm primordium": "EFO:0000416", "orbit": "BTO:0004687", "Posterior corneal dystrophy": "Orphanet:98627", "nail": "UBERON:0001705", "mast cell": "CL:0000097", "heterocycle metabolic process": "GO:0046483", "Cystic fibrosis": "Orphanet:586", "Stormorken-Sjaastad-Langslet syndrome": "Orphanet:3204", "Spinal atrophy - ophthalmoplegia - pyramidal syndrome": "Orphanet:1217", "EnIGMA": "EFO:0008730", "losartan": "CHEBI:6541", "Adult-onset nemaline myopathy": "Orphanet:171442", "clinical ideal cardiovascular health": "EFO:0007653", "CD117-positive common myeloid progenitor OR CD217-positive common lymphoid progenitor": "CL:0001030", "ocular cicatricial pemphigoid": "EFO:0008610", "chromatid break measurement": "EFO:0007593", "Crimean-Congo hemorrhagic fever virus": "NCBITaxon:11593", "AB SOLiD System": "EFO:0004435", "Helicobacter pylori J99": "NCBITaxon:85963", "Laryngeal Adenoid Cystic Carcinoma": "EFO:1000319", "plant growth hormone": "CHEBI:37848", "Bardet-Biedl syndrome 5": "EFO:0009025", "vaginal inflammation": "EFO:0005757", "Adult-onset autosomal recessive sideroblastic anemia": "Orphanet:255132", "McDonough syndrome": "Orphanet:2471", "array reporter": "EFO:0005072", "rhombomere": "UBERON:0001892", "response to ximelagatran": "GO:0036288", "Syndactyly type 4": "Orphanet:93405", "Congenital muscular dystrophy with intellectual disability and severe epilepsy": "Orphanet:329178", "GM17118 {http": "CLO:0014951", "floral transition": "EFO:0002683", "tenascin measurement": "EFO:0008296", "HapMap cell line": "EFO:0002933", "Osteocraniostenosis": "Orphanet:2763", "methyl glyoxal": "CHEBI:17158", "C3H10T1/2": "EFO:0002816", "single cell nucleic acid sequencing protocol": "EFO:0008439", "4-fluoro-N-\\\\\\{2-[4-(7-methoxynaphthalen-1-yl)piperazin-1-yl]ethyl\\\\\\}benzamide hydrochloride": "CHEBI:64099", "Filoviridae infectious disease": "EFO:0007273", "GM14433 {http": "CLO:0031236", "hypertrophy": "EFO:0002460", "Primary bone dysplasia with increased bone density": "Orphanet:93444", "milliliter": "UO:0000098", "Multiple mitochondrial DNA deletion syndrome": "Orphanet:254807", "Male infertility with spermatogenesis disorder": "Orphanet:399775", "AIDS-Related Primary Central Nervous System Lymphoma": "EFO:1000077", "ProP-PD": "EFO:0008871", "Lipoic acid synthetase deficiency": "Orphanet:401859", "S2R+": "EFO:0005837", "Congenital fibrosis of extraocular muscles": "Orphanet:45358", "Synaptic congenital myasthenic syndromes": "Orphanet:98915", "mexiletine": "CHEBI:6916", "valvula cerebelli": "UBERON:2000603", "peritoneal cavity {http": "UBERON:0001179", "Genetic dementia": "Orphanet:158124", "CD11b-positive dendritic cell": "CL:0002465", "Austrofundulus limnaeus": "NCBITaxon:52670", "Nephronophthisis": "Orphanet:655", "Mycobacterium avium complex disease": "EFO:0007386", "mosquito bite reaction itch intensity measurement": "EFO:0008377", "vesicle membrane": "GO:0012506", "inflorescence emergence stage": "PO:0007041", "gastrointestinal tract (lamina propria) macrophage": "CL:0000865", "Ovarian Gynandroblastoma": "EFO:1000422", "hFib2-iPS4": "EFO:0007951", "X-linked intellectual disability, Najm type": "Orphanet:163937", "CADO ES1": "EFO:0002818", "cofactor transport": "GO:0051181", "antisocial behaviour measurement": "EFO:0007052", "growth delay": "HP:0001510", "Metachromatic leukodystrophy, adult form": "Orphanet:309271", "Generalized juvenile polyposis/juvenile polyposis coli": "Orphanet:329971", "Richards-Rundle syndrome": "Orphanet:1399", "Congenital lipoid adrenal hyperplasia due to STAR deficency": "Orphanet:90790", "1-aminocyclopropane-1-carboxylic acid": "CHEBI:18053", "C-X-C motif chemokine 6 measurement": "EFO:0008059", "Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome": "Orphanet:363686", "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency": "Orphanet:319535", "Crohn's colitis": "EFO:0005622", "O-octanoyl-L-carnitine {http": "CHEBI:18102", "embryonic stage 1": "EFO:0005860", "gamma-tocopherol": "CHEBI:18185", "squamous cell lung carcinoma": "EFO:0000708", "urine": "UBERON:0001088", "2-\\\\\\{[(2E)-3-iodoprop-2-en-1-yl](propyl)amino\\\\\\}tetralin-7-ol maleate": "CHEBI:64134", "vitreous prolapse": "EFO:0008625", "intestinal perforation": "EFO:1000987", "Cholestasis-lymphedema syndrome": "Orphanet:1414", "Autosomal dominant vitreoretinochoroidopathy": "Orphanet:3086", "YEPG": "EFO:0007026", "TMD8": "EFO:0006496", "mitral valve": "UBERON:0002135", "Oblique facial cleft": "Orphanet:141253", "impetigo": "EFO:1000714", "elbow": "UBERON:0001461", "Juvenile primary lateral sclerosis": "Orphanet:247604", "Infantile glycine encephalopathy": "Orphanet:289860", "X-linked intellectual disability - acromegaly - hyperactivity": "Orphanet:85327", "Paired VH": "EFO:0008842", "Poikiloderma with neutropenia": "Orphanet:221046", "Benign infantile seizures associated to mild gastroenteritis": "Orphanet:166305", "cervix erosion": "EFO:1000862", "Adult-onset proximal spinal muscular atrophy, autosomal dominant": "Orphanet:209335", "GM14476 {http": "CLO:0031274", "Leptospira interrogans serovar Lai str. 56601": "NCBITaxon:189518", "whole chromosome random sequencing": "EFO:0004160", "inversion": "EFO:0004017", "Congenital intrauterine infection-like syndrome": "Orphanet:1229", "idiopathic pulmonary fibrosis": "EFO:0000768", "19q13.11 microdeletion syndrome": "Orphanet:217346", "Holocarboxylase synthetase deficiency": "Orphanet:79242", "susceptibility to chronic sinus infection measurement": "EFO:0008419", "Glomus intraradices": "NCBITaxon:4876", "Pulmonary alveolar microlithiasis": "Orphanet:60025", "border follicle cell": "CL:0000579", "3-fold embryo Ce": "EFO:0005499", "X-linked intellectual disability - macrocephaly - macroorchidism": "Orphanet:85320", "crown root {http": "PO:0000043", "Gastric Neuroendocrine Tumor G1": "EFO:1000275", "ILSXISS22/TejJ": "EFO:0002978", "1,4-dithiothreitol": "CHEBI:18320", "Microlissencephaly type B": "Orphanet:101052", "ileocolitis": "EFO:0005624", "bronchioloalveolar carcinoma": "EFO:1001941", "Atrichia with papular lesions": "Orphanet:86819", "CLN11 disease": "Orphanet:314629", "Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder": "Orphanet:98396", "lymphangitis": "EFO:0007351", "human Chorionic Gonadotropin measurement": "EFO:0008156", "Methicillin-Susceptible Staphylococcus Aureus Infection": "EFO:0008557", "cellular adhesion molecule measurement": "EFO:0008353", "Beckwith-Wiedemann syndrome due to 11p15 microduplication": "Orphanet:96076", "stem node {http": "PO:0020141", "MHH-ES-1": "EFO:0006650", "Familial multiple nevi flammei": "Orphanet:624", "IRVAN syndrome": "Orphanet:209943", "Hohenlieth ecotype": "EFO:0006964", "restrictive cardiomyopathy": "EFO:0002630", "puberty": "EFO:0001382", "response to thiopurine": "EFO:0006317", "GM17164 {http": "CLO:0013994", "AIDS phobia": "EFO:1001873", "GM17248 {http": "CLO:0014408", "clear cell adenocarcinoma": "EFO:0000348", "dopaminergic neuroblastoma": "EFO:0006391", "interleukin-33 (Rattus norvegicus)": "EFO:0003807", "Lipoatrophy": "HP:0100578", "TE85": "EFO:0002866", "SPET-seq": "EFO:0008945", "Hypotonia - failure to thrive - microcephaly": "Orphanet:79507", "regulation of ovulation": "GO:0060278", "wood parenchyma": "PO:0004532", "Atrophoderma vermiculata": "Orphanet:79100", "MAINE-Seq": "EFO:0008792", "BM1604": "EFO:0002117", "Cystinuria type B": "Orphanet:93613", "Malignant hyperthermia": "Orphanet:423", "Hereditary motor and sensory neuropathy type 6": "Orphanet:90120", "Congenital secondary polycythemia": "Orphanet:238536", "Dysplasia of Larynx": "EFO:1000227", "colonic mucosa": "UBERON:0000317", "Moderately severe hemophilia A": "Orphanet:169805", "NCI-H2135": "EFO:0006674", "Vogt-Koyanagi-Harada disease": "Orphanet:3437", "Macrostomia - preauricular tags - external ophthalmoplegia": "Orphanet:83619", "CS57810": "EFO:0000124", "gastric adenocarcinoma": "EFO:0000503", "dysuria": "EFO:0003901", "Disorder of neutral amino acid transport": "Orphanet:308451", "tibia": "UBERON:0000979", "Frontotemporal dementia": "Orphanet:282", "Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency": "Orphanet:284426", "posterior uveitis": "EFO:1001119", "Multiple endocrine neoplasia type 4": "Orphanet:276152", "atrial conduction disease": "EFO:0005304", "Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type": "Orphanet:394529", "muscle cell": "CL:0000187", "Frag-seq": "EFO:0008745", "Neofusicoccum parvum {http": "NCBITaxon:310453", "Genetic photodermatosis": "Orphanet:183490", "RNA assay": "EFO:0001457", "Otitis media": "EFO:0004992", "gastric bypass": "EFO:0005244", "White platelet syndrome": "Orphanet:370131", "Pontocerebellar hypoplasia type 2": "Orphanet:2524", "HEY": "EFO:0006580", "Trypanosoma cruzi": "NCBITaxon:5693", "scWGBS": "EFO:0008916", "Common variable immunodeficiency": "Orphanet:1572", "secretion by cell": "GO:0032940", "aortic valve prolapse": "EFO:1000815", "primary motor cortex": "UBERON:0001384", "hearing measurement": "EFO:0007616", "AG04450": "EFO:0006270", "Fanconi anemia complementation group F": "EFO:0009045", "Testicular Teratoma": "EFO:1000573", "digestive system disease": "EFO:0000405", "systolic blood pressure": "EFO:0006335", "multiple system atrophy": "EFO:1001050", "diffuse gastric adenocarcinoma": "EFO:0000402", "HUES9": "EFO:0007094", "aspergillosis": "EFO:0007157", "Dengue virus 2": "NCBITaxon:11060", "Madelung deformity, bilateral": "Orphanet:295223", "MEL-HO": "EFO:0006647", "Progeroid syndrome, Petty type": "Orphanet:2963", "optic primordium": "UBERON:0003071", "aortic disease": "EFO:0005775", "uncultured microorganism": "NCBITaxon:358574", "CD4": "EFO:0004839", "Genetic skin tumor": "Orphanet:183487", "response to TNF antagonist": "EFO:0004653", "U-87 MG": "EFO:0005237", "KLE": "EFO:0002220", "Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure": "Orphanet:168609", "endemic goiter": "EFO:1000916", "Classic Bartter syndrome": "Orphanet:93605", "HDMYZ": "EFO:0002190", "JinB8": "EFO:0006281", "Heart-hand syndrome type 2": "Orphanet:1350", "Carpenter syndrome": "Orphanet:65759", "Short rib-polydactyly syndrome, Saldino-Noonan type": "Orphanet:93270", "meibomian cyst": "EFO:0007363", "Myalgia": "HP:0003326", "Lethal Kniest-like dysplasia": "Orphanet:2347", "CD27-positive gamma-delta T cell": "CL:0002124", "response to trauma exposure": "EFO:0008483", "Salmonella enterica subsp. enterica serovar Muenster": "NCBITaxon:82689", "response to lithium ion": "GO:0010226", "Progressive familial intrahepatic cholestasis type 1": "Orphanet:79306", "mitotic spindle organization": "GO:0007052", "chenodeoxycholate {http": "CHEBI:36234", "Paralytic facial malformation": "Orphanet:156224", "head and neck disorder": "EFO:0000524", "specific phobia": "EFO:1001918", "ML-DmD4-c1": "EFO:0005831", "1q44 microdeletion syndrome": "Orphanet:238769", "Dystrophic epidermolysis bullosa pruriginosa": "Orphanet:89843", "response to terbinafine": "EFO:0007923", "Clark level": "EFO:0004956", "rheumatoid arthritis": "EFO:0000685", "Distal monosomy 19p13.3": "Orphanet:96129", "MOMO syndrome": "Orphanet:2563", "Ovis aries": "NCBITaxon:9940", "embryonic day 10.5": "EFO:0007643", "Progressive epilepsy and/or ataxia with myoclonus as a major feature": "Orphanet:306762", "Dorfman-Chanarin disease": "Orphanet:98907", "Rickettsia prowazekii": "NCBITaxon:782", "insomnia measurement": "EFO:0007876", "Lhermitte-Duclos disease": "Orphanet:65285", "Oncorhynchus gorbuscha": "NCBITaxon:8017", "Alzheimer's disease neuropathologic change": "EFO:0006801", "Genetic hyperaldosteronism": "Orphanet:371861", "Q fever": "EFO:0005224", "tryptophan": "CHEBI:27897", "cellular component": "GO:0005575", "Hi-C": "EFO:0007693", "Dirofilaria immitis": "NCBITaxon:6287", "Amelia of lower limb, unilateral": "Orphanet:295057", "12q14 microdeletion syndrome": "Orphanet:94063", "Polydactyly of a triphalangeal thumb, bilateral": "Orphanet:295150", "Microcystic corneal dystrophy": "Orphanet:98956", "primary root apical meristem": "PO:0006081", "Polysphondylium pallidum": "NCBITaxon:13642", "CS57776": "EFO:0000113", "Hyalitis": "EFO:0008628", "VC199": "EFO:0004092", "hematopoietic oligopotent progenitor cell": "CL:0002032", "zebrafish embryonic structure": "EFO:0003332", "Autosomal dominant limb-girdle muscular dystrophy type 1E": "Orphanet:34517", "KYSE30": "EFO:0002223", "central gray substance of midbrain {http": "UBERON:0003040", "GM17142 {http": "CLO:0013938", "sialic acid-binding Ig-like lectin 6 measurement": "EFO:0008285", "Congenital absence/hypoplasia of thumb, bilateral": "Orphanet:295112", "GM17249 {http": "CLO:0014409", "Tarlov Cysts": "EFO:1001858", "Central bilateral macrogyria": "Orphanet:2431", "GM17138 {http": "CLO:0015097", "Muscular pseudohypertrophy - hypothyroidism": "Orphanet:2349", "Brill-Zinsser disease": "EFO:0007182", "2-methylbutyrylcarnitine {http": "CHEBI:73026", "dicer1 syndrome": "EFO:0009068", "Kindalville ecotype": "EFO:0006966", "Combined immunodeficiency with skin granulomas": "Orphanet:157949", "Craniofacial dyssynostosis": "Orphanet:1516", "Primary central nervous system vasculitis": "Orphanet:140989", "SPARC-like protein 1 measurement": "EFO:0008289", "prohemocyte (sensu Nematoda and Protostomia)": "CL:0000385", "Schilbach-Rott syndrome": "Orphanet:2353", "C-C motif chemokine 25 measurement": "EFO:0008050", "external carotid artery": "UBERON:0001070", "calpastatin measurement": "EFO:0008065", "1-myristoyl-sn-glycero-3-phosphocholine {http": "CHEBI:64489", "normal pressure hydrocephalus": "EFO:1001065", "phosphorus": "CHEBI:28659", "coxsackievirus infectious disease": "EFO:0007226", "3',5'-cyclic AMP(1-) {http": "CHEBI:58165", "EAhy 926 cell": "EFO:0003039", "Congenital sialidosis type 2": "Orphanet:93400", "GM17139 {http": "CLO:0015098", "organic heterocyclic compound": "CHEBI:24532", "transforming growth factor-beta-induced protein ig-h3 measurement": "EFO:0008302", "hippocampal sclerosis of aging": "EFO:0005678", "Symptomatic form of Coffin-Lowry syndrome in female carriers": "Orphanet:276630", "BMI-adjusted hip bone size": "EFO:0008038", "gastric tubular adenocarcinoma": "EFO:1000030", "Streptococcus mutans": "NCBITaxon:1309", "Abnormality of the ear": "HP:0000598", "Fascioliasis": "EFO:1001324", "Spondyloepimetaphyseal dysplasia, Isidor type": "Orphanet:370015", "Malonic aciduria": "Orphanet:943", "Osteogenesis imperfecta - retinopathy - seizures - intellectual disability": "Orphanet:2773", "spiramide": "CHEBI:64207", "heart left ventricle": "UBERON:0002084", "Schizosaccharomyces pombe": "NCBITaxon:4896", "GM17814 {http": "CLO:0016508", "Paroxysmal dystonia": "Orphanet:200037", "milligram per milliliter": "UO:0000176", "gastroparesis": "EFO:1000948", "Partial duplication of the short arm of chromosome 17": "Orphanet:262803", "Benign partial epilepsy of infancy with complex partial seizures": "Orphanet:166299", "Ring chromosome 5": "Orphanet:251043", "Syndromic obesity": "Orphanet:240371", "Splenic Marginal Zone Lymphoma": "EFO:1000550", "HT1080": "EFO:0002059", "SPO": "EFO:0007033", "SARS coronavirus": "NCBITaxon:227859", "dantrolene": "CHEBI:4317", "fibromatosis": "EFO:0000497", "CMA-03": "EFO:0006552", "Psychrobacter arcticus 273-4": "NCBITaxon:259536", "Giant Lymph Node Hyperplasia": "EFO:1001332", "Kyasanur forest disease virus": "NCBITaxon:33743", "diltiazem": "CHEBI:101278", "Generalized bulbospinal muscular atrophy": "Orphanet:206710", "Cheirospondyloenchondromatosis": "Orphanet:99647", "Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia": "Orphanet:276608", "Erysiphe necator {http": "NCBITaxon:52586", "Spondyloepiphyseal dysplasia, Nishimura type": "Orphanet:163649", "Triticum dicoccoides": "NCBITaxon:85692", "dementia": "HP:0000726", "isoflavone": "CHEBI:18220", "autoimmune disease": "EFO:0005140", "Appendix Villous Adenoma": "EFO:1000093", "Familial reactive perforating collagenosis": "Orphanet:79147", "keratosis": "EFO:1000720", "Cleft palate - stapes fixation - oligodontia": "Orphanet:2010", "femoral neck bone mineral density": "EFO:0007785", "ENCODE functional genome mapping": "EFO:0002925", "Hereditary mixed polyposis syndrome": "Orphanet:157794", "sperm": "CL:0000019", "Constitutional megaloblastic anemia with severe neurologic disease": "Orphanet:319651", "L-cysteine": "CHEBI:17561", "Monogenic disease with epilepsy": "Orphanet:166472", "Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay": "Orphanet:88643", "GM17181 {http": "CLO:0013755", "bronchial smooth muscle cell derived cell line": "EFO:0005736", "corolla development stage {http": "PO:0007604", "catalase measurement": "EFO:0008071", "experimental factor": "EFO:0000001", "Hypoglycemia": "HP:0001943", "Retinal Neoplasm": "EFO:1000509", "3-methyladipate(2-) {http": "CHEBI:86387", "genetic variation": "EFO:0004828", "Salmonella enterica subsp. enterica serovar Typhi str. CT18": "NCBITaxon:220341", "RPMI6666": "EFO:0002321", "infant cerebrospinal fluid volume measurement": "EFO:0008367", "Abdominal Aortic Aneurysm": "EFO:0004214", "Blepharophimosis - ptosis - esotropia - syndactyly - short stature": "Orphanet:2057", "Picea mariana": "NCBITaxon:3335", "Vibrio parahaemolyticus RIMD 2210633": "NCBITaxon:223926", "GM17841 {http": "CLO:0016527", "Pili gemini": "Orphanet:79492", "monensin A": "CHEBI:27617", "Primary dystonia, DYT13 type": "Orphanet:98807", "Vaginal neoplasm": "EFO:1001447", "HCC4006": "EFO:0003132", "Colon Burkitt Lymphoma": "EFO:1000182", "X-linked dominant chondrodysplasia punctata": "Orphanet:35173", "ocular vascular disease": "EFO:0005753", "HCC2688": "EFO:0006433", "mature CD8_alpha-negative CD11b-negative dendritic cell": "CL:0001002", "storage organ": "EFO:0000997", "MOLP-8": "EFO:0006654", "Custer headache": "HP:0012199", "response to topoisomerase inhibitor": "GO:0072758", "vegetative shoot apical meristem {http": "PO:0008016", "Pediococcus pentosaceus": "NCBITaxon:1255", "TSS Sequencing": "EFO:0008978", "(15Z)-12-oxophyto-10,15-dienoic acid": "CHEBI:15560", "T-cell leukemia": "EFO:0005592", "Pruritus": "HP:0000989", "Spinocerebellar ataxia type 40": "EFO:0009057", "Xq27.3q28 duplication syndrome": "Orphanet:261483", "MIDAS": "EFO:0008809", "CB306": "EFO:0004078", "intestinal pseudo-obstruction": "EFO:1000988", "Late-infantile/juvenile Krabbe disease": "Orphanet:206443", "orthostatic hypotension": "EFO:0005252", "GM08714": "EFO:0005333", "Progressive pseudorheumatoid arthropathy of childhood": "Orphanet:1159", "amyloidoma": "EFO:1001874", "Blepharophimosis-intellectual disability syndrome, MKB type": "Orphanet:293707", "hormone role": "EFO:0001824", "xanthoma": "EFO:0003075", "neocarzinostatin chromophore": "CHEBI:29655", "Keipert syndrome": "Orphanet:2662", "granular eminence": "UBERON:2000212", "diaphragm disease": "EFO:0007233", "scRC-Seq": "EFO:0008912", "juvenile stage": "UBERON:0034919", "Lachancea kluyveri NRRL Y-12651": "NCBITaxon:226302", "susceptibility to urinary tract infection measurement": "EFO:0008413", "Bifidobacterium breve UCC2003": "NCBITaxon:326426", "T-helper 9 cell": "CL:0002061", "skin fluorescence measurement": "EFO:0005766", "ChIP-chip by SNP array": "EFO:0002764", "Disorder of methionine cycle and sulfur amino acid metabolism": "Orphanet:79173", "meningeal tuberculosis": "EFO:1000039", "Gossypium tomentosum": "NCBITaxon:34277", "GM17286 {http": "CLO:0013086", "amitrole": "CHEBI:40036", "Bladder Small Cell Neuroendocrine Carcinoma": "EFO:1000129", "Secondary polycythemia": "Orphanet:98428", "Coronaviridae infectious disease": "EFO:0007223", "Progressive familial intrahepatic cholestasis": "Orphanet:172", "corneal topography": "EFO:0004345", "SUM190PT": "EFO:0001243", "Cervical Mucinous Adenocarcinoma, Minimal Deviation Variant": "EFO:1000169", "Congenital vascular bone syndrome": "Orphanet:235832", "Disorder of multiple glycosylation": "Orphanet:309526", "Streptosporangium roseum": "NCBITaxon:2001", "Classical homocystinuria": "Orphanet:394", "Proximal 16p11.2 microduplication syndrome": "Orphanet:370079", "Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome": "Orphanet:404437", "Hydrocephalus - costovertebral dysplasia - Sprengel anomaly": "Orphanet:2180", "exon": "EFO:0004423", "MeRIP-Seq": "EFO:0008803", "Giant axonal neuropathy": "Orphanet:643", "Alobar holoprosencephaly": "Orphanet:93925", "extracutaneous mastocytoma": "EFO:1000932", "glycerol {http": "CHEBI:17754", "Congenital vitamin K-dependent coagulation factors deficiency": "Orphanet:169826", "GM17119 {http": "CLO:0014942", "abnormality of iron homeostasis": "HP:0011031", "Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency": "Orphanet:319543", "chronic progressive multiple sclerosis": "EFO:0003840", "ILSXISS99/TejJ": "EFO:0003002", "acromegaly": "EFO:1001485", "HEC1A": "EFO:0002191", "Salivary Gland Adenosquamous Carcinoma": "EFO:1000514", "cardiovascular disease": "EFO:0000319", "Cronkhite-Canada syndrome": "Orphanet:2930", "Van der Woude syndrome": "Orphanet:888", "growth hormone": "CHEBI:37845", "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations": "Orphanet:319462", "body proper": "UBERON:0013702", "F9 mouse embryonal carcinoma cell line": "EFO:0002053", "Cryptococcus neoformans var. grubii": "NCBITaxon:178876", "Saldino-Mainzer syndrome": "Orphanet:140969", "Manihot esculenta": "NCBITaxon:3983", "Carica papaya": "NCBITaxon:3649", "anther {http": "PO:0009066", "macroglobulinemia": "EFO:0002616", "Mastodynia": "EFO:1001366", "dry eye syndrome": "EFO:1000906", "presumptive rhombomere 8": "UBERON:0007295", "RBA-2 cell": "BTO:0002599", "HuT78": "EFO:0002209", "Xanthomonas oryzae pv. oryzae": "NCBITaxon:64187", "Swiss8": "EFO:0006302", "lethal midline granuloma": "EFO:1001013", "Carcinus maenas": "NCBITaxon:6759", "Rare syndrome with cardiac malformations": "Orphanet:156532", "erythrocyte differentiation": "GO:0030218", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A": "Orphanet:100043", "adaxial cells": "ZFA:0000003", "arterial occlusive disease": "EFO:0009085", "central retinal vein": "UBERON:0001673", "methionine": "CHEBI:16811", "Congenital absence of upper arm and forearm with hand present, bilateral": "Orphanet:295087", "rheumatic heart disease": "EFO:1001161", "Leukoencephalopathy with brain stem and spinal cord involvement - high lactate": "Orphanet:137898", "Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells": "Orphanet:331232", "Spinal Osteophytosis": "EFO:1001846", "carotid-femoral pulse wave velocity": "EFO:0004724", "diphyllobothriasis": "EFO:0007238", "Craniorachischisis": "Orphanet:63260", "iPS DF 19.11": "EFO:0007096", "berylliosis": "EFO:0007168", "Abruzzo-Erickson syndrome": "Orphanet:921", "GM1 gangliosidosis type 3": "Orphanet:79257", "46,XX ovotesticular disorder of sex development": "Orphanet:2138", "Mitochondrial protein import disorder": "Orphanet:254834", "Ws-3": "EFO:0005159", "high content screen": "EFO:0007550", "Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature": "Orphanet:307804", "Cerebrotendinous xanthomatosis": "Orphanet:909", "CS57621": "EFO:0000038", "Autosomal dominant polycystic kidney disease": "EFO:1001496", "TIVE": "EFO:0002086", "Immunodeficiency due to ficolin3 deficiency": "Orphanet:331190", "viral conjunctivitis": "EFO:0008571", "Progressive sensorineural hearing loss - hypertrophic cardiomyopathy": "Orphanet:228012", "dihomo-gamma-linolenic acid measurement": "EFO:0007763", "Granulocytic Sarcoma": "EFO:1000286", "Severe hemophilia A": "Orphanet:169802", "megagametophyte {http": "PO:0025279", "aluminium hydroxide": "CHEBI:33130", "Familial short QT syndrome": "Orphanet:51083", "Partial deletion of the short arm of chromosome 12": "Orphanet:316244", "ocular posterior capsular rupture": "EFO:1001817", "Sickle cell - beta-thalassemia disease": "Orphanet:251359", "lisinopril": "CHEBI:43755", "bronchus": "UBERON:0002185", "Spastic paraplegia - neuropathy - poikiloderma": "Orphanet:2821", "ocular motility disease": "EFO:1001990", "Hypoplastic amelogenesis imperfecta": "Orphanet:100031", "NCI-H2052": "EFO:0002275", "uric acid measurement": "EFO:0004761", "Nephrogenic diabetes insipidus": "Orphanet:223", "Emery-Dreifuss muscular dystrophy": "Orphanet:261", "labetalol": "CHEBI:6343", "bone measurement": "EFO:0004512", "cognitive function measurement": "EFO:0008354", "Multiple congenital anomalies - hypotonia - seizures syndrome": "Orphanet:280633", "Xp22.13p22.2 duplication syndrome": "Orphanet:284180", "IgM plasma cell": "CL:0000986", "Rare hereditary ataxia": "Orphanet:183518", "root structure": "EFO:0000989", "Late-onset ataxia with dementia": "Orphanet:98540", "Glomuvenous malformation": "Orphanet:83454", "plant component": "EFO:0000789", "GM17162 {http": "CLO:0013983", "Qualitative or quantitative defects of beta-myosin heavy chain (MYH7)": "Orphanet:209185", "Autosomal recessive cerebellar ataxia - psychomotor retardation": "Orphanet:284271", "Paramyotonia congenita of Von Eulenburg": "Orphanet:684", "diquat": "CHEBI:64163", "Trypanosoma brucei": "NCBITaxon:5691", "Craniosynostosis - dysmorphism - brachydactyly": "Orphanet:1535", "Southeast Asian ovalocytosis": "Orphanet:98868", "D-2-hydroxyglutaric aciduria": "Orphanet:79315", "Folinic acid-responsive seizures": "Orphanet:79097", "ILSXISS123/TejJ": "EFO:0003012", "Blepharophimosis-intellectual disability syndrome, SBBYS type": "Orphanet:3047", "Odonto-onycho dysplasia - alopecia": "Orphanet:2722", "Griscelli disease type 2": "Orphanet:79477", "glossitis": "EFO:1000951", "ascaridiasis": "EFO:0007155", "parous": "EFO:0002947", "consortium member": "EFO:0001731", "Alopecia-contractures-dwarfism-intellectual disability syndrome": "Orphanet:1005", "ovarian cystadenocarcinoma": "EFO:1001962", "Pachycladon novaezelandiae": "NCBITaxon:106788", "aphthous ulcer": "EFO:0003938", "NCI-H810": "EFO:0002305", "Copenhagen": "EFO:0001344", "Brain demyelination due to methionine adenosyltransferase deficiency": "Orphanet:168598", "GM07000": "EFO:0001110", "Abnormality of esophagus morphology {http": "HP:0002031", "GM11831": "EFO:0001119", "Coloboma of optic papilla": "Orphanet:98947", "Autosomal recessive Charcot Marie Tooth disease type 2X": "EFO:1001983", "hamartoma": "EFO:1000634", "Noonan syndrome and Noonan-related syndrome": "Orphanet:98733", "Anemia, Hemolytic, Autoimmune": "EFO:1001264", "Lowry-MacLean syndrome": "Orphanet:2409", "CD34-negative, GlyA-negative proerythroblast": "CL:0002004", "Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome": "Orphanet:369837", "Congenital heart block": "Orphanet:60041", "GM14409 {http": "CLO:0031226", "Peroxisomal beta-oxidation disorder": "Orphanet:79188", "Coxiella burnetii": "NCBITaxon:777", "UMP-CMP kinase measurement": "EFO:0008313", "large cell medulloblastoma": "EFO:0008508", "CD1a-positive dermal dendritic cell": "CL:0002529", "3-sulfino-L-alanine {http": "CHEBI:16345", "Senecio vulgaris subsp. vulgaris": "NCBITaxon:121558", "glucagon-like peptide-1 measurement": "EFO:0008465", "ovarian serous carcinoma": "EFO:1001516", "opercular lateral line neuromast": "UBERON:2000814", "response to heparin": "EFO:0006816", "Clark level II": "EFO:0004958", "division of carotid artery": "EFO:0001954", "sporocyte {http": "PO:0006204", "Brain atrophy {http": "HP:0012444", "stamen primordium visible stage {http": "PO:0007613", "Autosomal recessive dopa-responsive dystonia": "Orphanet:101150", "distal colitis": "EFO:0005623", "Distal hereditary motor neuropathy type 7": "Orphanet:139589", "Congenital hypothyroidism": "Orphanet:442", "Strongyloides ratti": "NCBITaxon:34506", "Neonatal acute respiratory distress with surfactant metabolism deficiency": "Orphanet:217563", "HFF-Myc": "EFO:0005710", "atrial tachycardia": "EFO:0005308", "LDL cholesteriol": "EFO:0007930", "Gastroduodenal malformation": "Orphanet:97944", "Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions": "EFO:1000508", "reading and spelling ability": "EFO:0005301", "helping behavior measurement": "EFO:0008538", "embryonic cell line": "EFO:0003040", "Macaca nemestrina": "NCBITaxon:9545", "Stevens-Johnson syndrome": "EFO:0004276", "anti-citrullinated protein antibody seropositivity": "EFO:0007837", "Intellectual disability - balding - patella luxation - acromicria": "Orphanet:3041", "severe aplastic anemia": "EFO:0006927", "reduce cholesterol levels": "EFO:0004456", "Distal monosomy 3p": "Orphanet:1620", "Familial recurrent peripheral facial palsy": "Orphanet:2809", "movement disorder": "EFO:0004280", "Pestivirus infectious disease": "EFO:0007432", "Acral self-healing collodion baby": "Orphanet:281127", "basic fibroblast growth factor": "EFO:0003316", "BDCM": "EFO:0002113", "decanoate {http": "CHEBI:27689", "seed coat {http": "PO:0009088", "biopsy site": "EFO:0000288", "reasoning": "EFO:0004350", "X-linked intellectual disability, Wilson type": "Orphanet:85290", "iron biomarker measurement": "EFO:0004461", "Prominent forehead {http": "HP:0011220", "Ovarian Serous Adenocarcinofibroma": "EFO:1000427", "ABC-1": "EFO:0002813", "cellular metabolic process": "GO:0044237", "macrophage": "CL:0000235", "End Stage Liver Disease": "EFO:1001311", "Delayed membranous cranial ossification": "Orphanet:3034", "epidermal cell": "CL:0000362", "Pulmonary venoocclusive disease": "Orphanet:31837", "Wolf-Hirschhorn syndrome": "Orphanet:280", "Bacillus amyloliquefaciens": "NCBITaxon:1390", "mNET-seq": "EFO:0008819", "Oligocone trichromacy": "Orphanet:75378", "LA-N-1": "EFO:0005391", "autism spectrum disorder symptom": "EFO:0005426", "array control spike calibration": "EFO:0000375", "Hyper-IgM syndrome with susceptibility to opportunistic infections": "Orphanet:183663", "Panc1": "EFO:0002713", "Mitochondrial DNA depletion syndrome, hepatocerebral form": "Orphanet:254871", "potassium nitrate": "CHEBI:63043", "46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect": "Orphanet:90786", "LK-2": "EFO:0003141", "primary Fusobacteriaceae infectious disease": "EFO:1001126", "Syndrome associated with hypertrophic cardiomyopathy": "Orphanet:217595", "WM793-P2N1": "EFO:0002875", "Primary hypergonadotropic hypogonadism - partial alopecia": "Orphanet:2232", "Sinorhizobium meliloti": "NCBITaxon:382", "assay by array": "EFO:0002696", "embryonic stomatogastric nervous system": "FBbt:00001069", "Madelung deformity": "Orphanet:35688", "Constitutional neutropenia with extra-haematopoietic manifestations": "Orphanet:331184", "Unclassified primitive or secondary maculopathy": "Orphanet:98666", "Juvenile polyposis syndrome": "Orphanet:2929", "atrial appendage": "UBERON:0006618", "Pseudoprogeria syndrome": "Orphanet:2985", "inbred": "EFO:0004429", "Clonorchis sinensis": "NCBITaxon:79923", "eosinophilic myeloblast": "CL:0000832", "IgG disialylation measurement": "EFO:0008429", "Duodenal Villous Adenoma": "EFO:1000225", "Classic lissencephaly": "Orphanet:102009", "miotic rate": "EFO:0007057", "macula measurement": "EFO:0008375", "Symptomatic form of hemophilia B in female carriers": "Orphanet:177929", "Paternal uniparental disomy of chromosome 21": "Orphanet:96195", "metastatic melanoma": "EFO:0002617", "kidney cortex necrosis": "EFO:1001003", "GM17295 {http": "CLO:0013127", "bone mineral content measurement": "EFO:0007621", "food allergy": "EFO:1001890", "GM06994": "EFO:0001109", "Abnormality of the intestine": "HP:0002242", "UV light regimen {http": "EO:0007222", "Abnormality of muscle size": "HP:0030236", "bacteriemia": "EFO:0003033", "Ring chromosome 16": "Orphanet:96178", "urinary S-phenylmercapturic acid measurement": "EFO:0007651", "Benign Ovarian Brenner Tumor": "EFO:1000112", "Charcot-Marie-Tooth disease type 4G": "Orphanet:99953", "Autosomal recessive hereditary sensory and autonomic neuropathy": "Orphanet:140477", "ependymal cell": "CL:0000065", "cotyledon {http": "PO:0020030", "primary cell": "EFO:0002660", "blind loop syndrome": "EFO:0007175", "antiseptic drug": "CHEBI:48218", "mature ovarian follicle": "UBERON:0003982", "Myofibroma": "EFO:1000389", "Late-onset retinal degeneration": "Orphanet:67042", "Mucocutaneous venous malformations": "Orphanet:2451", "response to darapladib": "EFO:0008395", "Jalili syndrome": "Orphanet:1873", "Diencephalic-mesencephalic junction dysplasia": "Orphanet:319192", "Cobblestone lissencephaly": "Orphanet:51577", "COR-L26": "EFO:0006555", "Trigonocephaly - bifid nose - acral anomalies": "Orphanet:3368", "Stromal corneal dystrophy": "Orphanet:98626", "Candida albicans": "NCBITaxon:5476", "complement decay-accelerating factor measurement": "EFO:0008095", "Intellectual disability, mild {http": "HP:0001256", "Acromesomelic dysplasia, Hunter-Thomson type": "Orphanet:968", "Brachydactyly - long thumb": "Orphanet:2946", "MDAMB231": "EFO:0001209", "GM17815 {http": "CLO:0016506", "D10.G4.1": "EFO:0002822", "parathyroid hormone measurement": "EFO:0004752", "Spondylometaphyseal dysplasia, 'corner fracture' type": "Orphanet:93315", "Hermansky-Pudlak syndrome": "Orphanet:79430", "Pierre Robin syndrome associated with branchial archs anomalies": "Orphanet:138050", "apical ectodermal ridge dorsal fin": "UBERON:2000090", "MDS": "EFO:0008801", "fetal erythroblastosis": "EFO:1000937", "Qualitative or quantitative defects of sarcoglycan": "Orphanet:207052", "sleep apnea measurement": "EFO:0007817", "last follow up": "EFO:0007058", "Muckle-Wells syndrome": "Orphanet:575", "antibacterial drug": "CHEBI:36047", "lateral floor plate": "UBERON:2001256", "Lung agenesis - heart defect - thumb anomalies": "Orphanet:1120", "CD115-positive monocyte": "CL:0001022", "Genetic 46,XY disorder of sex development": "Orphanet:325706", "Seborrhea-like dermatitis with psoriasiform elements": "Orphanet:168606", "Nasopalpebral lipoma - coloboma - telecanthus": "Orphanet:2399", "aplastic anemia": "HP:0001915", "NUT midline carcinoma": "EFO:0005783", "Macrodactyly of toes, bilateral": "Orphanet:295245", "HCC1599": "EFO:0002186", "Strombus gigas": "NCBITaxon:291982", "MARDI": "EFO:0008794", "genotype design": "EFO:0001748", "delta-5 desaturase measurement": "EFO:0007764", "optic nerve": "FBbt:00001956", "Brain-lung-thyroid syndrome": "Orphanet:209905", "Alpha-1-antichymotrypsin deficiency": "Orphanet:93594", "adrenocorticotropic hormone": "CHEBI:3892", "array surface coating": "EFO:0005069", "GM17194 {http": "CLO:0013798", "Isolated congenital alacrima": "Orphanet:91416", "CD38-positive unswitched memory B cell": "CL:0002114", "Corynebacterium jeikeium": "NCBITaxon:38289", "VirCapSeq-VERT": "EFO:0008982", "benzenetriols": "CHEBI:22707", "partial motor epilepsy": "EFO:1001089", "GM17124 {http": "CLO:0015121", "complement component C7 measurement": "EFO:0008093", "Pharyngeal Adenoid Cystic Carcinoma": "EFO:1000472", "formaldehyde": "CHEBI:16842", "low-density lipoprotein": "CHEBI:39026", "Osteosclerosis - ichthyosis - premature ovarian failure": "Orphanet:75325", "inferior myocardial infarction": "EFO:1000983", "X-linked recessive ocular albinism": "Orphanet:54", "quinate {http": "CHEBI:26490", "HOP62": "EFO:0006439", "CD27 antigen measurement": "EFO:0008078", "Paternal uniparental disomy of chromosome 20": "Orphanet:96194", "rheumatic disease": "EFO:0005755", "ammonium nitrate": "CHEBI:63038", "Progressive epilepsy - intellectual disability, Finnish type": "Orphanet:1947", "posterior endoderm anlage": "FBbt:00000447", "Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome": "Orphanet:363741", "Salmonella enterica subsp. enterica serovar Agona": "NCBITaxon:58095", "single-multicellular organism process": "GO:0044707", "CS57580": "EFO:0000020", "umbilical vein": "UBERON:0002066", "MN9D": "EFO:0006455", "serum non-albumin protein measurement": "EFO:0004568", "Bm2 B cell": "CL:0000962", "GM17806 {http": "CLO:0016505", "band form neutrophil": "CL:0000560", "bone marrow macrophage": "CL:0002476", "Porphyria variegata": "Orphanet:79473", "Severe early-childhood-onset retinal dystrophy": "Orphanet:364055", "extracellular organelle": "GO:0043230", "cross sectional design": "EFO:0001428", "NCI-H1781": "EFO:0006663", "PEO23": "EFO:0005447", "Caenorhabditis": "NCBITaxon:6237", "oleamide {http": "CHEBI:116314", "waist-hip ratio": "EFO:0004343", "susceptibility to mononucleosis measurement": "EFO:0008403", "CLASH": "EFO:0008693", "AG07307 {http": "CLO:0035579", "erythroid progenitor cell": "CL:0000038", "response to cytarabine": "GO:0097331", "Lumbosacral spina bifida aperta": "Orphanet:268388", "exanthem": "EFO:1000697", "menopause": "EFO:0003922", "Hexadecanoic acid": "CHEBI:15756", "5q35 microduplication syndrome": "Orphanet:228415", "muscarinic antagonist": "CHEBI:48876", "Alzheimer's disease biomarker measurement": "EFO:0006514", "malignant": "EFO:0006851", "chylomicron measurement": "EFO:0008596", "hippocampus CA4": "UBERON:0003884", "abdominal fibromatosis": "EFO:1001325", "G118": "EFO:0006397", "N-isobutyrylglycine {http": "CHEBI:70979", "Acromegaloid facial appearance syndrome": "Orphanet:965", "hairy tongue": "EFO:1000957", "Quebec platelet disorder": "Orphanet:220436", "neurofibrilliary tangles measurement": "EFO:0006797", "BALB/c": "EFO:0000602", "Spinocerebellar ataxia with epilepsy": "Orphanet:254881", "Adams-Oliver syndrome": "Orphanet:974", "CB155": "EFO:0004075", "Pachycladon": "NCBITaxon:106787", "mammographic density measurement": "EFO:0005941", "Panniculitis, Peritoneal": "EFO:1001384", "Maternal uniparental disomy of chromosome 22": "Orphanet:96188", "Pancreatic Acinar Cell Carcinoma": "EFO:1000439", "Karsch-Neugebauer syndrome": "Orphanet:2329", "cytokine": "EFO:0003786", "Epithelial recurrent erosion dystrophy": "Orphanet:293381", "floral organ formation stage {http": "PO:0025585", "skin pigmentation": "EFO:0003784", "longevity": "EFO:0004300", "Rare familial disorder with hypertrophic cardiomyopathy": "Orphanet:99739", "natural killer cell": "CL:0000623", "Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia": "Orphanet:253", "Pantoea stewartii": "NCBITaxon:66269", "mature CD8 single-positive thymocyte": "CL:0002437", "Abnormality of muscle morphology": "HP:0011805", "Plasmodium yoelii": "NCBITaxon:5861", "2-deoxy-D-glucose": "CHEBI:15866", "Primary intestinal lymphangiectasia": "Orphanet:90362", "early lymphoid progenitor": "CL:0000936", "specimen": "OBI:0100051", "papillary cystadenocarcinoma": "EFO:0000639", "Autosomal recessive systemic lupus erythematosus": "Orphanet:300345", "CD11c-negative plasmacytoid dendritic cell": "CL:0000991", "large artery stroke": "EFO:0005524", "HaCaT": "EFO:0002056", "Ethmoid Sinus Adenoid Cystic Carcinoma": "EFO:1000246", "eye disc": "FBbt:00001768", "GM14453 {http": "CLO:0031253", "HuH-7.5": "EFO:0005704", "Eyelid malformation": "Orphanet:98561", "CB4854": "EFO:0004053", "angiotensin-converting enzyme measurement": "EFO:0006515", "PAT-Seq": "EFO:0008851", "amniotic fluid embolism {http": "EFO:1001263", "(E)-clothianidin": "CHEBI:39177", "Musa sp.": "NCBITaxon:46838", "renal carcinoma": "EFO:0002890", "NCI-H146": "EFO:0006659", "Floating-Harbor syndrome": "Orphanet:2044", "Familial juvenile hyperuricemic nephropathy type 1": "Orphanet:209886", "3-phenylpropionate {http": "CHEBI:51057", "NCI-H747": "EFO:0002303", "Trichothiodystrophy": "Orphanet:33364", "Leishmaniasis": "EFO:0005044", "Sch\u00c3\u00b6pf-Schulz-Passarge syndrome": "Orphanet:50944", "Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis": "Orphanet:93217", "Methanococcus": "NCBITaxon:2184", "Papio": "NCBITaxon:9554", "neurofibromatosis": "EFO:0008514", "Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor": "EFO:1000250", "GM17116 {http": "CLO:0014953", "Rare constitutional anemia": "Orphanet:183651", "total fat intake measurement": "EFO:0007678", "OX-2 membrane glycoprotein measurement": "EFO:0008253", "BHY": "EFO:0006539", "blastula dome": "EFO:0001279", "metabolite role": "CHEBI:25212", "Intellectual disability {http": "HP:0001249", "ventricular zone": "UBERON:0003053", "2b-RAD": "EFO:0008638", "fibrosarcoma": "EFO:0002087", "quantitative confidence value": "OBI:0000071", "smooth muscle myoblast": "CL:0000514", "Fibroadenoma": "EFO:1000254", "atrophy of thyroid": "EFO:1000827", "fenofibrate": "CHEBI:5001", "forehead morphology measurement": "EFO:0007844", "lipoprotein": "EFO:0003836", "Maternal uniparental disomy of chromosome X": "Orphanet:261519", "hypopharynx cancer": "EFO:0007321", "X-linked intellectual disability, Shrimpton type": "Orphanet:85324", "CD4-negative, CD8-negative, alpha-beta intraepithelial T cell": "CL:0000935", "cerebral toxoplasmosis": "EFO:0007200", "GM11992": "EFO:0001124", "SUM185PE": "EFO:0001242", "Disorder of glutamine metabolism": "Orphanet:289841", "hematopoietic cell": "CL:0000988", "2.03 main shoot and axillary shoots visible at three nodes stage {http": "PO:0007080", "Drop-ChIP": "EFO:0008721", "RNA-seq of coding RNA from single cells": "EFO:0005684", "5q14.3 microdeletion syndrome": "Orphanet:228384", "Reticular dysgenesis": "Orphanet:33355", "Ribes nigrum": "NCBITaxon:78511", "L-1210": "EFO:0005284", "CLaP": "EFO:0008692", "Leptospira interrogans serovar Lai": "NCBITaxon:57678", "cellular response to abiotic stimulus": "GO:0071214", "SiHa": "EFO:0002379", "Oryza longistaminata": "NCBITaxon:4528", "SW962": "EFO:0002377", "LXFL529": "EFO:0006642", "keratoconjunctivitis sicca": "EFO:1001001", "lymph node subcapsular sinus macrophage": "CL:0000887", "embryonic stage 2": "EFO:0005861", "Juvenile cataract - microcornea - renal glucosuria": "Orphanet:247794", "nucleoside phosphate metabolic process": "GO:0006753", "presumptive midbrain": "UBERON:0009616", "Palmar Fibromatosis": "EFO:1000438", "organelle": "GO:0043226", "systemic inflammatory response syndrome": "EFO:1001478", "GM17758 {http": "CLO:0016608", "Rhodococcus jostii RHA1": "NCBITaxon:101510", "Attached earlobe": "HP:0009907", "Anonychia - microcephaly": "Orphanet:1094", "neutropenic enterocolitis": "EFO:1001816", "Autosomal dominant Charcot-Marie-Tooth disease type 2J": "Orphanet:99943", "Spondylometaphyseal dysplasia, Golden type": "Orphanet:168544", "Rothmund-Thomson syndrome": "Orphanet:2909", "GM17113 {http": "CLO:0014943", "Cecum Villous Adenoma": "EFO:1000155", "Isolated focal cortical dysplasia type Ia": "Orphanet:268973", "Congenital myotonia": "Orphanet:206973", "Hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism": "Orphanet:289494", "Familial Scheuermann disease": "Orphanet:3135", "mesenchymal chondrosarcoma": "EFO:1001041", "obsessive-compulsive symptom measurement": "EFO:0007802", "supraoptic nucleus": "UBERON:0001929", "SD": "EFO:0007027", "Salmonella enterica subsp. enterica serovar Paratyphi C": "NCBITaxon:57046", "spinal subdural hematoma": "EFO:1001847", "leptin": "EFO:0003199", "response to CAPOX-B": "EFO:0007683", "Isolated focal cortical dysplasia": "Orphanet:65683", "WGBS": "EFO:0008985", "X-linked Charcot-Marie-Tooth disease type 3": "Orphanet:101077", "DeepCAGE": "EFO:0008708", "AG09877 {http": "CLO:0021943", "Patterson-Stevenson-Fontaine syndrome": "Orphanet:2439", "Cucumis sativus": "NCBITaxon:3659", "Citrus trifoliata": "NCBITaxon:37690", "Radio-ulnar synostosis, bilateral": "Orphanet:295219", "Saccharomyces bayanus": "NCBITaxon:4931", "Non-syndromic male infertility due to sperm motility disorder": "Orphanet:276234", "vertical myoseptum": "UBERON:2000610", "tracheitis": "EFO:0007518", "Campomelic dysplasia": "Orphanet:140", "density unit": "UO:0000182", "serum metabolite measurement": "EFO:0005653", "Primary bone dysplasia with disorganized development of skeletal components": "Orphanet:93450", "Short stature due to growth hormone qualitative anomaly": "Orphanet:629", "Immunodeficiency by defective expression of HLA class 2": "Orphanet:572", "atherosclerosis": "EFO:0003914", "Adenofibroma": "EFO:1000070", "X-linked spastic paraplegia type 16": "Orphanet:100997", "COG4-CDG": "Orphanet:263501", "Hereditary coproporphyria": "Orphanet:79273", "olmesartan": "CHEBI:48416", "suberate(2-) {http": "CHEBI:76282", "normal cell line": "EFO:0002922", "optic disc size measurement": "EFO:0004832", "Sg4": "EFO:0005839", "bronchial smooth muscle cell": "CL:0002598", "umbilical cord blood": "UBERON:0012168", "interleukin 6 receptor subunit beta measurement": "EFO:0008188", "Partial deletion of the short arm of chromosome 10": "Orphanet:261938", "hip osteoarthritis symptom severity measurement": "EFO:0007942", "fat body primordium": "FBbt:00005067", "Glycine encephalopathy": "Orphanet:407", "leptin receptor measurement": "EFO:0004635", "GM14474 {http": "CLO:0031280", "Parastremmatic dwarfism": "Orphanet:2646", "Non-spherocytic hemolytic anemia due to hexokinase deficiency": "Orphanet:90031", "capitellum": "FBbt:00004784", "WKY": "EFO:0001351", "lithium chloride": "CHEBI:48607", "3-hydroxy-3-methylglutaric aciduria": "Orphanet:20", "Hydrocephalus - blue sclerae - nephropathy": "Orphanet:2186", "blastomycosis": "EFO:0007174", "lower urinary tract symptom": "EFO:0008008", "Progressive deafness with stapes fixation": "Orphanet:3235", "arm span": "EFO:0005108", "Caudal regression sequence": "Orphanet:3027", "Marsilea quadrifolia": "NCBITaxon:13816", "Microcephaly - polymicrogyria - corpus callosum agenesis": "Orphanet:171703", "lentiform nucleus measurement": "EFO:0004913", "Progressive cavitating leukoencephalopathy": "Orphanet:139447", "abortion": "EFO:1001491", "unit": "UO:0000000", "Autosomal recessive ataxia due to PEX10 deficiency": "Orphanet:247815", "Genetic dermis elastic tissue disorder": "Orphanet:228215", "vascular leaf {http": "PO:0009025", "Micromelic dwarfism, Fryns type": "Orphanet:2641", "Major induction processes eye anomaly": "Orphanet:98554", "Tr1 cell": "CL:0000901", "Vitamin B12-responsive methylmalonic acidemia, type cblDv2": "Orphanet:308442", "Mesial temporal lobe epilepsy with hippocampal sclerosis": "Orphanet:99701", "picomole per 10^6 cells": "EFO:0004388", "Congenital muscular dystrophy, Fukuyama type": "Orphanet:272", "Endosteal sclerosis - cerebellar hypoplasia": "Orphanet:85186", "Susac Syndrome": "EFO:1001856", "adrenal cortex carcinoma": "EFO:1000796", "GM5659": "EFO:0006278", "Sulfolobus solfataricus": "NCBITaxon:2287", "Autosomal dominant aplasia and myelodysplasia": "Orphanet:314399", "bile duct": "UBERON:0002394", "optimization design": "EFO:0001773", "mature alpha-beta T cell": "CL:0000791", "transport vesicle membrane": "GO:0030658", "CAB-Seq": "EFO:0008668", "sodium tungstate dihydrate": "CHEBI:63939", "Short stature, Brussels type": "Orphanet:2867", "Neurogenic bladder": "HP:0000011", "arteriosclerosis": "EFO:0009086", "OV56": "EFO:0006458", "arterial stiffness measurement": "EFO:0004517", "self reported educational attainment": "EFO:0004784", "RNA interference": "GO:0016246", "hemocyte": "CL:0000387", "Lilium hybrid division I": "NCBITaxon:156532", "Bartonella henselae": "NCBITaxon:38323", "Tumor necrosis factor receptor 1 associated periodic syndrome": "Orphanet:32960", "mesothelial neoplasm": "EFO:1001044", "(S)-(-)-sulpiride": "CHEBI:64119", "MHPG measurement": "EFO:0005133", "Genetic skeletal muscle disease": "Orphanet:206634", "Diastrophic dwarfism": "Orphanet:628", "pars intercerebralis primordium": "FBbt:00005511", "Infantile neuroaxonal dystrophy": "Orphanet:35069", "Familial dementia, Danish type": "Orphanet:97346", "Congenital muscular dystrophy due to dystroglycanopathy": "Orphanet:370953", "Bruguiera gymnorhiza": "NCBITaxon:39984", "Acinar Prostate Adenocarcinoma, Foamy Gland Variant": "EFO:1000064", "Bm3 B cell": "CL:0000965", "large adipocyte": "EFO:0002572", "Severe achondroplasia - developmental delay - acanthosis nigricans": "Orphanet:85165", "Phalaenopsis aphrodite subsp. formosana": "NCBITaxon:308872", "anal neoplasm": "EFO:0003835", "concentration dose ratio": "EFO:0007635", "Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type": "Orphanet:217026", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C": "Orphanet:100045", "congestive heart failure": "EFO:0000373", "Auriculoocular anomalies - cleft lip": "Orphanet:71270", "Choristoneura fumiferana MNPV": "NCBITaxon:208973", "Autoimmune lymphoproliferative syndrome with recurrent viral infections": "Orphanet:275517", "atrazine": "CHEBI:15930", "Congenital or early infantile CACH syndrome": "Orphanet:157713", "GM17739 {http": "CLO:0017022", "2,3,7,8-tetrachlorodibenzodioxine": "CHEBI:28119", "Spondylocostal dysostosis - hypospadias - intellectual disability": "Orphanet:329252", "Salmonella enterica subsp. enterica serovar Typhimurium str. LT2": "NCBITaxon:99287", "Familial hyperreninemic hypoaldosteronism type 1": "Orphanet:99763", "Aplysia californica": "NCBITaxon:6500", "Multicentric osteolysis-nodulosis-arthropathy spectrum": "Orphanet:371428", "amygdala reactivity measurement": "EFO:0004550", "enteric nervous system": "UBERON:0002005", "Caulobacter crescentus NA1000": "NCBITaxon:565050", "GM06985": "EFO:0001107", "Macular corneal dystrophy": "Orphanet:98969", "clusterin measurement": "EFO:0007655", "TBP-71Q-16": "EFO:0001338", "Normosmic congenital hypogonadotropic hypogonadism": "Orphanet:432", "GM17827 {http": "CLO:0016528", "Kimura disease": "EFO:1000722", "illegal drug consumption": "EFO:0005431", "TN-Seq": "EFO:0008973", "L-prolylglycine {http": "CHEBI:61695", "Refsum disease": "Orphanet:773", "endometrial endometrioid adenocarcinoma, variant with squamous differentiation": "EFO:1001953", "sporophyte development stage": "PO:0028002", "GM12874": "EFO:0001161", "Rare genetic dystonia": "Orphanet:391799", "naproxen": "CHEBI:7476", "SUM149PT": "EFO:0001240", "uterine sarcoma": "EFO:0002914", "Beta-ureidopropionase deficiency": "Orphanet:65287", "monocyte-derived osteoclast": "EFO:0002666", "Syndrome associated with dilated cardiomyopathy": "Orphanet:217619", "uvula": "UBERON:0001734", "post-operative sensory disturbance": "EFO:0005324", "induced pluripotent stem cell": "EFO:0004905", "Abnormality of the corpus callosum {http": "HP:0001273", "array design": "EFO:0000269", "prostate derived cell line": "EFO:0002891", "Fusobacterium infectious disease": "EFO:1000943", "Lewis": "EFO:0001353", "Pseudoxanthoma elasticum": "Orphanet:758", "response to reverse transcriptase inhibitor": "GO:0061479", "RAP": "EFO:0008880", "GM14417 {http": "CLO:0031239", "Familial multiple lipomatosis": "Orphanet:199276", "Ankylosing vertebral hyperostosis with tylosis": "Orphanet:2206", "Pierson syndrome": "Orphanet:2670", "Schistocerca gregaria": "NCBITaxon:7010", "synapse": "GO:0045202", "symbiosis, encompassing mutualism through parasitism": "GO:0044403", "L-Selectin measurement": "EFO:0008202", "clobenpropit dihydrobromide": "CHEBI:64165", "CB88": "EFO:0004045", "GM17780 {http": "CLO:0016643", "cingulate cortex measurement": "EFO:0007738", "mature gamma-delta T cell": "CL:0000800", "biomolecular annotation design": "EFO:0004665", "Candidatus Pelagibacter ubique HTCC1062": "NCBITaxon:335992", "semaphorin-3A measurement": "EFO:0008278", "gestational diabetes": "EFO:0004593", "brain volume measurement": "EFO:0006930", "T wave morphology measurement": "EFO:0008398", "Potato virus X": "NCBITaxon:12183", "neutrophilic myeloblast": "CL:0000042", "JHH-4": "EFO:0006601", "Lower motor neuron syndrome with late-adult onset": "Orphanet:276435", "Thiomonas sp. 3As": "NCBITaxon:426114", "right atrium": "UBERON:0002078", "Von Hippel-Lindau disease": "Orphanet:892", "whole-brain volume": "EFO:0005089", "Bulbospinal muscular atrophy of children": "Orphanet:206704", "proteomic profiling by array": "EFO:0002765", "response to sotalol": "EFO:0008325", "genetic disorder": "EFO:0000508", "Caldicellulosiruptor bescii": "NCBITaxon:31899", "B-lymphoma cell line": "BTO:0001518", "Qualitative or quantitative defects of alpha-dystroglycan": "Orphanet:371024", "Syndromic hyperopia": "Orphanet:98622", "airway responsiveness measurement": "EFO:0006897", "Abnormality of the eye": "HP:0000478", "complement C4b measurement": "EFO:0008092", "Charcot-Marie-Tooth disease type 4E": "Orphanet:99951", "Charcot-Marie-Tooth disease type 2B1": "Orphanet:98856", "Hyperpigmentation of the skin": "EFO:0009047", "Rare genetic vascular disease": "Orphanet:233655", "Fibular hemimelia": "Orphanet:93323", "response to interferon beta": "GO:0035456", "2p21 microdeletion syndrome without cystinuria": "Orphanet:369881", "acoustic startle blink response measurement": "EFO:0006875", "14q11.2 microduplication syndrome": "Orphanet:261229", "susceptibility to rheumatic fever measurement": "EFO:0008416", "balding measurement": "EFO:0007825", "freckles": "EFO:0003963", "Genetic 46,XX disorder of sex development": "Orphanet:325697", "3 inflorescence detectable stage": "PO:0007047", "prefrontal cortex": "UBERON:0000451", "uterus": "UBERON:0000995", "Spartina alterniflora": "NCBITaxon:29706", "MCAS": "EFO:0006453", "eunuchism": "EFO:0007266", "Hepatitis, Alcoholic": "EFO:1001345", "Von Voss-Cherstvoy syndrome": "Orphanet:3439", "High palate {http": "HP:0000218", "GM17259 {http": "CLO:0014388", "Platyhelminthes adult": "EFO:0007715", "Hypocalcemic vitamin D-resistant rickets": "Orphanet:93160", "adenohypophysis": "UBERON:0002196", "Glycogen storage disease due to glucose-6-phosphatase deficiency": "Orphanet:364", "Tubular duplication of the esophagus": "Orphanet:100048", "docosahexaenoic acid measurement": "EFO:0007761", "pervasive developmental disorder - not otherwise specified": "EFO:0003759", "HuPT4": "EFO:0002208", "cerebral palsy": "EFO:1000632", "response to ranibizumab": "EFO:0008348", "Malignant Bladder Paraganglioma": "EFO:1000349", "Lactococcus lactis": "NCBITaxon:1358", "1-oleoylglycerol {http": "CHEBI:75342", "purine nucleoside triphosphate biosynthetic process": "GO:0009145", "GM14439 {http": "CLO:0031234", "pituitary dwarfism": "EFO:1001109", "disease staging": "EFO:0000410", "Obesity Hypoventilation Syndrome": "EFO:1001382", "plant sperm": "EFO:0001005", "type II diabetes mellitus": "EFO:0001360", "Ptosis - vocal cord paralysis": "Orphanet:2997", "methyl cellulose": "CHEBI:53448", "Poppelsdorf ecotype": "EFO:0006971", "lux": "UO:0000116", "1,10-phenanthroline": "CHEBI:44975", "Abnormality of dental enamel {http": "HP:0000682", "Ruminococcus": "NCBITaxon:1263", "Alpha-thalassemia-related diseases": "Orphanet:232288", "glycochenodeoxycholate {http": "CHEBI:36252", "in preparation": "EFO:0001795", "Blepharophimosis - epicanthus inversus - ptosis due to 3q23 microdeletion": "Orphanet:261559", "Qualitative or quantitative defects of beta-sarcoglycan": "Orphanet:207063", "Malignancy in Giant Cell Tumor of Bone": "EFO:1000347", "Hereditary continuous muscle fiber activity": "Orphanet:972", "Gr1-low non-classical monocyte": "CL:0002058", "Cerebro-facio-thoracic dysplasia": "Orphanet:1394", "Tuberculosis": "Orphanet:3389", "Ichthyosis - intellectual disability - dwarfism - renal impairment": "Orphanet:2278", "abnormal": "PATO:0000460", "malignant epithelioid mesothelioma": "EFO:0006452", "ticagrelor measurement": "EFO:0007007", "Encephalopathy due to sulfite oxidase deficiency": "Orphanet:833", "Nucleo-Seq": "EFO:0008836", "asparaginase hypersensitivity": "EFO:0004881", "CANDLE syndrome": "Orphanet:325004", "Terminal transverse defects of arm": "Orphanet:93937", "Dysmorphism - short stature - deafness - disorder of sex development": "Orphanet:2282", "liposarcoma": "EFO:0000569", "Mitochondrial oxidative phosphorylation disorder with no known mechanism": "Orphanet:254822", "renal nutcracker syndrome": "EFO:1001838", "CS57822": "EFO:0000130", "succinimide {http": "CHEBI:9307", "Co-1": "EFO:0005177", "left ventricular hypertrophy": "EFO:0003896", "Isolated hereditary congenital facial paralysis": "Orphanet:306527", "ILSXISS23/TejJ": "EFO:0002979", "Leymus triticoides": "NCBITaxon:86021", "Ipomoea batatas": "NCBITaxon:4120", "SAPHO syndrome": "EFO:1001164", "autoimmune pancreatitis type 1": "EFO:1000780", "central nervous system development": "GO:0007417", "Acromesomelic dysplasia, Maroteaux type": "Orphanet:40", "Myocardial Ischemia": "EFO:1001375", "ventral": "EFO:0001662", "haloperidol": "CHEBI:5613", "Xylella fastidiosa Temecula1": "NCBITaxon:183190", "Acute kidney injury": "HP:0001919", "plastid": "GO:0009536", "furan": "CHEBI:35559", "Mosaic trisomy 22": "Orphanet:96068", "Klebsiella Infections": "EFO:1001353", "Pyrus pyrifolia": "NCBITaxon:3767", "neutrophil": "CL:0000775", "Autosomal recessive cerebellar ataxia with late-onset spasticity": "Orphanet:352641", "phosphatidylcholine": "CHEBI:49183", "rheumatic fever": "EFO:1001160", "aortitis": "EFO:1000816", "orthostatic intolerance": "EFO:1000645", "hepatitis B virus induced hepatocellular carcinoma": "EFO:0008503", "Idiopathic ventricular fibrillation, not Brugada type": "Orphanet:228140", "Toriello-Lacassie-Droste syndrome": "Orphanet:3339", "Postlingual non-syndromic genetic deafness": "Orphanet:216452", "follicle stimulating hormone": "EFO:0003234", "peripheral arterial disease": "EFO:0004265", "Microcephalic osteodysplastic primordial dwarfism types I and III": "Orphanet:2636", "Brassica rapa": "NCBITaxon:3711", "Skeletal dysplasia - epilepsy - short stature": "Orphanet:1858", "Ovarian Yolk Sac Tumor": "EFO:1000437", "Proteus mirabilis": "NCBITaxon:584", "syncytiotrophoblast cell": "CL:0000525", "Genetic mixed dermis disorder": "Orphanet:183481", "HMEC S1": "EFO:0001189", "Bacillus cereus G9842": "NCBITaxon:405531", "Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency": "Orphanet:1194", "Lactobacillus gasseri": "NCBITaxon:1596", "TP53 mutation status": "EFO:0008382", "Charcot-Marie-Tooth disease type 1D": "Orphanet:101084", "Cortical dysplasia - focal epilepsy syndrome": "Orphanet:163681", "17-Hydroxypregnenolone sulfate {http": "CHEBI:89454", "Medial Tibial Stress Syndrome": "EFO:1001367", "Amelia of lower limb": "Orphanet:294969", "Disorder of pterin metabolism": "Orphanet:309819", "Thrombocytopenia with congenital dyserythropoietic anemia": "Orphanet:67044", "tert-butyl hydroperoxide": "CHEBI:64090", "BisChIP-Seq": "EFO:0008656", "Salla disease": "Orphanet:309334", "estrogen-receptor positive breast cancer": "EFO:1000649", "somatic stem cell": "CL:0000723", "anti-inflammatory drug": "CHEBI:35472", "GM17773 {http": "CLO:0016645", "Methanosarcina mazei": "NCBITaxon:2209", "X-linked sideroblastic anemia with ataxia": "Orphanet:2802", "Ichthyosis follicularis - alopecia - photophobia": "Orphanet:2273", "Graves disease": "EFO:0004237", "beta-nerve growth factor measurement": "EFO:0008035", "myocardial infarction": "EFO:0000612", "volume unit": "UO:0000095", "brain serotonin transporter measurement": "EFO:0004569", "GM17270 {http": "CLO:0013212", "dopamine": "CHEBI:18243", "O-linoleoylcarnitine {http": "CHEBI:73072", "metamyelocyte": "CL:0002192", "lip cancer": "EFO:1001019", "Familial hyperaldosteronism type II": "Orphanet:404", "antibody measurement": "EFO:0004556", "Hyperekplexia - epilepsy": "Orphanet:163985", "Hawkinsinuria": "Orphanet:2118", "wound healing": "GO:0042060", "Polytrichum juniperinum": "NCBITaxon:129213", "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement": "Orphanet:2196", "alive at endpoint": "EFO:0004951", "tetradecanoate {http": "CHEBI:30807", "nucleic acid labeling protocol": "EFO:0003813", "CS57625": "EFO:0000041", "Taeniasis": "EFO:1001433", "Autosomal recessive early-onset inflammatory bowel disease": "Orphanet:238569", "Congenital non-communicating hydrocephalus": "Orphanet:269510", "Palmoplantar keratoderma, Nagashima type": "Orphanet:140966", "pasteurellosis": "EFO:0007424", "low density lipoprotein particle size measurement": "EFO:0008593", "juvenile dermatomyositis": "EFO:0000557", "Genetic syndrome with limb reduction defects": "Orphanet:404574", "MX-1": "EFO:0006457", "Maternal uniparental disomy of chromosome 2": "Orphanet:96179", "Deafness-craniofacial syndrome": "Orphanet:3241", "Bilateral microtia - deafness - cleft palate": "Orphanet:140963", "ATP metabolic process": "GO:0046034", "Rare genetic parathyroid disease and phosphocalcic metabolism disorder": "Orphanet:183634", "caecum": "UBERON:0001153", "circadian sleep/wake cycle, non-REM sleep": "GO:0042748", "Genetic posterior fossa malformation": "Orphanet:269557", "media": "EFO:0000579", "SKNEP1": "EFO:0002337", "genotyping design": "EFO:0001784", "Argininosuccinic aciduria": "Orphanet:23", "Osteoporosis - macrocephaly - blindness - joint hyperlaxity": "Orphanet:2787", "Oculocutaneous albinism type 5": "Orphanet:370091", "Tall stature-intellectual disability-facial dysmorphism syndrome": "Orphanet:404443", "interferon gamma": "EFO:0003024", "Multiple epiphyseal dysplasia, Lowry type": "Orphanet:166016", "antimycin A": "CHEBI:22584", "Disorder of peroxisomal alpha-, beta- and omega-oxidation": "Orphanet:309810", "Alpha-N-acetylgalactosaminidase deficiency type 1": "Orphanet:79279", "virgin": "EFO:0002951", "Paternal uniparental disomy of chromosome 13": "Orphanet:99324", "common carotid intimal medial thickness": "EFO:0004860", "Anal Squamous Cell Carcinoma": "EFO:1000081", "Festuca arundinacea": "NCBITaxon:4606", "interleukin 19 measurement": "EFO:0008180", "pituitary apoplexy": "EFO:1001108", "NCI-H1793": "EFO:0002267", "root nodule": "PO:0003023", "BG03": "EFO:0002960", "slow muscle cell somite 14": "ZFA:0000841", "Fusarium subglutinans": "NCBITaxon:42677", "GM17847 {http": "CLO:0016455", "Asian": "EFO:0003152", "stigma": "PO:0009073", "ticlopidine": "CHEBI:9588", "Tae-Yang": "EFO:0007120", "Coppock-like cataract": "Orphanet:98986", "long poly A RNA": "EFO:0005019", "Musa acuminata": "NCBITaxon:4641", "Listeria meningitis": "EFO:1001021", "HCC1482": "EFO:0006426", "Ly-76 high positive erythrocyte": "CL:0002022", "SNU16": "EFO:0002344", "Hilversum ecotype": "EFO:0006979", "Cronobacter muytjensii": "NCBITaxon:413501", "Terminal limb defects": "Orphanet:294929", "computer": "OBI:0400107", "IGR-37": "EFO:0006597", "Theiler stage 19": "EFO:0004409", "CS57563": "EFO:0000016", "Intervertebral Disc Displacement": "EFO:1001800", "environmental factor": "EFO:0000469", "MNase-seq": "EFO:0003751", "Silver-Russell syndrome due to 7p11.2p13 microduplication": "Orphanet:231137", "Myxococcus xanthus": "NCBITaxon:34", "Weill-Marchesani syndrome": "Orphanet:3449", "CS57606": "EFO:0000031", "cell type": "EFO:0000324", "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement": "Orphanet:31043", "AF16": "EFO:0004063", "Robin sequence - oligodactyly": "Orphanet:3104", "RARseq": "EFO:0008882", "anterior cerebral artery infarction": "EFO:1000807", "non-receptor tyrosine-protein kinase TYK2 measurement": "EFO:0008251", "cellular nitrogen compound metabolic process": "GO:0034641", "Unilateral aplasia of the M\u00c3\u00bcllerian ducts": "Orphanet:180071", "cerebellum cancer": "EFO:1000858", "spondylolisthesis": "EFO:0007493", "Disorder of lipid absorption and transport": "Orphanet:309028", "phosphoethanolamine {http": "CHEBI:36711", "Autosomal recessive limb-girdle muscular dystrophy type 2C": "Orphanet:353", "methylmalonic aciduria cblb type": "EFO:0009074", "embryoid body {http": "UBERON:0014374", "Rothmund-Thomson syndrome type 1": "Orphanet:221008", "mode of inheritance": "HP:0000005", "leg dermatosis": "EFO:1000723", "Central polydactyly of toes, bilateral": "Orphanet:295185", "Streptococcus pneumoniae": "NCBITaxon:1313", "clear cell sarcoma": "EFO:0008498", "Neosartorya fennelliae": "NCBITaxon:41048", "HCC2218": "EFO:0002187", "mucositis": "EFO:1001898", "O-otanoyl-D-carnitine {http": "CHEBI:86051", "Osmerus mordax": "NCBITaxon:8014", "epidermolysis bullosa": "EFO:1000690", "SW480": "EFO:0002083", "beginning of whole plant fruit ripening stage": "PO:0007036", "Septopreoptic holoprosencephaly": "Orphanet:280195", "Myotonic syndrome": "Orphanet:206970", "angiopoietin-1 receptor, soluble measurement": "EFO:0008023", "hematological system disease": "EFO:0005803", "skin mastocytoma": "EFO:1001844", "Generalized peeling skin syndrome": "Orphanet:263543", "Cecum Neuroendocrine Tumor G1": "EFO:1000154", "Bilateral frontal polymicrogyria": "Orphanet:208444", "Chronic diarrhea due to guanylate cyclase 2C overactivity": "Orphanet:314373", "Wolbachia pipientis": "NCBITaxon:955", "porokeratosis": "EFO:1000757", "plant trait": "TO:0000387", "Unknown leukodystrophy": "Orphanet:84096", "colon diverticulum": "EFO:1001296", "toxic epidermal necrolysis": "EFO:0004775", "post-thrombotic syndrome": "EFO:0007452", "segmentation 14-19 somites": "EFO:0001319", "Familial renal amyloidosis due to Apolipoprotein AI variant": "Orphanet:93560", "Hereditary site-specific ovarian cancer syndrome": "Orphanet:213524", "dauer larva": "EFO:0005507", "PBAT": "EFO:0008855", "Bacteroides thetaiotaomicron VPI-5482": "NCBITaxon:226186", "Familial caudal dysgenesis": "Orphanet:1768", "Familial apolipoprotein C-II deficiency": "Orphanet:309020", "chronotype measurement": "EFO:0008328", "501A": "EFO:0006356", "connective tissue type mast cell": "CL:0000484", "immature CD14-positive dermal dendritic cell": "CL:0002527", "ponasterone A": "CHEBI:28135", "Severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome": "Orphanet:397933", "smoking initiation": "EFO:0005670", "Rare constitutional hemolytic anemia due to a red cell membrane anomaly": "Orphanet:98364", "DP-Seq": "EFO:0008718", "enveloping layer": "UBERON:0007383", "zardaverine": "CHEBI:46548", "inbred Mus musculus strain": "EFO:0004005", "shoot": "EFO:0000992", "Endometrial Intraepithelial Neoplasia": "EFO:1000235", "Tall stature - scoliosis - macrodactyly of the great toes": "Orphanet:329191", "Microcephaly - albinism - digital anomalies": "Orphanet:2513", "Congenital pseudoarthrosis of the limbs": "Orphanet:157808", "whole plant fruit ripening stage": "PO:0007010", "Marburg hemorrhagic fever": "EFO:0007358", "ventral mandibular arch": "ZFA:0001273", "Tangier disease": "Orphanet:31150", "Citrus reticulata": "NCBITaxon:85571", "Lactococcus lactis subsp. hordniae": "NCBITaxon:203404", "Disorder of neurotransmitter metabolism and transport": "Orphanet:79169", "fatty acid measurement": "EFO:0005110", "Porencephaly-microcephaly-bilateral congenital cataract syndrome": "Orphanet:306547", "Other immunodeficiency syndrome with predominantly antibody defects": "Orphanet:331244", "(R)-malate(2-) {http": "CHEBI:15588", "Vibrio vulnificus CMCP6": "NCBITaxon:216895", "splenic tuberculosis": "EFO:0007492", "ovarian follicle stage II": "UBERON:2001265", "3-hydroxypropylmercapturic acid measurement": "EFO:0007014", "stomach neoplasm": "EFO:0003897", "lymphoblastoid cell line": "EFO:0005292", "X-linked spondyloepimetaphyseal dysplasia": "Orphanet:93349", "RCHACV": "EFO:0002314", "Genetic disorder of sex development": "Orphanet:325690", "serum lipase activity measurement": "EFO:0005849", "fallopian tube": "UBERON:0003889", "ALG2-CDG": "Orphanet:79326", "mononuclear odontoclast": "CL:0000781", "number of injections": "EFO:0000627", "pulse pressure measurement": "EFO:0005763", "Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma": "EFO:1000591", "institution": "EFO:0001738", "GM12004": "EFO:0001129", "Primary localized amyloidosis": "Orphanet:314709", "Spondyloepiphyseal dysplasia congenita": "Orphanet:94068", "freeze dried specimen": "EFO:0005121", "Sialidosis": "Orphanet:309294", "Pythiosis": "EFO:1001410", "Ichthyosis - hypotrichosis - sclerosing cholangitis": "Orphanet:59303", "CS57620": "EFO:0000037", "function": "BFO:0000034", "Atypical glycine encephalopathy": "Orphanet:289863", "Bdellovibrio bacteriovorus HD100": "NCBITaxon:264462", "euthyroid sick syndrome": "EFO:1000931", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to KIAA0226 deficiency": "Orphanet:404499", "anhidrosis": "EFO:1000670", "Capp-Seq": "EFO:0008672", "Glycogen storage disease due to glycogen synthase deficiency": "Orphanet:308520", "L-cysteinylglycine {http": "CHEBI:4047", "GM17136 {http": "CLO:0015088", "CS57624": "EFO:0000040", "Bangstad syndrome": "Orphanet:1227", "Congenital absence of the eyebrow/eyelashes": "Orphanet:98598", "GM11840 {http": "CLO:0020019", "Male infertility due to sperm motility disorder": "Orphanet:399813", "Polycystic Kidney Disease": "EFO:0008620", "Huntington disease-like syndrome": "Orphanet:158266", "Bordetella bronchiseptica": "NCBITaxon:518", "Autosomal dominant limb-girdle muscular dystrophy type 1A": "Orphanet:266", "taurocholate {http": "CHEBI:36257", "sum of skinfolds": "EFO:0006266", "Childhood absence epilepsy": "Orphanet:64280", "mongolian spot": "EFO:1000736", "Cronobacter turicensis": "NCBITaxon:413502", "Isolated hair shaft abnormality": "Orphanet:79366", "Radial hemimelia": "Orphanet:93321", "Occult macular dystrophy": "Orphanet:247834", "taurolithocholic acid sulfate {http": "CHEBI:17864", "programmed cell death 1 ligand 2 measurement": "EFO:0008268", "Hemophilia B": "Orphanet:98879", "parotid gland": "UBERON:0001831", "J82": "EFO:0002210", "ILSXISS107/TejJ": "EFO:0003005", "Rubinstein-Taybi syndrome due to CREBBP mutations": "Orphanet:353277", "Distal arthrogryposis type 10": "Orphanet:251515", "unit per milliliter": "UO:0000178", "Trichophyton violaceum": "NCBITaxon:34388", "Vitis riparia": "NCBITaxon:96939", "SU-DHL-4": "EFO:0006492", "antidepressant": "CHEBI:35469", "GM17271 {http": "CLO:0013213", "myelophthisic anemia": "EFO:0007388", "CS57816": "EFO:0000128", "COLO704": "EFO:0002139", "Hand-foot syndrome": "EFO:1001893", "Partial duplication of the long arm of chromosome 4": "Orphanet:262860", "Epilepsy syndrome": "Orphanet:166463", "red-green color blindness": "EFO:0005581", "apoplasm": "EFO:0001045", "Staphylococcus saprophyticus": "NCBITaxon:29385", "Harlequin syndrome": "Orphanet:199282", "root tip": "PO:0000025", "mole": "UO:0000013", "Ring chromosome 21": "Orphanet:1445", "phenylephrine": "CHEBI:8093", "Autosomal dominant pure spastic paraplegia": "Orphanet:100980", "Tobacco ringspot virus": "NCBITaxon:12282", "bathocuproine disulfonic acid": "CHEBI:63934", "Streptomyces griseus subsp. griseus NBRC 13350": "NCBITaxon:455632", "epistaxis": "EFO:0003895", "MEC1": "EFO:0002231", "Vibrio cholerae": "NCBITaxon:666", "Reston ebolavirus": "NCBITaxon:186539", "Wildervanck syndrome": "Orphanet:3456", "Acrofacial dysostosis, Palagonia type": "Orphanet:1787", "Lactobacillus": "NCBITaxon:1578", "proventriculus primordium": "FBbt:00005550", "mucinuos carcinoma": "EFO:1000387", "Rare genetic tremor disorder": "Orphanet:307061", "left inferior lateral ventricle volume measurement": "EFO:0006793", "Complete androgen insensitivity syndrome": "Orphanet:99429", "Large congenital melanocytic nevus": "Orphanet:626", "noma": "EFO:1001063", "Autosomal dominant spastic paraplegia type 12": "Orphanet:100993", "cerebrospinal fluid clusterin measurement": "EFO:0007657", "polar solvent role": "CHEBI:48354", "Staphylococcus lugdunensis": "NCBITaxon:28035", "Ring chromosome 11": "Orphanet:96175", "Huntington disease-like 2": "Orphanet:98934", "Familial adenomatous polyposis": "Orphanet:733", "Peripheral hypothyroidism": "Orphanet:226310", "X-linked intellectual disability, Sutherland-Haan type": "Orphanet:93950", "Distal monosomy 9p": "Orphanet:1642", "DAP-seq": "EFO:0008705", "Gastric Squamous Cell Carcinoma": "EFO:1000278", "sex ratio": "EFO:0004820", "Atrioventricular canal defect": "HP:0006695", "Fu97": "EFO:0002054", "erythroplasia": "EFO:1001786", "Corneal dystrophy - perceptive deafness": "Orphanet:1490", "lateral epicondylitis": "EFO:1001896", "GM17774 {http": "CLO:0016641", "Severe congenital nemaline myopathy": "Orphanet:171430", "ribothymidine {http": "CHEBI:45996", "Deficiency in anterior pituitary function-variable immunodeficiency syndrome": "Orphanet:293978", "cutaneous fibrous histiocytoma": "EFO:1000885", "cadmium dichloride": "CHEBI:35456", "Focal dermal hypoplasia": "Orphanet:2092", "Genetic subcutaneous tissue disorder": "Orphanet:183484", "Lissencephaly with cerebellar hypoplasia type F": "Orphanet:100016", "anti-neutrophil antibody associated vasculitis": "EFO:0004826", "cleavage 64-cell": "EFO:0001288", "CS57648": "EFO:0000052", "Immunodeficiency predominantly affecting antibody production": "Orphanet:101977", "adrenal rest tumor": "EFO:1000798", "cholesteatoma": "EFO:1000675", "Partial deletion of the long arm of chromosome 7": "Orphanet:262056", "trimethyltin": "CHEBI:63948", "Paternal uniparental disomy of chromosome 7": "Orphanet:96192", "BSPP": "EFO:0008667", "heart component": "EFO:0001955", "Eucalyptus grandis x Eucalyptus urophylla": "NCBITaxon:192399", "Hearing abnormality": "HP:0000364", "Hs 294T": "EFO:0006585", "abdominal aorta": "UBERON:0001516", "Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency": "Orphanet:324262", "job-related exhaustion measurement": "EFO:0007881", "Mirror polydactyly - vertebral segmentation - limbs defects": "Orphanet:3004", "poisoning": "EFO:0008546", "A204.1": "EFO:0005702", "Cuscuta pentagona": "NCBITaxon:112407", "nongranular leukocyte": "CL:0002087", "Meckel's diverticulum": "EFO:1001036", "response to dendritic cell-based immunotherapy": "EFO:0007880", "GM17769 {http": "CLO:0016648", "indole-3-acetic acid": "CHEBI:16411", "Candidatus Blochmannia floridanus": "NCBITaxon:203907", "blood pressure": "EFO:0004325", "C57BL/6J": "EFO:0000606", "X-linked calvarial hyperostosis": "Orphanet:391327", "pentamidine": "CHEBI:45081", "Autosomal recessive spastic paraplegia type 28": "Orphanet:101008", "vaspin measurement": "EFO:0004915", "Pyruvate carboxylase deficiency, severe neonatal type": "Orphanet:353314", "glanders": "EFO:0007286", "Severe early-onset axonal neuropathy due to MFN2 deficiency": "Orphanet:90118", "methodological variation design": "EFO:0004669", "embryonic central brain pars intercerebralis": "FBbt:00005667", "GM06993": "EFO:0001108", "IMP {http": "CHEBI:17202", "Silver-Russell syndrome due to 11p15 microduplication": "Orphanet:231144", "Autosomal dominant congenital benign spinal muscular atrophy": "Orphanet:1216", "Endometrial Polyp": "EFO:1000237", "Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis": "Orphanet:93220", "HT55": "EFO:0006444", "Hemochromatosis type 3": "Orphanet:225123", "ZR751": "EFO:0001262", "colon adenocarcinoma": "EFO:1001949", "SMA": "EFO:0008929", "vitamin K-dependent protein C measurement": "EFO:0008318", "C33A": "EFO:0002120", "Craniomicromelic syndrome": "Orphanet:1524", "N-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-2-(2,6-dimethoxyphenoxy)ethanamine": "CHEBI:64098", "bone geometry": "EFO:0004513", "presomitic mesoderm": "UBERON:0003059", "639V": "EFO:0002097", "Seizures - intellectual disability due to hydroxylysinuria": "Orphanet:79156", "Gallbladder Adenoma": "EFO:1000263", "cell cycle process": "GO:0022402", "monocyte count": "EFO:0005091", "polyethylene glycol": "CHEBI:46793", "Cervical Glandular Intraepithelial Neoplasia": "EFO:1000165", "Dengue virus 3": "NCBITaxon:11069", "NSCR": "EFO:0008832", "acute myelomonocytic leukemia": "EFO:0000223", "mouse embryonic stem cell": "EFO:0004038", "Partial duplication of chromosome 7": "Orphanet:262633", "CHART": "EFO:0008681", "Bathing suit ichthyosis": "Orphanet:100976", "lung endoderm": "EFO:0002578", "margarate {http": "CHEBI:32366", "hyRAD": "EFO:0008772", "Dermotrichic syndrome": "Orphanet:99688", "Glutaric acidemia {http": "HP:0003530", "Osteogenesis imperfecta type 2": "Orphanet:216804", "cardiac hypertrophy": "EFO:0002503", "Periodontal Pocket": "EFO:1001393", "Autosomal recessive infantile hypercalcemia": "Orphanet:300547", "Immunodeficiency due to selective anti-polysaccharide antibody deficiency": "Orphanet:70593", "Pallister-Hall syndrome": "Orphanet:672", "adiposis dolorosa": "EFO:1000667", "EMG abnormality {http": "HP:0003457", "17p11.2 microduplication syndrome": "Orphanet:1713", "Podoviridae": "NCBITaxon:10744", "gastritis": "EFO:0000217", "carboplatin": "CHEBI:31355", "ILSXISS7/TejJ": "EFO:0002973", "British": "EFO:0003155", "retinopathy": "EFO:0003839", "skeletal system": "UBERON:0001434", "seminal vesicle": "UBERON:0000998", "lipoprotein-associated phospholipase A(2) measurement": "EFO:0004746", "Gonadal dysgenesis of gynecological interest": "Orphanet:98074", "Multiple acyl-CoA dehydrogenase deficiency": "Orphanet:26791", "primary root tip {http": "PO:0000026", "protein modification process": "GO:0036211", "chronic myelomonocytic leukemia": "EFO:1001779", "soil environment {http": "EO:0007049", "Imperforate oropharynx - costo vetebral anomalies": "Orphanet:2759", "hypoxanthine {http": "CHEBI:17368", "Pick disease": "EFO:0003096", "Orofaciodigital syndrome type 10": "Orphanet:2756", "EB2": "EFO:0002173", "SSRI use measurement": "EFO:0007011", "intracellular": "GO:0005622", "lupus nephritis": "EFO:0005761", "DSB-seq": "EFO:0008724", "Streptococcus mitis": "NCBITaxon:28037", "brain aneurysm": "EFO:0003870", "allyl alcohol": "CHEBI:16605", "seborrheic dermatitis": "EFO:1000764", "nanoliter": "UO:0000102", "GM11882": "EFO:0001123", "Distal trisomy 6p": "Orphanet:1745", "fat body mass": "EFO:0005409", "Neonatal severe primary hyperparathyroidism": "Orphanet:417", "pituitary gland": "UBERON:0000007", "carotid artery mean blood pressure measurement": "EFO:0007723", "pelvic girdle": "ZFA:0000565", "abdominal abscess": "EFO:1001753", "Klippel-Tr\u00c3\u00a9naunay syndrome": "Orphanet:90308", "Larsen-like osseous dysplasia - short stature": "Orphanet:2370", "monocyte-derived intermediate cell": "EFO:0002665", "GM14406 {http": "CLO:0031228", "Drosophila simulans HW09": "EFO:0004029", "Branchioma": "EFO:1001277", "dental caries": "EFO:0003819", "dual specificity mitogen-activated protein kinase kinase 2 measurement": "EFO:0008112", "Genetic optic atrophy": "Orphanet:103", "Legionnaires' disease": "EFO:0007343", "Familial hypocalciuric hypercalcemia type 1": "Orphanet:93372", "Takayasu arteritis": "EFO:1001857", "Heritable pulmonary arterial hypertension": "Orphanet:275777", "response to combination chemotherapy": "EFO:0007965", "N-acetyl-L-threonine {http": "CHEBI:45826", "Lactobacillus paralimentarius": "NCBITaxon:83526", "Severe Canavan disease": "Orphanet:314911", "Glycogen storage disease due to acid maltase deficiency, adult onset": "Orphanet:308604", "T2 tumor stage": "EFO:0004939", "GM17141 {http": "CLO:0013939", "Metanephric Adenoma": "EFO:1000373", "Familial partial lipodystrophy": "Orphanet:98306", "Treponema denticola": "NCBITaxon:158", "Isolated asymptomatic elevation of creatine phosphokinase": "Orphanet:206599", "bezafibrate": "CHEBI:47612", "pulmonary fibrosis and/or bone marrow failure, telomere-related, 1": "EFO:1001501", "ND06449 {http": "CLO:0018566", "antiemetic": "CHEBI:50919", "skin sarcoidosis": "EFO:1000767", "Arabidopsis thaliana": "NCBITaxon:3702", "cancer site": "EFO:0000312", "kilogram": "UO:0000009", "Peripheral dysostosis": "Orphanet:1795", "menarche": "EFO:0003930", "aortic stenosis": "EFO:0000266", "chin morphology measurement": "EFO:0007842", "SJSA1": "EFO:0002330", "bone": "UBERON:0001474", "Spinocerebellar ataxia type 28": "Orphanet:101109", "transferrin measurement": "EFO:0006341", "Neisseria gonorrhoeae": "NCBITaxon:485", "acidophil adenoma": "EFO:1000791", "Phosphoenolpyruvate carboxykinase 1 deficiency": "Orphanet:79316", "Bone dysplasia, Azouz type": "Orphanet:1844", "dorsal apodeme specific anlage": "EFO:0000413", "Tungiasis": "EFO:1001445", "primary segmental branch primordium": "FBbt:00017011", "Rosa lucieae": "NCBITaxon:74648", "NHEK": "EFO:0002799", "Boomerang dysplasia": "Orphanet:1263", "Neospora caninum": "NCBITaxon:29176", "Adult-onset citrullinemia type I": "Orphanet:247573", "dendritic epidermal T cell": "CL:0000916", "shoulder": "UBERON:0001467", "Cervical hypertrichosis - peripheral neuropathy": "Orphanet:2218", "Progressive bifocal chorioretinal atrophy": "Orphanet:75373", "organization role": "EFO:0002012", "Pyruvate metabolism disorder": "Orphanet:254746", "BJ": "EFO:0002779", "Spondylo-ocular syndrome": "Orphanet:85194", "ZHBTc4-mESC": "EFO:0005914", "6alpha-methylprednisolone": "CHEBI:6888", "Neisseria elongata": "NCBITaxon:495", "Genetic peripheral neuropathy": "Orphanet:98497", "RAS-associated autoimmune leukoproliferative disease": "Orphanet:268114", "Combined oxidative phosphorylation defect type 26": "EFO:0009036", "Kartagener Syndrome": "EFO:1001352", "Microcephaly - cervical spine fusion anomalies": "Orphanet:2522", "SC": "EFO:0007029", "vascular brain injury measurement": "EFO:0006800", "bartonellosis": "EFO:0007166", "BeWo": "EFO:0002050", "pulmonary trunk": "UBERON:0002333", "Congenital lethal erythroderma": "Orphanet:1954", "Craniofacial dysplasia-osteopenia syndrome": "Orphanet:314555", "endocrine neoplasm": "EFO:0003769", "embryonic ganglion mother cell": "FBbt:00001433", "glycocholate {http": "CHEBI:29746", "Orofaciodigital syndrome type 1": "Orphanet:2750", "CD103-positive dendritic cell": "CL:0002461", "Ramsay-Hunt syndrome": "Orphanet:3020", "Splenogonadal fusion - limb defects - micrognathia": "Orphanet:2063", "erythroleukemia cell": "BTO:0000426", "Isolated anencephaly/exencephaly": "Orphanet:1048", "biological replicate": "EFO:0002091", "familial amyotrophic lateral sclerosis": "EFO:0001356", "Unilateral retinoblastoma": "Orphanet:357034", "ATC Code D Dermatologicals": "EFO:0005637", "Pan paniscus": "NCBITaxon:9597", "Congenital and infantile nephrotic syndrome": "Orphanet:97556", "4-vinylphenol sulfate {http": "CHEBI:82931", "Brassica oleracea": "NCBITaxon:3712", "Hereditary episodic ataxia": "Orphanet:211062", "dorsal epidermis primordium": "UBERON:6005526", "anterior ischemic optic neuropathy": "EFO:1000809", "EST sequencing": "EFO:0003754", "Odontoleukodystrophy": "Orphanet:77295", "Rare genetic odontologic disease": "Orphanet:77830", "CS57835": "EFO:0000138", "calcium measurement": "EFO:0004838", "Crigler-Najjar syndrome type 2": "Orphanet:79235", "46,XX disorder of sex development - skeletal anomalies": "Orphanet:2975", "Mediastinal Neuroblastoma": "EFO:1000367", "HUES64-derived CD184+": "EFO:0007090", "vitamin K measurement": "EFO:0004618", "Kidney Angiomyolipoma": "EFO:1000312", "DR1567": "EFO:0004085", "T-B+ severe combined immunodeficiency due to JAK3 deficiency": "Orphanet:35078", "X-linked distal hereditary motor neuropathy": "Orphanet:404538", "SMDB": "EFO:0008932", "Adolescent-onset epilepsy syndrome": "Orphanet:98260", "Cannabis use": "EFO:0007585", "anterior lateral line placode": "UBERON:2001316", "GM13995 {http": "CLO:0033909", "Familial vascular leukoencephalopathy": "Orphanet:36383", "CS57705": "EFO:0000066", "low density lipoprotein cholesterol measurement": "EFO:0004611", "biotic plant treatment": "EO:0007357", "median fin skeleton": "UBERON:4000170", "Yu-Zhi constitution type": "EFO:0007638", "neural arch": "UBERON:0003861", "renal glycosuria": "EFO:1001151", "Papillary Meningioma": "EFO:1000449", "Neisseria flavescens": "NCBITaxon:484", "mesoblastic nephroma": "EFO:0007365", "Genetic respiratory or mediastinal malformation": "Orphanet:183554", "Bacteroides fragilis YCH46": "NCBITaxon:295405", "pancreatitis": "EFO:0000278", "ME-Scan-SVA": "EFO:0008802", "Grange syndrome": "Orphanet:79094", "Ataxia-oculomotor apraxia type 4": "EFO:0009016", "array control hybridization quality": "EFO:0005437", "dissociation protocol": "EFO:0009088", "CS57603": "EFO:0000030", "Permanent congenital hypothyroidism": "Orphanet:226292", "inflammation (MPATH)": "MPATH:212", "cap analysis gene expression": "EFO:0004181", "Familial gestational hyperthyroidism": "Orphanet:99819", "Pseudohypoaldosteronism type 2": "Orphanet:757", "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis": "Orphanet:306516", "leaf mesophyll {http": "PO:0005645", "Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency": "Orphanet:319600", "segregating inbred strain": "EFO:0004009", "total cholesterol change measurement": "EFO:0007806", "537 MEL": "EFO:0006357", "GM17240 {http": "CLO:0014410", "response to triamcinolone acetonide": "EFO:0006954", "CCD-18Co cell": "BTO:0004059", "Neurofibromatosis type 1": "Orphanet:636", "CEM/C1": "EFO:0001667", "Fibular aplasia - complex brachydactyly": "Orphanet:2639", "Autosomal dominant nocturnal frontal lobe epilepsy": "Orphanet:98784", "psoriatic arthritis": "EFO:0003778", "topoisomerase II inhibitor": "CHEBI:50750", "Ichthyosis - oral and digital anomalies": "Orphanet:2272", "Autosomal dominant spastic ataxia": "Orphanet:316235", "Cervus elaphus": "NCBITaxon:9860", "eosinophil count": "EFO:0004842", "GM17205 {http": "CLO:0013834", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome": "Orphanet:404481", "ATC Code C Cardiovascular system": "EFO:0005636", "Erythrokeratodermia variabilis": "Orphanet:317", "malnutrition": "EFO:0008572", "Silver-Russell syndrome due to imprinting defect of 11p15": "Orphanet:231140", "Immunodeficiency by defective expression of HLA class 1": "Orphanet:34592", "GM14521 {http": "CLO:0031612", "electrodermal activity measurement": "EFO:0006866", "Trichophyton terrestre": "NCBITaxon:81845", "3\u00e2\u0080\u0099-end-seq": "EFO:0008641", "Candida parapsilosis": "NCBITaxon:5480", "iCLIP": "EFO:0008774", "Benign familial infantile epilepsy": "Orphanet:306", "Distal 17p13.3 microdeletion syndrome": "Orphanet:261257", "X-Linked Combined Immunodeficiency Diseases": "EFO:1001451", "Congenital myopathy with excess of thin filaments": "Orphanet:98904", "Aeromonas hydrophila infection": "EFO:0000776", "Tetrahymena thermophila": "NCBITaxon:5911", "blackwater fever": "EFO:0007172", "nucleobase-containing small molecule metabolic process": "GO:0055086", "kinetin": "CHEBI:27407", "Achondrogenesis type 1B": "Orphanet:93298", "QRS complex": "EFO:0005054", "Hypodontia - dysplasia of nails": "Orphanet:2228", "Congenital pseudoarthrosis of the femur": "Orphanet:295020", "micromole per liter": "EFO:0002901", "Atypical hemolytic-uremic syndrome with H factor anomaly": "Orphanet:93579", "Progressive non-fluent aphasia": "Orphanet:100070", "naive B cell": "CL:0000788", "mouse embryo stage": "EFO:0005857", "Microcephaly - lymphedema - chorioretinopathy": "Orphanet:2526", "area unit": "UO:0000047", "U-698-M": "EFO:0006768", "peak insulin response measurement": "EFO:0008000", "Exiguobacterium sibiricum 255-15": "NCBITaxon:262543", "L3 larva": "EFO:0002720", "SW837": "EFO:0002372", "chloronema {http": "PO:0030004", "A673": "EFO:0002106", "intercostal muscle": "UBERON:0001111", "purine ribonucleoside triphosphate biosynthetic process": "GO:0009206", "23132/87": "EFO:0006528", "extracellular matrix": "GO:0031012", "sepsis": "HP:0100806", "IgD plasmablast": "CL:0000949", "16q24.3 microdeletion syndrome": "Orphanet:261250", "LP.05 five leaves visible stage": "PO:0007065", "Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells": "Orphanet:83620", "cholesterol ester": "CHEBI:17002", "mouth disease": "EFO:1001047", "YEPD": "EFO:0007025", "Congenital muscular dystrophy with intellectual disability": "Orphanet:370968", "Primary Melanocytic Lesion of Meninges": "EFO:1000493", "presumptive hindbrain": "UBERON:0007277", "Ligneous conjunctivitis": "Orphanet:97231", "HRE": "EFO:0002794", "apical meristem {http": "PO:0020144", "Oystese ecotype": "EFO:0006973", "Non-Cutaneous Melanoma": "EFO:1000397", "Blastocystis hominis infectious disease": "EFO:0007173", "Familial or sporadic hemiplegic migraine": "Orphanet:569", "chlorpropamide": "CHEBI:3650", "Tetrasomy 18p": "Orphanet:3307", "spotted protein reporter": "EFO:0005077", "Meesmann corneal dystrophy": "Orphanet:98954", "Scalp-ear-nipple syndrome": "Orphanet:2036", "vein graft stenosis": "EFO:0007051", "1-[(4Z,7Z,10Z,13Z,16Z)-docosapentaenoyl]-sn-glycero-3-phosphocholine {http": "CHEBI:74348", "DT40": "EFO:0006274", "visual anlage": "UBERON:6005434", "interleukin 18 (Homo sapiens)": "EFO:0004580", "black piedra": "EFO:0007171", "lactate measurement": "EFO:0007745", "underweight body mass index status": "EFO:0005936", "Glycogen storage disease due to liver glycogen phosphorylase deficiency": "Orphanet:369", "post-traumatic stress disorder": "EFO:0001358", "innate behavior design": "EFO:0001749", "Human adenovirus 40": "NCBITaxon:28284", "Supravalvular aortic stenosis": "Orphanet:3193", "Autosomal recessive ataxia due to ubiquinone deficiency": "Orphanet:139485", "tumor stage": "EFO:0004925", "style {http": "PO:0009074", "Spastic ataxia - corneal dystrophy": "Orphanet:2572", "ChIP": "EFO:0004176", "meristematic apical cell {http": "PO:0030007", "Von Willebrand disease": "Orphanet:903", "xylonate {http": "CHEBI:27345", "GM10832 {http": "CLO:0023794", "Secondary glaucoma due to a proliferation and differentiation anomaly": "Orphanet:98637", "Niemann-Pick disease type C, severe early infantile neurologic onset": "Orphanet:216975", "Saccharomyces mikatae IFO 1815": "NCBITaxon:226126", "Methicillin-Resistant Staphylococcus Aureus Pneumonia": "EFO:0008556", "Fibular aplasia - ectrodactyly": "Orphanet:1118", "response to metformin": "GO:1901558", "antiatherogenic agent": "CHEBI:50855", "Hirsutism-skeletal dysplasia-intellectual disability syndrome": "Orphanet:2156", "preBCR-negative large pre-B-II cell": "CL:0000953", "cervical neck region": "EFO:0001408", "hippocampal neuron": "CL:0002608", "Papio anubis": "NCBITaxon:9555", "1-monolinolein {http": "CHEBI:75568", "Congenital knee dislocation": "Orphanet:295034", "Teebi-Shaltout syndrome": "Orphanet:3291", "HIV wasting syndrome": "EFO:0007312", "midbrain tectum": "UBERON:0002314", "Autosomal recessive myogenic arthrogryposis multiplex congenita": "Orphanet:319332", "Prune belly syndrome": "Orphanet:2970", "Genetic respiratory malformation": "Orphanet:183622", "SC-1": "EFO:0006481", "Erythropoietic uroporphyria associated with myeloid malignancy": "Orphanet:280379", "Commotio Cordis": "EFO:1001781", "primary hyperparathyroidism": "EFO:0008519", "mid rosette growth stage": "PO:0007068", "GM17128 {http": "CLO:0015128", "Lethal hemolytic anemia - genital anomalies": "Orphanet:1046", "Saccharomyces cerevisiae": "NCBITaxon:4932", "Orofaciodigital syndrome type 3": "Orphanet:2752", "total RNA": "EFO:0004964", "pseudorabies": "EFO:0007457", "somatic cell": "CL:0002371", "Erwinia chrysanthemi": "NCBITaxon:556", "Legius syndrome": "Orphanet:137605", "Small Intestinal Tubulovillous Adenoma": "EFO:1000539", "mating type": "EFO:0001268", "BruDRB-seq": "EFO:0008663", "Dysmorphism - cleft palate - loose skin": "Orphanet:1779", "mucosa-associated lymphoid tissue macrophage": "CL:0000884", "Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome": "Orphanet:369979", "Pectobacterium atrosepticum": "NCBITaxon:29471", "Primary lipodystrophy": "Orphanet:90970", "viral human hepatitis infection": "EFO:0004196", "methamphetamine-induced psychosis": "EFO:0005242", "Short stature - webbed neck - heart disease": "Orphanet:2865", "normalization testing design": "EFO:0001771", "Schizencephaly": "Orphanet:799", "Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome": "Orphanet:293864", "assay by high throughput sequencer": "EFO:0002697", "chronic rhinosinusitis": "EFO:1000024", "puromycin": "CHEBI:17939", "SW1783": "EFO:0002364", "3-methylglutaconic aciduria type 3": "Orphanet:67047", "(7Z,10Z,13Z,16Z)-docosatetraenoate {http": "CHEBI:77225", "A4/Fuk": "EFO:0006533", "2q31.1 microdeletion syndrome": "Orphanet:251014", "T4b tumor stage": "EFO:0004946", "eumycotic mycetoma": "EFO:0007265", "anthracosilicosis": "EFO:1000813", "response to opiate": "GO:0014072", "DNA": "CHEBI:16991", "trans-4-hydroxy-L-proline {http": "CHEBI:18095", "Fc-epsilon RIalpha-high basophil progenitor cell": "CL:0002030", "distant metastasis free survival": "EFO:0000412", "Non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations": "Orphanet:178025", "tumor necrosis factor-alpha": "EFO:0003271", "pure tone hearing measurement": "EFO:0007617", "esophagus": "UBERON:0001043", "presumptive pronephric mesoderm": "UBERON:0007297", "Hypertrichotic osteochondrodysplasia, Cantu type": "Orphanet:1517", "response to transplant": "EFO:0007043", "Epiphyses, Slipped": "EFO:1001317", "vagus nerve": "UBERON:0001759", "muscle cell derived cell line": "EFO:0005734", "GM12005": "EFO:0001130", "Brachydactylous dwarfism, Mseleni type": "Orphanet:2619", "IgM memory B cell": "CL:0000971", "Young adult-onset distal hereditary motor neuropathy": "Orphanet:314485", "Leukoencephalopathy - ataxia - hypodontia - hypomyelination": "Orphanet:137639", "KID syndrome": "Orphanet:477", "Maternal uniparental disomy of chromosome 16": "Orphanet:96185", "Charcot-Marie-Tooth disease type 4A": "Orphanet:99948", "vulvar leiomyosarcoma": "EFO:1001975", "response to mTOR inhibitor": "EFO:0005417", "Hyperplastic Polyp": "EFO:1000299", "Spinal muscular atrophy with respiratory distress type 1": "Orphanet:98920", "Alexander disease type II": "Orphanet:363722", "Common mesentery": "Orphanet:620", "infant expressive language ability": "EFO:0006316", "urate salt {http": "CHEBI:46819", "response to antidepressant": "GO:0036276", "Pectobacterium carotovorum infection": "EFO:0000781", "rasopathy": "EFO:1001502", "CAL-12T": "EFO:0006547", "geometric modifier": "EFO:0001648", "advanced glycation end-product measurement": "EFO:0007819", "CS57717": "EFO:0000073", "GM17779 {http": "CLO:0016635", "Joubert syndrome with renal defect": "Orphanet:220497", "protein transport": "GO:0015031", "X12063 measurement": "EFO:0006957", "Spinocerebellar ataxia type 29": "Orphanet:208513", "oropharynx": "UBERON:0001729", "Ring chromosome 7": "Orphanet:1449", "adrenal gland neoplasm": "EFO:0003850", "Lactobacillus pontis": "NCBITaxon:35787", "transposition": "EFO:0004021", "Delphinapterus leucas": "NCBITaxon:9749", "Superior Vena Cava Syndrome": "EFO:1001855", "Congenital microcoria": "Orphanet:566", "nucleic acid extraction protocol": "EFO:0002944", "Herpesviridae infectious disease": "EFO:0007309", "Cockayne syndrome type 3": "Orphanet:90324", "HCC2185": "EFO:0001178", "Childhood-onset nemaline myopathy": "Orphanet:171439", "sleep apnea measurement during REM sleep": "EFO:0008455", "GM17733 {http": "CLO:0016995", "Trisomy 8q": "Orphanet:1752", "smooth surface dental caries": "EFO:0006339", "response to antimicrotubule agent": "EFO:0005260", "Epstein-Barr virus-related Burkitts lymphoma": "EFO:1001954", "Acrocephalosyndactyly": "Orphanet:946", "Dysmetria {http": "HP:0001310", "Hyperprolinemia type 1": "Orphanet:419", "glucagon measurement": "EFO:0008463", "PAS-Seq": "EFO:0008850", "large pre-B-II cell": "CL:0000957", "Eyebrow/eyelashes pigmentation anomaly": "Orphanet:98601", "H syndrome": "Orphanet:168569", "Emery-Nelson syndrome": "Orphanet:1927", "neoplasm of immature B and T cells": "EFO:0002425", "Xanthinuria type II": "Orphanet:93602", "Theobroma cacao": "NCBITaxon:3641", "food addiction measurement": "EFO:0007830", "unswitched memory B cell": "CL:0000970", "pericardial adipose tissue measurement": "EFO:0007890", "thioproline {http": "CHEBI:64564", "CHGB cleavage product measurement": "EFO:0007910", "dorsal skin": "EFO:0001907", "immune system disease": "EFO:0000540", "Absent tibia - polydactyly": "Orphanet:988", "Uk-1": "EFO:0005161", "5,6-dihydrothymine {http": "CHEBI:27468", "3-phosphoglycerate(2-) {http": "CHEBI:88005", "Blepharospasm - oromandibular dystonia": "Orphanet:93964", "IGROV-1": "EFO:0005385", "leukopenia": "EFO:0004233", "well-differentiated liposarcoma": "EFO:0000736", "autosomal dominant compelling helio-ophthalmic outburst syndrome": "EFO:0007887", "Monostotic fibrous dysplasia": "Orphanet:93277", "Progressive supranuclear palsy - pure akinesia with gait freezing": "Orphanet:240094", "cellular component organization": "GO:0016043", "Primary parathyroids hyperplasia": "Orphanet:99878", "Duodenal atresia": "Orphanet:1203", "loess transformation": "OBI:0200071", "Primary renal tubular acidosis": "Orphanet:314822", "Treponema pallidum": "NCBITaxon:160", "Oculocerebrocutaneous syndrome": "Orphanet:1647", "Monomelic amyotrophy": "EFO:1001989", "GM17229 {http": "CLO:0014362", "gamma chain deficiency": "EFO:0005555", "WSU-FSCCL": "EFO:0006776", "in-cell SHAPE-Seq": "EFO:0008779", "smoking behavior": "EFO:0004318", "pneumonic pasteurellosis": "EFO:0007449", "Weaver syndrome": "Orphanet:3447", "renal cell carcinoma": "EFO:0000681", "thymus primordium": "UBERON:0005562", "MEGDEL syndrome": "Orphanet:352328", "Coprinopsis cinerea": "NCBITaxon:5346", "Rattus norvegicus": "NCBITaxon:10116", "Cardiomyopathy - cataract - hip spine disease": "Orphanet:1345", "NCI-H820": "EFO:0003125", "X-linked intellectual disability - spastic quadriparesis": "Orphanet:163982", "periodontal measurement": "EFO:0007780", "HCC515": "EFO:0003135", "CS57671": "EFO:0000059", "ciguatera poisoning": "EFO:1001291", "sequencer": "EFO:0003739", "Onthophagus taurus": "NCBITaxon:166361", "heart": "UBERON:0000948", "Kunitz-type protease inhibitor 2 measurement": "EFO:0008200", "IPC-298": "EFO:0006447", "aspirin use measurement": "EFO:0007013", "reproductive system": "UBERON:0000990", "postburn hypertrophic scarring severity measurement": "EFO:0007747", "Short rib-polydactyly syndrome, Verma-Naumoff type": "Orphanet:93271", "Humeral agenesis/hypoplasia, bilateral": "Orphanet:295063", "Glycogen storage disease due to aldolase A deficiency": "Orphanet:57", "Fusarium anthophilum": "NCBITaxon:48485", "artesunate": "CHEBI:63918", "airway imaging measurement": "EFO:0007627", "zebrafish component": "EFO:0003331", "HIV-associated nephropathy": "EFO:0007313", "T3c tumor stage": "EFO:0004943", "ACH-3P": "EFO:0006269", "bile": "UBERON:0001970", "TaDa": "EFO:0008959", "Boran cattle": "EFO:0005183", "economic and social preference": "EFO:0004827", "Familial isolated clinodactyly of fingers": "Orphanet:295014", "allopurinol riboside {http": "CHEBI:74074", "ossifying fibroma": "EFO:0007412", "triglyceride measurement": "EFO:0004530", "Lactococcus lactis subsp. lactis": "NCBITaxon:1360", "blood zinc measurement": "EFO:0007584", "Fibrous dysplasia of bone": "Orphanet:249", "Bacteroides fragilis NCTC 9343": "NCBITaxon:272559", "Congenital dyserythropoietic anemia type IV": "Orphanet:293825", "benign": "EFO:0002751", "keratinocyte": "CL:0000312", "JJ012": "EFO:0006604", "Non-Functioning Adrenal Cortex Adenoma": "EFO:1000399", "Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy": "Orphanet:97555", "Interauricular communication": "Orphanet:1478", "GM17793 {http": "CLO:0016678", "iron deficiency anemia": "HP:0001891", "Neurodegeneration with brain iron accumulation due to C19orf12 mutation": "Orphanet:289560", "seed imbibition stage": "PO:0007022", "slow muscle cell somite 1": "ZFA:0000963", "Autosomal dominant limb-girdle muscular dystrophy type 1H": "Orphanet:238755", "Autosomal recessive cerebelloparenchymal disorder type 3": "Orphanet:1170", "piperazine": "CHEBI:28568", "response to cold medicine": "EFO:0006997", "Undifferentiated Ovarian Carcinoma": "EFO:1000605", "Meningioangiomatosis": "EFO:1000371", "Familial advanced sleep-phase syndrome": "Orphanet:164736", "Myoclonic epilepsy in non-progressive encephalopathies": "Orphanet:86913", "Abnormal cortical gyration {http": "HP:0002536", "Midline defect of mandible": "HP:0010753", "biofilm": "BTO:0002690", "fruit development stage {http": "PO:0001002", "death-associated protein kinase 2 measurement": "EFO:0008107", "Megalencephaly-capillary malformation-polymicrogyria syndrome": "Orphanet:60040", "4-nitrotoluene": "CHEBI:35227", "pleomorphic breast carcinoma": "EFO:1000047", "Tuberculosis, Bovine": "EFO:1001441", "necrotizing enterocolitis": "EFO:0003928", "Japanese encephalitis": "EFO:0007332", "eye-antennal disc": "FBbt:00001766", "GM15590 {http": "CLO:0028103", "Ehlers-Danlos syndrome, arthrochalasic type": "Orphanet:1899", "skin appendage carcinoma": "EFO:1001183", "1-oleoyl-2-linoleoyl-glycerol (18": "CHEBI:75450", "4-hydroxycoumarin {http": "CHEBI:40070", "Van den Bosch syndrome": "Orphanet:3417", "Populus alba": "NCBITaxon:43335", "Glycogen storage disease": "Orphanet:79201", "Sequence Read Format (SRF)": "EFO:0004154", "Crush Syndrome": "EFO:1001299", "Y79": "EFO:0002392", "telencephalon neural crest": "UBERON:0003850", "overall survival": "EFO:0000638", "Escherichia coli BL21": "NCBITaxon:511693", "response to docetaxel": "GO:1902519", "Mseek": "EFO:0008823", "EFM-192B": "EFO:0006569", "Seoul virus": "NCBITaxon:11608", "X-linked intellectual disability, Golabi-Ito-Hall type": "Orphanet:93947", "Generalized basaloid follicular hamartoma syndrome": "Orphanet:168632", "polyamide": "CHEBI:51953", "presumptive telencephalon": "UBERON:0014371", "Neuroacanthocytosis": "Orphanet:263440", "amoxicillin": "CHEBI:2676", "Benign Conjunctival Neoplasm": "EFO:1000110", "Breslow thickness": "EFO:0004955", "AG06237 {http": "CLO:0035254", "Lotus japonicus": "NCBITaxon:34305", "epithelium": "UBERON:0000483", "Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis": "Orphanet:352662", "Xiphophorus": "NCBITaxon:8082", "Nail-patella-like renal disease": "Orphanet:2613", "X-linked intellectual disability, Schutz type": "Orphanet:3062", "familial apolipoprotein B hypobetalipoproteinemia": "EFO:1001789", "major depressive episode": "EFO:0007634", "parotid disease": "EFO:0007422", "embryonic day 9.5": "EFO:0007641", "paraneoplastic polyneuropathy": "EFO:1001085", "Sedum alfredii": "NCBITaxon:439688", "Hodgkins lymphoma, mixed cellularity": "EFO:1002031", "mulitple keratinocyte carcinoma susceptibility measurement": "EFO:0007932", "regulation of cellular process": "GO:0050794", "Vulvar Squamous Cell Carcinoma": "EFO:1000624", "GM17294 {http": "CLO:0013138", "congenital left-sided heart lesions": "EFO:0005938", "Thyrotoxic periodic paralysis": "Orphanet:79102", "Spastic paraplegia type 2": "Orphanet:99015", "Zaire ebolavirus - Gabon (1994-1997)": "NCBITaxon:128947", "emphysema pattern measurement": "EFO:0005850", "response to homoharringtonine": "EFO:0006996", "SUM225CWN": "EFO:0001244", "leucine-induced hypoglycemia": "EFO:0006856", "alliin {http": "CHEBI:2596", "Cranial meningocele": "Orphanet:268820", "COLO 853": "EFO:0006380", "brain stem infarction": "EFO:1000847", "Autosomal recessive childhood-onset cortical cataract": "Orphanet:217046", "inguinal region": "UBERON:0008337", "MEG01": "EFO:0002232", "spotted antibody reporter": "EFO:0005074", "Encephaloclastic disorder": "Orphanet:269190", "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency": "Orphanet:314637", "pneumococcal infection": "EFO:0000772", "chronic rhinosinusitis without nasal polyps": "EFO:1002030", "Congenital bile acid synthesis defect": "EFO:0009039", "Hemoglobin C - beta-thalassemia": "Orphanet:231242", "lycopene measurement": "EFO:0007801", "GM17157 {http": "CLO:0013962", "mild neurocognitive disorder": "EFO:0007982", "Fragile X-associated tremor/ataxia syndrome": "Orphanet:93256", "B117P": "EFO:0002041", "femoral neck bone geometry": "EFO:0004511", "Idiopathic pulmonary arterial hypertension": "Orphanet:275766", "NCI-H2081": "EFO:0002276", "soluble transferrin receptor measurement": "EFO:0004460", "Selaginella moellendorffii": "NCBITaxon:88036", "Orofaciodigital syndrome type 2": "Orphanet:2751", "KCI-MOH1": "EFO:0006608", "B-type natriuretic peptide to N-terminal pro B-type natriuretic peptide ratio": "EFO:0008469", "Bacillus subtilis subsp. subtilis str. 168": "NCBITaxon:224308", "infraorbital lateral line neuromast": "UBERON:2000813", "Hyperkeratosis-hyperpigmentation syndrome": "Orphanet:1336", "follicle stimulating hormone measurement": "EFO:0004768", "Neurological conditions associated with aminoacylase 1 deficiency": "Orphanet:137754", "Nodulosis-arthropathy-osteolysis syndrome": "Orphanet:85196", "Simpson-Golabi-Behmel syndrome type 2": "Orphanet:79022", "Tracheal Squamous Cell Carcinoma": "EFO:1000600", "short-term memory": "EFO:0004335", "Trisomy 13": "Orphanet:3378", "Juvenile nephropathic cystinosis": "EFO:0009049", "rubella": "EFO:1002026", "merkel cell": "EFO:1001470", "pathogen test": "EFO:0000644", "Illumina HiSeq 3000": "EFO:0008564", "meristematic cell {http": "PO:0004010", "muscular disease": "EFO:0002970", "Syndromic gastroduodenal malformation": "Orphanet:108965", "calicheamicin gamma1(I)": "CHEBI:3319", "MLO-Y4": "EFO:0005394", "Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia": "Orphanet:1882", "Autosomal recessive isolated diffuse palmoplantar keratoderma": "Orphanet:98356", "Mycobacterium tuberculosis": "NCBITaxon:1773", "Hemophilia A": "Orphanet:98878", "Digestive duplication": "Orphanet:238", "Ehlers-Danlos syndrome, fibronectinemic type": "Orphanet:75501", "Temperature-sensitive oculocutaneous albinism type 1": "Orphanet:352737", "Avena sativa": "NCBITaxon:4498", "Hidrotic ectodermal dysplasia, Halal type": "Orphanet:1809", "Profiler": "EFO:0008870", "Scylla paramamosain": "NCBITaxon:85552", "premature birth": "EFO:0003917", "Cystinosis": "Orphanet:213", "Encephalopathy - hypertrophic cardiomyopathy - renal tubular disease": "Orphanet:319678", "Saccharum officinarum": "NCBITaxon:4547", "Genetic hyperpigmentation of the skin": "Orphanet:183466", "euploid {http": "PATO:0001393", "Rombo syndrome": "Orphanet:3110", "Helicobacter pylori P12": "NCBITaxon:570508", "B-2 B cell": "CL:0000822", "posterior cerebral artery infarction": "EFO:1001118", "46C {http": "EFO:0005484", "RMUG-S": "EFO:0006747", "Acromelic dysplasia": "Orphanet:93436", "Lactobacillus rhamnosus GG": "NCBITaxon:568703", "tacrolimus measurement": "EFO:0008458", "Epithelio-exfoliative colitis - deafness": "Orphanet:103912", "16-ketoestradiol": "CHEBI:34165", "Humero-radio-ulnar synostosis": "Orphanet:3266", "Presynaptic congenital myasthenic syndromes": "Orphanet:98914", "Pontocerebellar hypoplasia type 6": "Orphanet:166073", "Familial renal amyloidosis": "Orphanet:85450", "Autosomal recessive metabolic cerebellar ataxia": "Orphanet:98096", "Juvenile myoclonic epilepsy": "Orphanet:307", "dorsal histoblast nest abdominal": "UBERON:6001791", "interleukin 18 receptor accessory protein measurement": "EFO:0008179", "Trichoderma atroviride": "NCBITaxon:63577", "fasting blood insulin measurement": "EFO:0004466", "corneal edema": "EFO:1000879", "Severe neurodegenerative syndrome with lipodystrophy": "Orphanet:363400", "small intestine carcinoma": "EFO:0005588", "Radius absent - anogenital anomalies": "Orphanet:3016", "UCSD-242l": "EFO:0006769", "contrast sensitivity measurement": "EFO:0005419", "Gastric Mantle Cell Lymphoma": "EFO:1000272", "GR1307": "EFO:0004087", "Clostridium botulinum A str. ATCC 3502": "NCBITaxon:413999", "parietal lobe": "UBERON:0001872", "ankle injury": "EFO:1002021", "clinical modifier": "HP:0012823", "Histiocytoid cardiomyopathy": "Orphanet:137675", "discitis": "EFO:1000900", "GM17224 {http": "CLO:0014369", "Junctional epidermolysis bullosa, non-Herlitz type": "Orphanet:89840", "renal tubular transport disease": "EFO:1000647", "Microsporum gallinae": "NCBITaxon:69892", "post-concussion syndrome": "EFO:1001827", "human herpesvirus 8 seropositivity": "EFO:0007039", "fundus of stomach": "UBERON:0001160", "Spondyloepimetaphyseal dysplasia, Pakistani type": "Orphanet:93282", "Oncorhynchus tshawytscha": "NCBITaxon:74940", "RMG-I": "EFO:0006746", "RNAi library": "EFO:0007563", "process": "BFO:0000007", "Yersinia infectious disease": "EFO:1001245", "Escherichia coli BL21(DE3)": "NCBITaxon:469008", "IgG fucosylation measurement": "EFO:0008427", "response to norepinephrine-dopamine reuptake inhibitor": "EFO:0007870", "Pigmented paravenous retinochoroidal atrophy": "Orphanet:251295", "Conjunctival Squamous Cell Carcinoma": "EFO:1000206", "naive thymus-derived CD4-positive, alpha-beta T cell": "CL:0000895", "3-methylglutaconic aciduria type 4": "Orphanet:67048", "Qualitative or quantitative defects of merosin": "Orphanet:207094", "MS751": "EFO:0006456", "anterior lateral line system": "UBERON:2001468", "Popliteal pterygium syndrome": "Orphanet:294963", "X-linked intellectual disability, Shashi type": "Orphanet:85286", "TATL-seq": "EFO:0008963", "C-X-C motif chemokine 10 measurement": "EFO:0008056", "Von Willebrand disease type 2A": "Orphanet:166084", "Craniofaciofrontodigital syndrome": "Orphanet:363705", "SELEX-seq": "EFO:0008918", "picoliter": "UO:0000103", "polymyalgia rheumatica": "EFO:0008518", "superior temporal gyrus": "UBERON:0002769", "PA-1": "EFO:0006465", "N-acetyl-L-tryptophan {http": "CHEBI:74640", "Nitrosomonas europaea": "NCBITaxon:915", "1-methylinosine {http": "CHEBI:19065", "Pancreatic Glucagonoma": "EFO:1000441", "Joubert syndrome": "Orphanet:475", "Phosphaturic Mesenchymal Tumor": "EFO:1000473", "botulism": "EFO:0005542", "CB66": "EFO:0004073", "response to vitamin": "GO:0033273", "capillary leak syndrome": "EFO:1001284", "Infundibulopelvic stenosis - multicystic kidney": "Orphanet:1849", "ocimene": "EFO:0003191", "Cockayne syndrome": "Orphanet:191", "selenate": "CHEBI:15075", "3C": "EFO:0007689", "chloroplast envelope": "GO:0009941", "serum homoarginine measurement": "EFO:0005421", "Leigh syndrome with nephrotic syndrome": "Orphanet:255249", "3-phosphoserine phosphatase deficiency": "Orphanet:79350", "synovial membrane": "FMA:66762", "Episodic ataxia type 3": "Orphanet:79135", "CL-34": "EFO:0006369", "oleate {http": "CHEBI:30823", "Larsen-like syndrome, B3GAT3 type": "Orphanet:284139", "T1 B cell": "CL:0000958", "Cronobacter dublinensis": "NCBITaxon:413497", "Salmonella enterica subsp. enterica serovar Paratyphi B": "NCBITaxon:57045", "Ventricular Outflow Obstruction": "EFO:1001448", "vitamin B12 measurement": "EFO:0004620", "Meloidogyne graminicola {http": "NCBITaxon:189291", "Nephrosis - deafness - urinary tract - digital malformations": "Orphanet:2669", "radiation induced mutation": "EFO:0004500", "early onset hypertension": "EFO:0004772", "tyrosine kinase inhibitor": "CHEBI:38637", "Atypical Gaucher disease due to saposin C deficiency": "Orphanet:309252", "GM14467 {http": "CLO:0031276", "Rare male infertility due to adrenal disorder of genetic origin": "Orphanet:399994", "osteoradionecrosis": "EFO:1001821", "Homo sapiens": "NCBITaxon:9606", "Congenital absence/hypoplasia of thumb, unilateral": "Orphanet:295110", "21q22.11q22.12 microdeletion syndrome": "Orphanet:261323", "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency": "Orphanet:5", "Bone Anteversion": "EFO:1001274", "ethylene glycol": "CHEBI:30742", "caspofungin": "CHEBI:474180", "borderline leprosy": "EFO:0001055", "lymphocyte percentage of leukocytes": "EFO:0007993", "GM00038": "EFO:0004921", "Spinocerebellar ataxia with axonal neuropathy type 2": "Orphanet:64753", "Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies": "Orphanet:100049", "Hallux varus - preaxial polysyndactyly": "Orphanet:2110", "U-2932": "EFO:0006499", "bone marrow": "UBERON:0002371", "core binding factor acute myeloid leukemia": "EFO:1002001", "CC16 measurement": "EFO:0005080", "laryngeal tuberculosis": "EFO:0007337", "Kit-positive erythroid progenitor cell": "CL:0002000", "Oromandibular dystonia": "Orphanet:93958", "GM17747 {http": "CLO:0016565", "Salivary Gland Basal Cell Adenocarcinoma": "EFO:1000515", "S-formylglutathione hydrolase measurement": "EFO:0008275", "tiling array": "EFO:0002704", "response to simvastatin": "GO:1903491", "Distal trisomy 1p36": "Orphanet:96069", "Zinc": "CHEBI:27363", "CS57548": "EFO:0000011", "Atrial septal defect, sinus venosus type": "Orphanet:99105", "LoVo": "EFO:0006639", "HUES6": "EFO:0007086", "transplant outcome measurement": "EFO:0005198", "C-C motif chemokine 23 measurement": "EFO:0008049", "Hereditary cryohydrocytosis with normal stomatin": "Orphanet:398088", "complement factor H measurement": "EFO:0008097", "camphorsulfonic acid": "CHEBI:55379", "dihomo-linoleate (20": "CHEBI:88670", "periventricular grey zone": "UBERON:2000516", "WM-266-4": "EFO:0006774", "Mitochondrial DNA maintenance syndrome": "Orphanet:352456", "Mucopolysaccharidosis type 2": "Orphanet:580", "Phenotypic abnormality": "HP:0000118", "Tyrosinemia type 3": "Orphanet:69723", "Epsilon-(gamma-Glutamyl)-lysine {http": "CHEBI:88494", "Ring chromosome Y": "Orphanet:261529", "vascular endothelial growth factor receptor 3 measurement": "EFO:0008315", "Early-onset X-linked optic atrophy": "Orphanet:98890", "melanoma-derived growth regulatory protein measurement": "EFO:0008229", "vitamin D measurement": "EFO:0004631", "central nervous system AIDS arteritis": "EFO:0007198", "Hemangiopericytic Neoplasm": "EFO:1000289", "glutarate(1-) {http": "CHEBI:35907", "chronic gastritis": "EFO:0000337", "JeKo-1": "EFO:0005387", "felodipine": "CHEBI:585948", "hydronephrosis": "EFO:0005562", "Hemiparesis {http": "HP:0001269", "Atypical Carcinoid Tumor": "EFO:1000097", "LOC syndrome": "Orphanet:2407", "pathological gambling": "EFO:1001926", "Solanum lycopersicum": "NCBITaxon:4081", "muscle cancer": "EFO:0007384", "CS57896": "EFO:0000160", "Liver Diffuse Large B-Cell Lymphoma": "EFO:1000323", "Congenital disorder of glycosylation with intestinal involvement": "Orphanet:371188", "Monodelphis domestica": "NCBITaxon:13616", "brainstem": "UBERON:0002298", "Pfeiffer syndrome type 3": "Orphanet:93260", "Pineoblastoma": "EFO:1000475", "Baraitser-Winter syndrome": "Orphanet:2995", "Listeria monocytogenes serotype 4b str. F2365": "NCBITaxon:265669", "infectious myxomatosis": "EFO:0007327", "Illumina Genome Analyzer IIx": "EFO:0004202", "vulvar carcinoma": "EFO:0002921", "1-arachidonoyl-sn-glycerol {http": "CHEBI:34071", "Brevibacterium aurantiacum": "NCBITaxon:273384", "Rare eye disease due to a differentiation anomaly": "Orphanet:98558", "Schmidtea mediterranea": "NCBITaxon:79327", "ursodeoxycholate {http": "CHEBI:78604", "CD7-positive lymphoid progenitor cell": "CL:0001028", "Clostridium butyricum": "NCBITaxon:1492", "sunitinib": "CHEBI:38940", "gait measurement": "EFO:0007680", "symplectic": "UBERON:2000692", "anterior endoderm anlage in statu nascendi": "EFO:0000260", "epidermolysis bullosa acquisita": "EFO:1000691", "methylmercury": "CHEBI:49747", "INS-1": "EFO:0002529", "T-cell immunodeficiency with epidermodysplasia verruciformis": "Orphanet:324294", "3-carboxy-4-methyl-5-propyl-2-furanpropanoate {http": "CHEBI:82986", "glucose-dependent insulinotropic peptide measurement": "EFO:0008464", "ventral anterior lateral line ganglion": "UBERON:2001313", "lateral cord neuron": "FBbt:00005675", "Dominant hypophosphatemia with nephrolithiasis or osteoporosis": "Orphanet:244305", "Lactococcus lactis subsp. cremoris": "NCBITaxon:1359", "biliary dyskinesia": "EFO:0007169", "N-acetyl-L-histidine {http": "CHEBI:16437", "derived temperature unit": "UO:0000126", "Rare disease with dentinogenesis imperfecta": "Orphanet:167762", "CS57823": "EFO:0000131", "nervous system heavy metal poisoning": "EFO:1001815", "HiTS-Flip": "EFO:0008765", "monoatomic ion": "CHEBI:24867", "forearm": "UBERON:0002386", "copper(II) chloride": "CHEBI:49553", "Salmonella enterica subsp. indica": "NCBITaxon:59207", "thrombin-antithrombin complex measurement": "EFO:0007775", "Congenital disorder of glycosylation with dilated cardiomyopathy": "Orphanet:371176", "interleukin 4 measurement": "EFO:0008184", "DPM3-CDG": "Orphanet:263494", "paraphimosis": "EFO:1001086", "thyroid nodule": "EFO:1001436", "GM17744 {http": "CLO:0016568", "Autosomal dominant keratitis": "Orphanet:2334", "ethnic group": "EFO:0001799", "PMM2-CDG": "Orphanet:79318", "tetradecanedioate (2-) {http": "CHEBI:76281", "avian influenza": "EFO:0005222", "Human T-lymphotropic virus 1 infectious disease": "EFO:0007316", "cardiac muscle cell": "CL:0000746", "Hs 746T": "EFO:0006589", "Naegleria gruberi": "NCBITaxon:5762", "Tyrosinemia type 1": "Orphanet:882", "parathyroid": "CL:0000446", "Friedreich ataxia": "Orphanet:95", "silicon substrate": "EFO:0005065", "endocardium": "UBERON:0002165", "tibial neuropathy": "EFO:1001213", "immature Vgamma1.1-positive, Vdelta6.3-positive thymocyte": "CL:0002415", "Osteochondritis Dissecans": "HP:0010886", "Bacteroides infectious disease": "EFO:1000832", "Vitamin B12-responsive methylmalonic acidemia type cblA": "Orphanet:79310", "Meniere disease": "EFO:0006862", "Horizontal gaze palsy with progressive scoliosis": "Orphanet:2744", "interleukin": "EFO:0004100", "nicotinamide {http": "CHEBI:17154", "Disorder of serine or glycine metabolism": "Orphanet:79194", "gastric mucosal hypertrophy": "EFO:1000946", "Goniodysgenesis": "Orphanet:98633", "sodium chloride regimen": "EO:0007048", "CTS (Concatenated Tag Sequencing)": "EFO:0004162", "Glycogen storage disease due to hepatic glycogen synthase deficiency": "Orphanet:2089", "SET-2": "EFO:0006486", "ventral epidermis primordium": "UBERON:6005533", "GM17275 {http": "CLO:0013202", "Partial trisomy/tetrasomy of the short arm of chromosome 18": "Orphanet:262812", "squamous odontogenic tumor": "EFO:1001848", "activated CD8-positive, alpha-beta T cell": "CL:0000906", "Cerebro-facio-articular syndrome": "Orphanet:314679", "Mitochondrial myopathy": "Orphanet:206966", "apratoxin A": "CHEBI:35212", "mature CD11c-negative plasmacytoid dendritic cell": "CL:0000996", "Trichoodontoonychial dysplasia": "Orphanet:3355", "Disorder of glyoxylate metabolism": "Orphanet:308998", "Protein-losing enteropathy {http": "HP:0002243", "Congenital hydrocephalus": "Orphanet:2185", "isotretinoin": "CHEBI:6067", "Frontorhiny": "Orphanet:391474", "CAL120": "EFO:0005356", "survival probability": "EFO:0000715", "McCune-Albright syndrome": "Orphanet:562", "Partial deletion of chromosome 1": "Orphanet:261766", "Junctional epidermolysis bullosa inversa": "Orphanet:79405", "Dandy-Walker malformation - postaxial polydactyly": "Orphanet:1566", "CD4-negative, CD8-negative type I NK T cell": "CL:0000924", "response to haloperidol": "GO:1905119", "Gadus morhua": "NCBITaxon:8049", "essential thrombocythemia": "EFO:0000479", "organic substance biosynthetic process": "GO:1901576", "DSM-IV-based  non-social scale": "EFO:0004781", "Prog\u00c3\u00a9ria - short stature - pigmented nevi": "Orphanet:2959", "Brucella melitensis bv. 1 str. 16M": "NCBITaxon:224914", "Uniparental disomy of paternal origin": "Orphanet:98154", "Stramenopiles {http": "NCBITaxon:33634", "Ler-1": "EFO:0005155", "46,XX testicular disorder of sex development": "Orphanet:393", "CAROLI/EiJ": "EFO:0007839", "Familial melanoma": "Orphanet:618", "mental process": "EFO:0004323", "RKOE6": "EFO:0002318", "MT3": "EFO:0002241", "AG08048 {http": "CLO:0033570", "Sensorineural deafness with dilated cardiomyopathy": "Orphanet:217622", "Burkholderia lata": "NCBITaxon:482957", "GM17145 {http": "CLO:0013943", "ATTRV122I amyloidosis": "Orphanet:85451", "microgram per milliliter": "UO:0000274", "gonadal tissue neoplasm": "EFO:1000953", "mature dermal dendritic cell": "CL:0001010", "CD8-positive, alpha-beta cytotoxic T cell": "CL:0000794", "Col-7": "EFO:0006985", "ecthyma": "EFO:1000689", "byssinosis": "EFO:1000851", "embryonic structure": "UBERON:0002050", "meningococcal meningitis": "EFO:1001040", "Congenital shoulder dislocation": "Orphanet:295030", "GM17797 {http": "CLO:0016494", "myocardium": "UBERON:0002349", "delivery method": "EFO:0000395", "Autosomal recessive cutis laxa type 1": "Orphanet:90349", "carnitine {http": "CHEBI:17126", "croup": "EFO:0007227", "IP-seq": "EFO:0005032", "carbonic anhydrase 6 measurement": "EFO:0008068", "spongiotic dermatitis": "EFO:1000768", "Barth syndrome": "Orphanet:111", "prothoracic gland": "FBbt:00001724", "CS57737": "EFO:0000081", "Bazex syndrome": "Orphanet:166113", "Angelman syndrome due to maternal 15q11q13 deletion": "Orphanet:98794", "childhood eosinophilic esophagitis": "EFO:0004594", "embryonic tracheole": "FBbt:00005571", "Halobacterium salinarum": "NCBITaxon:2242", "disposition": "BFO:0000016", "cardiac edema": "EFO:1001771", "Brachydactyly type A6": "Orphanet:93382", "MACS syndrome": "Orphanet:217335", "vascular endothelial growth factor measurement": "EFO:0004762", "intercellular adhesion molecule 5 measurement": "EFO:0008164", "red blood cell distribution width": "EFO:0005192", "beta cell": "CL:0000168", "cell cycle": "GO:0007049", "tribenuron methyl": "CHEBI:9678", "Dicarboxylic aminoaciduria": "Orphanet:2195", "Arthroderma gypseum": "NCBITaxon:63402", "MIPSTR": "EFO:0008814", "Blepharophimosis-intellectual disability syndrome, Ohdo type": "Orphanet:2728", "ulnar neuropathy": "EFO:1001224", "Spina bifida aperta": "Orphanet:268369", "Carnitine-acylcarnitine translocase deficiency": "Orphanet:159", "exfoliation syndrome": "EFO:0004235", "Lethal infantile mitochondrial myopathy": "Orphanet:254857", "atopic march": "EFO:0007755", "Apparent mineralocorticoid excess": "Orphanet:320", "CADDS": "Orphanet:369942", "trunk mesenchyme": "UBERON:0005256", "Streptomyces scabiei": "NCBITaxon:1930", "nanogram per milliliter": "UO:0000275", "(S)-2-hydroxypalmitate {http": "CHEBI:75928", "ethmoid sinusitis": "EFO:0007264", "Posterior fusion of lumbosacral vertebrae - blepharoptosis": "Orphanet:2064", "pouchitis": "EFO:0003921", "Total autosomal trisomy": "Orphanet:98131", "mucosa of urinary bladder {http": "UBERON:0001259", "Isolated encephalocele": "Orphanet:199647", "arylsulfatase B measurement": "EFO:0008030", "orbital cellulitis": "EFO:1001076", "tauopathy": "EFO:0005815", "purine ribonucleoside monophosphate biosynthetic process": "GO:0009168", "Pachydermoperiostosis": "Orphanet:2796", "bronchial disease": "EFO:1002018", "Corynebacterium glutamicum ATCC 13032": "NCBITaxon:196627", "cyproheptadine hydrochloride": "CHEBI:59695", "plasma membrane": "GO:0005886", "Petromyzon marinus": "NCBITaxon:7757", "Niemann-Pick disease type E": "Orphanet:99022", "perinephritis": "EFO:1001099", "Listeria monocytogenes J0161": "NCBITaxon:393130", "cell culture": "BTO:0000214", "HT-ChIP": "EFO:0008768", "puberty onset measurement": "EFO:0005677", "Azoarcus sp.": "NCBITaxon:29544", "Granular corneal dystrophy type I": "Orphanet:98962", "attempted suicide": "EFO:0004321", "Sudan ebolavirus": "NCBITaxon:186540", "5,6-dihydrouracil {http": "CHEBI:15901", "Long eyelashes {http": "HP:0000527", "Myopathy due to calsequestrin and SERCA1 protein overload": "Orphanet:88635", "Glycerol kinase deficiency, infantile form": "Orphanet:284408", "Clark level IV": "EFO:0004960", "splenic infarction": "EFO:1001190", "Congenital alacrima": "Orphanet:98604", "facial neural processing": "EFO:0004914", "Borderline Fallopian Tube Serous Neoplasm": "EFO:1000134", "elafin measurement": "EFO:0008117", "mature NK T cell": "CL:0000814", "cannabis dependence measurement": "EFO:0008457", "anterior lateral plate mesoderm": "UBERON:0009881", "dorsal plus ventral thalamus": "UBERON:0001897", "Bazex-Dupr\u00c3\u00a9-Christol syndrome": "Orphanet:113", "Blackmount ecotype": "EFO:0007605", "antidepressant-induced hearing impairment": "EFO:0006324", "interleukin 1 Receptor accessory protein measurement": "EFO:0008167", "GCT": "EFO:0002182", "BNP measurement": "EFO:0006920", "Familial cutaneous collagenoma": "Orphanet:53296", "afferent loop syndrome": "EFO:1000799", "HuH-7": "EFO:0005384", "alpha-D-glucose": "CHEBI:17925", "JVM3": "EFO:0002214", "CD14-low, CD16-positive monocyte": "CL:0002396", "Digestive System Carcinoma": "EFO:1000218", "generation": "EFO:0000507", "Ballard syndrome": "Orphanet:93395", "carrier status": "EFO:0007658", "Dysarthria {http": "HP:0001260", "AG08046 {http": "CLO:0033577", "sebaceous gland neoplasm": "EFO:1001172", "LP.18 eighteen leaves visible stage": "PO:0007072", "Fallopian Tube Carcinosarcoma": "EFO:1000252", "diclofenac sodium": "CHEBI:4509", "Diffuse palmoplantar keratoderma-acrocyanosis syndrome": "Orphanet:86918", "Mosaic trisomy 7": "Orphanet:1747", "Volvox carteri": "NCBITaxon:3067", "Autosomal dominant limb-girdle muscular dystrophy type 1D": "Orphanet:34516", "gluconate {http": "CHEBI:24265", "Myelomeningocele": "Orphanet:93969", "Grubben-de Cock-Borghgraef syndrome": "Orphanet:2101", "Blepharoptosis - cleft palate - ectrodactyly - dental anomalies": "Orphanet:1258", "transcription profiling": "EFO:0001032", "Trichorhinophalangeal syndrome": "Orphanet:324764", "Motor stereotypies": "Orphanet:306765", "Tis": "EFO:0004947", "Rosa gallica": "NCBITaxon:74632", "pyelonephritis": "EFO:1001141", "Han Chinese": "EFO:0003161", "total blood protein measurement": "EFO:0004536", "3C syndrome": "Orphanet:7", "nervous system": "UBERON:0001016", "citrate(2-) {http": "CHEBI:35808", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation": "Orphanet:324611", "Paranasal Sinus Adenoid Cystic Carcinoma": "EFO:1000454", "polybrominated biphenyl measurement": "EFO:0007961", "2-hydroxypalmitate {http": "CHEBI:65097", "Pili torti - onychodysplasia": "Orphanet:2890", "Spondyloepiphyseal dysplasia tarda, Kohn type": "Orphanet:163665", "Anterior polar cataract": "Orphanet:98988", "Syndromic keratoconus": "Orphanet:98623", "Cough": "HP:0012735", "abnormality of the lung": "HP:0002088", "adenomatous colon polyp": "EFO:1000633", "maxillary neoplasm": "EFO:0007360", "Ring chromosome 19": "Orphanet:1443", "Drosophila mauritiana": "NCBITaxon:7226", "Spondylometaphyseal dysplasia, Schmidt type": "Orphanet:93316", "transferrin saturation measurement": "EFO:0006333", "Alopecia-intellectual disability syndrome": "Orphanet:2850", "phosphatidylethanolamine": "CHEBI:16038", "Caudal appendage - deafness": "Orphanet:1123", "rosacea": "EFO:1000760", "NB4": "EFO:0002798", "prostaglandin E2": "CHEBI:15551", "fresh specimen": "OBI:0000971", "adenosquamous lung carcinoma": "EFO:0000233", "Congenital laryngeal web": "Orphanet:2374", "plateletcrit": "EFO:0007985", "Primary membranoproliferative glomerulonephritis": "Orphanet:54370", "sexual dysfunction": "EFO:0004714", "methiothepin maleate": "CHEBI:64202", "Growth delay due to insulin-like growth factor type 1 deficiency": "Orphanet:73272", "Infantile myofibromatosis": "Orphanet:2591", "Ptosis - upper ocular movement limitation - absence of lacrimal punctum": "Orphanet:228396", "senile plaques": "HP:0100256", "Potassium-aggravated myotonia": "Orphanet:612", "HCC2302": "EFO:0006432", "Syndrome with microcephaly as major feature": "Orphanet:269528", "Dehalococcoides": "NCBITaxon:61434", "Zimmermann-Laband syndrome": "Orphanet:3473", "varicose ulcer": "EFO:1001923", "genotyping by array": "EFO:0002767", "Pituitary deficiency": "Orphanet:101957", "Spondyloepiphyseal dysplasia, Maroteaux type": "Orphanet:263482", "EDICT syndrome": "Orphanet:293936", "CS57719": "EFO:0000074", "huH-1": "EFO:0006445", "viral meningitis": "EFO:1001236", "Hyperinsulinism due to UCP2 deficiency": "Orphanet:276556", "RL952": "EFO:0002320", "Primary bone dysplasia with micromelia": "Orphanet:364536", "Hs 38.T": "EFO:0006586", "gastrula 80%-epiboly": "EFO:0002560", "software": "EFO:0002029", "Salmonella gastroenteritis": "EFO:0007475", "COLO205": "EFO:0003082", "ILSXISS#/Tej": "EFO:0002971", "X-linked intellectual disability-retinitis pigmentosa syndrome": "Orphanet:85332", "Neurogenic palpebral tumor": "Orphanet:98593", "GM12056": "EFO:0001134", "ovarian mucinous adenocarcinoma": "EFO:0006462", "Familial isolated arrhythmogenic ventricular dysplasia, biventricular form": "Orphanet:293899", "R46": "EFO:0001229", "Spinal Cord Primitive Neuroectodermal Tumor": "EFO:1000545", "software manufacturer": "EFO:0001740", "B6.Cg-Tg(SOD1-G93A)1Gur/J": "EFO:0001328", "Kin-0": "EFO:0006967", "angioedema": "EFO:0005532", "MRC5": "EFO:0002835", "heart aneurysm": "EFO:1000959", "stomatogastric nervous system primordium": "FBbt:00005536", "microgram per kilogram per day": "EFO:0002929", "immunosuppressive agent": "CHEBI:35705", "Retinoblastoma": "Orphanet:790", "tooth 3V": "UBERON:2001145", "antimetabolite role": "CHEBI:35221", "minimal erythema dose": "EFO:0007639", "adenoid cystic carcinoma": "EFO:0000231", "Acquired porencephaly": "Orphanet:314697", "Haliotis asinina": "NCBITaxon:109174", "Ictalurus punctatus": "NCBITaxon:7998", "MDAMB415": "EFO:0001212", "primitive neuroectodermal tumor": "EFO:0005235", "GM12866": "EFO:0005339", "ibuprofen {http": "CHEBI:5855", "GM08930 {http": "CLO:0011235", "acetonitrile": "CHEBI:38472", "Papio hamadryas": "NCBITaxon:9557", "nifedipine": "CHEBI:7565", "abdominal skin": "UBERON:0001416", "ALG3-CDG": "Orphanet:79321", "Paroxysmal non-kinesigenic dyskinesia": "Orphanet:98810", "Absent tibia - polydactyly - arachnoid cyst": "Orphanet:3328", "CPT-seq": "EFO:0008698", "CS57646": "EFO:0000051", "interleukin 6 receptor subunit alpha measurement": "EFO:0008187", "kwashiorkor": "EFO:1001009", "embryonic gastric caecum": "FBbt:00017027", "Primary congenital hypothyroidism without thyroid developmental anomaly": "Orphanet:95714", "Rhabdoid Meningioma": "EFO:1000511", "Heart defect-tongue hamartoma-polysyndactyly syndrome": "Orphanet:1338", "Theiler stage 10": "EFO:0004402", "HEC1B": "EFO:0002192", "response to cyclophosphamide": "GO:1902518", "oxirane": "CHEBI:27561", "clinical temporal measurement": "EFO:0004949", "facial emotion recognition measurement": "EFO:0008329", "oligodendrocyte": "CL:0000128", "response to antibiotic": "GO:0046677", "Ehlers-Danlos syndrome, hypermobility type": "Orphanet:285", "Clostridium beijerinckii": "NCBITaxon:1520", "reference design": "EFO:0001775", "Partial deletion of the short arm of chromosome 2": "Orphanet:261866", "Craniostenosis associated with a strabismus": "Orphanet:98684", "neonatal myasthenia gravis": "EFO:1001059", "Cerebral cortical dysplasia": "Orphanet:268950", "CS57733": "EFO:0000079", "Autosomal recessive pure spastic paraplegia": "Orphanet:100982", "interleukin 23 receptor measurement": "EFO:0008181", "X-linked syndromic intellectual disability": "Orphanet:98464", "Autosomal dominant cutis laxa": "Orphanet:90348", "Oculocutaneous albinism type 3": "Orphanet:79433", "Blast Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive": "EFO:1000131", "deciliter": "UO:0000209", "GM17219 {http": "CLO:0013924", "Partial trisomy of the long arm of chromosome 16": "Orphanet:262959", "Mus musculus domesticus": "NCBITaxon:10092", "Cryptococcus": "NCBITaxon:5415", "X-linked thrombocytopenia with normal platelets": "Orphanet:852", "5-fluorouracil": "CHEBI:46345", "pancreatic neuroendocrine tumor": "EFO:1000045", "Karenia brevis": "NCBITaxon:156230", "Treponema infectious disease": "EFO:1001217", "Recurrent infection due to specific granule deficiency": "Orphanet:169142", "Geobacillus sp. E263": "NCBITaxon:391290", "hyperestrogenism": "EFO:0009004", "FiT-Seq": "EFO:0008743", "Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus": "Orphanet:137608", "parasympatholytic": "CHEBI:50370", "CD4-positive, alpha-beta memory T cell": "CL:0000897", "induced T-regulatory cell": "CL:0000902", "organic cyclic compound biosynthetic process": "GO:1901362", "susceptibility to childhood ear infection measurement": "EFO:0007904", "Spastic paraplegia - glaucoma - intellectual disability": "Orphanet:2818", "metaplastic breast carcinoma": "EFO:1000040", "BFTC905": "EFO:0002115", "acinar cell": "CL:0000622", "Maternal uniparental disomy of chromosome 4": "Orphanet:96180", "Rare lacrimal system disease": "Orphanet:98602", "congenital contractures of the limbs and face, hypotonia, and developmental delay": "EFO:1001868", "Genetic neuromuscular disease": "Orphanet:183497", "array control design": "EFO:0005440", "body weight gain": "EFO:0004566", "Bovine viral diarrhea virus 1": "NCBITaxon:11099", "plant callus {http": "PO:0005052", "human oral metagenome": "NCBITaxon:447426", "miCLIP-m5A": "EFO:0008806", "liver CD103-positive dendritic cell": "CL:0002506", "thyroid disease": "EFO:1000627", "iron": "CHEBI:18248", "yeast media": "EFO:0007024", "Non-syndromic congenital cataract": "Orphanet:91492", "Rotor syndrome": "Orphanet:3111", "Sneeze": "HP:0025095", "inorganic pyrophosphatase measurement": "EFO:0008157", "Syndromic ichthyosis associated with ocular features": "Orphanet:98699", "Cyclic neutropenia": "Orphanet:2686", "lean body mass": "EFO:0004995", "Ovarian Endometrioid Adenocarcinoma": "EFO:1000416", "Rare genetic deafness": "Orphanet:96210", "Acute rhabdomyolysis {http": "HP:0008942", "alcohol amnestic disorder": "EFO:1001759", "scBS-seq": "EFO:0008905", "family history": "EFO:0000493", "Syndromic developmental defect of the eye": "Orphanet:108987", "Micrococcus luteus": "NCBITaxon:1270", "Familial adrenal hypoplasia with absent pituitary luteinizing hormone": "Orphanet:95700", "Ramon syndrome": "Orphanet:3019", "Ammon's horn": "UBERON:0001954", "rhinitis": "EFO:0008521", "C syndrome": "Orphanet:1308", "Laternula elliptica": "NCBITaxon:228457", "X-linked Opitz G/BBB syndrome": "Orphanet:306597", "mushroom workers' lung": "EFO:0007385", "X-linked osteoporosis with fractures": "Orphanet:391330", "Phodopus sungorus": "NCBITaxon:10044", "Partial duplication of the long arm of chromosome 2": "Orphanet:262842", "Metabolic disease involving other neurotransmitter deficiency": "Orphanet:79219", "clomipramine": "CHEBI:47780", "agoraphobia": "EFO:1001872", "Dent disease type 1": "Orphanet:93622", "parthenolide": "CHEBI:7939", "closed colony random bred strain": "EFO:0004001", "Mucopolysaccharidosis type 1": "Orphanet:579", "Staphylococcus aureus subsp. aureus MW2": "NCBITaxon:196620", "6q16 deletion syndrome": "Orphanet:171829", "event death": "EFO:0000480", "Nicotiana tabacum": "NCBITaxon:4097", "social communication impairment": "EFO:0005427", "Choroideremia": "Orphanet:180", "tooth 5V": "UBERON:2001142", "uterine prolapse": "EFO:1001864", "carbohydrate measurement": "EFO:0004998", "superior frontal gyrus": "UBERON:0002661", "Solanum pimpinellifolium": "NCBITaxon:4084", "specific language impairment": "EFO:1001510", "Vitis rotundifolia": "NCBITaxon:103349", "acute graft vs. host disease": "EFO:0004599", "Glucose intolerance": "HP:0000833", "ini-seq": "EFO:0008781", "Ehlers-Danlos syndrome, vascular type": "Orphanet:286", "ND04424 {http": "CLO:0033747", "alpha-2-HS-glycoprotein measurement": "EFO:0008020", "Bm2' B cell": "CL:0000964", "ALG8-CDG": "Orphanet:79325", "skin atrophy": "EFO:1000766", "Lissencephaly with cerebellar hypoplasia type B": "Orphanet:100012", "infant white matter volume measurement": "EFO:0008370", "Dysosteosclerosis": "Orphanet:1782", "Rare odontal or periodontal disorder": "Orphanet:164001", "butyrate": "CHEBI:17968", "gambling behaviour": "EFO:0004699", "akinetic mutism": "EFO:0007138", "Acute infantile liver failure-multisystemic involvement syndrome": "Orphanet:370088", "1A2": "EFO:0002094", "cell part": "GO:0044464", "Prochlorococcus marinus str. MIT 9515": "NCBITaxon:167542", "GM14153 {http": "CLO:0034375", "Nasal Cavity Polyp": "EFO:1000391", "Gamma-glutamyl transpeptidase deficiency": "Orphanet:33573", "MV4II": "EFO:0002242", "Single transverse palmar crease {http": "HP:0000954", "Narrow chest {http": "HP:0000774", "GM12234": "EFO:0001142", "Macacine herpesvirus 3": "NCBITaxon:47929", "terpene": "CHEBI:35186", "Cerebellar ataxia, Cayman type": "Orphanet:94122", "Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell": "CL:0002454", "Connective tissue disease with eye involvement": "Orphanet:98702", "Deoxyribonuclease digestion": "EFO:0004186", "Focal facial dermal dysplasia type I": "Orphanet:79133", "vascular brain injury": "EFO:0006791", "Primary bone dysplasia": "Orphanet:364526", "N-acetyl-L-valine {http": "CHEBI:21565", "count unit": "UO:0000189", "Flynn-Aird syndrome": "Orphanet:2047", "CD56-bright cytokine secreting natural killer cell": "CL:0000938", "Ralstonia solanacearum GMI1000": "NCBITaxon:267608", "Genetic syndrome with a central nervous system malformation as major feature": "Orphanet:269564", "Aicardi syndrome": "Orphanet:50", "Typical nemaline myopathy": "Orphanet:171436", "adenocarcinoma": "EFO:0000228", "Cranio-cervical dystonia with laryngeal and upper-limb involvement": "EFO:0009040", "hindlimb": "UBERON:0002103", "urothelium cell line": "EFO:0005913", "Genetic infertility": "Orphanet:275742", "NCI-H345": "EFO:0006692", "extracellular region part": "GO:0044421", "uremia": "EFO:1001226", "Double outlet right ventricle with doubly committed ventricular septal defect": "Orphanet:99047", "SiMSen-Seq": "EFO:0008923", "icosapentaenoic acid {http": "CHEBI:36006", "calcium(2+)": "CHEBI:29108", "pulmonary function measurement": "EFO:0003892", "Pontocerebellar hypoplasia type 3": "Orphanet:97249", "peripheral vein": "EFO:0004923", "Wistar": "EFO:0001342", "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1": "Orphanet:177901", "Primary Effusion Lymphoma": "EFO:1000491", "GM12813": "EFO:0001156", "Isolated focal cortical dysplasia type Ic": "Orphanet:268987", "Morbillivirus infectious disease": "EFO:0007377", "Global brain atrophy {http": "HP:0002283", "axial hypoblast": "UBERON:2001378", "central nervous system cyst": "EFO:0003760", "KURAMOCHI": "EFO:0006625", "Myzus persicae": "NCBITaxon:13164", "glucose effectiveness measurement": "EFO:0006833", "Melorheostosis with osteopoikilosis": "Orphanet:1879", "Testicular Granulosa Cell Tumor": "EFO:1000567", "Dyssegmental dysplasia, Silverman-Handmaker type": "Orphanet:1865", "C. elegans embryo stage": "EFO:0005858", "neurodermatitis": "EFO:1000740", "T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency": "Orphanet:169154", "Linum usitatissimum": "NCBITaxon:4006", "beta-amyloid 1-42 measurement": "EFO:0004670", "Disseminated Peritoneal Leiomyomatosis": "EFO:1000220", "Alternating hemiplegia": "Orphanet:209978", "GM10845 {http": "CLO:0023783", "5-HIAA": "CHEBI:27823", "Progeroid and marfanoid aspect-lipodystrophy syndrome": "Orphanet:300382", "Avascular necrosis of genetic origin": "Orphanet:399388", "myelodysplastic syndrome": "EFO:0000198", "Neural tube closure defect": "Orphanet:268357", "extrinsic allergic alveolitis": "EFO:1001321", "Meleagris gallopavo": "NCBITaxon:9103", "Genetic digestive tract malformation": "Orphanet:183545", "neutrophilic myelocyte": "CL:0000580", "Congenital hereditary endothelial dystrophy type II": "Orphanet:293603", "Inherited isolated adrenal insufficiency due to CYP11A1 deficiency": "Orphanet:289548", "Geospiza conirostris": "NCBITaxon:48882", "glycolithocholate {http": "CHEBI:60008", "Rare genetic diabetes mellitus": "Orphanet:183625", "GM17839 {http": "CLO:0016523", "biotin": "CHEBI:15956", "Abdominal symptom": "HP:0011458", "Sulfolobus acidocaldarius DSM 639": "NCBITaxon:330779", "Congenital deformities of limbs": "Orphanet:294944", "Athabaskan brainstem dysgenesis syndrome": "Orphanet:69739", "Coloboma of choroid and retina": "Orphanet:98942", "D341Med": "EFO:0002157", "appendiceal neoplasm": "EFO:0003880", "response to losartan": "EFO:0006518", "CD8-alpha alpha positive, gamma-delta intraepithelial T cell": "CL:0000802", "Funaria hygrometrica": "NCBITaxon:29583", "Pachygyria - intellectual disability - epilepsy": "Orphanet:2798", "Griscelli disease": "Orphanet:381", "mature Vgamma2-negative thymocyte": "CL:0002409", "bladder tumor": "EFO:0000294", "Hydrocephalus with stenosis of the aqueduct of Sylvius": "Orphanet:2182", "Skin Cavernous Hemangioma": "EFO:1000530", "response to paliperidone": "EFO:0007925", "X-linked intellectual disability, Vitale type": "Orphanet:85289", "Arachnoid cyst": "Orphanet:2356", "Secondary dysgenetic glaucoma": "Orphanet:98631", "intermittent Staphylococcus aureus carrier status": "EFO:0007758", "IVIC syndrome": "Orphanet:2307", "lymph node tuberculosis": "EFO:0007350", "Autosomal dominant limb-girdle muscular dystrophy": "Orphanet:102014", "Hereditary North American Indian childhood cirrhosis": "Orphanet:168583", "Classic Mayer-Rokitansky-K\u00c3\u00bcster-Hauser syndrome": "Orphanet:247775", "neuroendocrine cell": "CL:0000165", "C-C motif chemokine 17 measurement": "EFO:0008045", "Magnaporthe oryzae 70-15": "NCBITaxon:242507", "microRNA profiling by RT-PCR": "EFO:0007687", "Acanthamoeba polyphaga mimivirus": "NCBITaxon:212035", "DOHH2": "EFO:0002167", "ML-DmD20-c2": "EFO:0005827", "Middle Ear Squamous Cell Carcinoma": "EFO:1000378", "PEO6": "EFO:0005449", "prediabetes syndrome": "EFO:1001121", "cot filtration for single or low copy genomic DNA": "EFO:0004171", "micronutrient": "CHEBI:27027", "HMEpC cell": "BTO:0002178", "MHHPREB1": "EFO:0002235", "Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature": "Orphanet:98353", "inhalation anaesthetic": "CHEBI:38870", "GM15227 {http": "CLO:0027473", "FGFR2-related bent bone dysplasia": "Orphanet:313855", "hydroxyzine": "CHEBI:5818", "O-adipoylcarnitine {http": "CHEBI:68568", "Craniotelencephalic dysplasia": "Orphanet:1528", "listeriolysin": "EFO:0003294", "Drosophila embryo stage": "EFO:0005859", "synthetic construct": "NCBITaxon:32630", "GM15386 {http": "CLO:0026786", "MT3847": "EFO:0004058", "1,1'-azobis(N,N-dimethylformamide)": "CHEBI:48958", "Malignant Breast Phyllodes Tumor": "EFO:0008545", "Angioleiomyoma": "EFO:1000084", "Hereditary thrombophilia due to congenital antithrombin deficiency": "Orphanet:82", "Sensorineural hearing loss - early graying - essential tremor": "Orphanet:66633", "perineum": "UBERON:0002356", "Pongo pygmaeus pygmaeus": "NCBITaxon:9602", "basal cell neoplasm": "EFO:1001763", "Primary Fanconi syndrome": "Orphanet:3337", "Progressive non-infectious anterior vertebral fusion": "Orphanet:2062", "GM13976": "EFO:0005345", "epidural neoplasm": "EFO:1000923", "calciol": "CHEBI:28940", "Acrokeratoelastoidosis of Costa": "Orphanet:38", "ventral mesenchyme": "UBERON:2000164", "carbon monoxide exhalation measurement": "EFO:0006520", "abnormality of vitamin metabolism": "HP:0100508", "non-word reading": "EFO:0005299", "ATC Code L Antineoplastic and immunomodulating agents": "EFO:0005641", "Paxillus involutus": "NCBITaxon:71150", "Partial monosomy of the short arm of chromosome X": "Orphanet:263731", "Charcot-Marie-Tooth disease type 1": "Orphanet:65753", "Argininemia": "Orphanet:90", "HERNS syndrome": "Orphanet:63261", "Autosomal dominant Emery-Dreifuss muscular dystrophy": "Orphanet:98853", "SJCRH30": "EFO:0005722", "Staphylococcus aureus": "NCBITaxon:1280", "fungal component": "EFO:0000788", "Illumina MiSeq": "EFO:0004205", "cytoplasmic membrane-bounded vesicle": "GO:0016023", "recalcitrant atopic dermatitis": "EFO:1000651", "Inclusion body myopathy with Paget disease of bone and frontotemporal dementia": "Orphanet:52430", "erythrocytic schizont": "EFO:0002591", "AG14446 {http": "CLO:0022320", "Bay-0": "EFO:0005175", "Metaphyseal chondrodysplasia, Schmid type": "Orphanet:174", "IgA pemphigus": "EFO:0008604", "Genetic cerebral malformation": "Orphanet:269553", "substantia nigra and ventral tegmental area": "EFO:0002528", "Pseudohypoaldosteronism type 2C": "Orphanet:88940", "Neisseria lactamica": "NCBITaxon:486", "embryonic day 18.5": "EFO:0002570", "ILSXISS86/TejJ": "EFO:0002995", "Zymoseptoria tritici IPO323 {http": "NCBITaxon:336722", "TAB-Seq": "EFO:0008958", "myxoid liposarcoma": "EFO:0000613", "ribonucleoside triphosphate biosynthetic process": "GO:0009201", "Punctate palmoplantar keratoderma": "Orphanet:307967", "postprandial hypotension": "EFO:0005253", "NCI-H2369": "EFO:0006678", "GM14568 {http": "CLO:0031580", "cardiovascular drug": "CHEBI:35554", "Miscellaneous movement disorder due to genetic neurodegenerative disease": "Orphanet:307058", "effector memory CD4-positive, alpha-beta T cell": "CL:0000905", "Alexandrium tamarense": "NCBITaxon:2926", "precursor": "EFO:0001651", "ligament rupture": "EFO:1002012", "Panc 03.27": "EFO:0006467", "xanthine {http": "CHEBI:15318", "malignant peritoneal mesothelioma": "EFO:0005567", "Primary syringomyelia": "Orphanet:99856", "Helicobacter pylori infectious disease": "EFO:1000961", "erythrocyte indices": "EFO:0004306", "Non-syndromic limb reduction defect": "Orphanet:93457", "5-oxoproline {http": "CHEBI:16010", "sodium chloride": "CHEBI:26710", "Tobacco mosaic virus": "NCBITaxon:12242", "Channelopathy-associated congenital insensitivity to pain": "Orphanet:88642", "lutein measurement": "EFO:0007895", "BG02ES": "EFO:0002778", "L1 larva": "EFO:0005508", "Osteogenesis imperfecta type 5": "Orphanet:216828", "peritoneal neoplasm": "EFO:1001100", "Ellis Van Creveld syndrome": "Orphanet:289", "pigmented spindle cell nevus": "EFO:1001105", "Calu1": "EFO:0002151", "LN-18": "EFO:0006636", "Familial lambdoid synostosis": "Orphanet:3267", "Antenatal multiminicore disease with arthrogryposis multiplex congenita": "Orphanet:178148", "Marfan and Marfan-related disorder": "Orphanet:284993", "follicular B cell": "CL:0000843", "amelanotic skin melanoma": "EFO:0002894", "Syndrome associated with Pierre Robin syndrome": "Orphanet:138063", "Gerbode defect": "Orphanet:99095", "Pterygium colli - intellectual disability - digital anomalies": "Orphanet:2988", "F4/80-positive adipose macrophage": "CL:0002479", "dimethyl sulfoxide": "CHEBI:28262", "anal pad specific anlage": "EFO:0000254", "minimally differentiated acute myeloblastic leukemia": "EFO:0003026", "pharyngeal pouch": "UBERON:0004117", "Corticobasal degeneration": "Orphanet:278", "4-hydroxybutyric aciduria": "Orphanet:22", "limited nitrate regimen {http": "EO:0001054", "Rare genetic urogenital disease": "Orphanet:156619", "interleukin-2 (Mus musculus)": "EFO:0003292", "head": "UBERON:0000033", "Paternal uniparental disomy of chromosome X": "Orphanet:261524", "complement C3d subcomponent measurement": "EFO:0008542", "Gorlin syndrome": "Orphanet:377", "Familial partial lipodystrophy associated with PPARG mutations": "Orphanet:79083", "cold urticaria": "EFO:1001881", "esophagogastric junction {http": "UBERON:0007650", "Proximal symphalangism": "Orphanet:3250", "imidacloprid": "CHEBI:5870", "Human immunodeficiency virus": "NCBITaxon:12721", "visual anlage in statu nascendi": "UBERON:6005425", "metabolic process": "GO:0008152", "Escherichia coli B": "NCBITaxon:37762", "Genetic urogenital tumor": "Orphanet:271844", "granulocyte percentage of myeloid white cells": "EFO:0007997", "sample treatment protocol": "EFO:0003809", "C57BL/6": "EFO:0004472", "Acute intermittent porphyria": "Orphanet:79276", "rib {http": "UBERON:0002228", "Bartonella quintana": "NCBITaxon:803", "Apis cerana": "NCBITaxon:7461", "Hyperdibasic aminoaciduria type 1": "Orphanet:1032", "mesenchyme pectoral fin": "UBERON:0003934", "3-methylbenzyl alcohol": "CHEBI:27995", "mediator of RNA polymerase II transcription subunit 1 measurement": "EFO:0008228", "serum galactose-deficient IgA1 measurement": "EFO:0007947", "Autosomal dominant medullary cystic kidney disease without hyperuricemia": "Orphanet:88949", "hepatocyte growth factor activator measurement": "EFO:0008152", "arabitol {http": "CHEBI:22605", "NanoCAGE": "EFO:0008824", "Tossa de Mar ecotype": "EFO:0006961", "UACC893": "EFO:0002385", "Oculocerebrorenal syndrome": "Orphanet:534", "caudal tuberculum": "UBERON:2000633", "dorsal longitudinal anastomotic vessel": "UBERON:2005025", "pelvic lipomatosis": "EFO:1000748", "RT-112": "EFO:0006479", "Autosomal recessive limb-girdle muscular dystrophy type 2M": "Orphanet:206554", "Rare thrombotic disorder due to a constitutional coagulation factors defect": "Orphanet:248361", "Partial deletion of chromosome 4": "Orphanet:261781", "Delayed puberty {http": "HP:0000823", "Familial isolated restrictive cardiomyopathy": "Orphanet:75249", "Inverse Klippel-Tr\u00c3\u00a9naunay syndrome": "Orphanet:329324", "role": "BFO:0000023", "salt treatment {http": "EO:0007185", "nicotine dependence": "EFO:0003768", "Rhodospirillum rubrum": "NCBITaxon:1085", "Macrocephaly - immune deficiency - anemia": "Orphanet:94061", "MKN7": "EFO:0002895", "454 GS FLX sequencer": "EFO:0004432", "Hereditary inclusion body myopathy type 4": "Orphanet:324381", "metabolic syndrome": "EFO:0000195", "Tetrasomy 21": "Orphanet:96055", "Progressive demyelinating neuropathy with bilateral striatal necrosis": "Orphanet:217396", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E": "Orphanet:93114", "4-methyl-2-oxopentanoate {http": "CHEBI:17865", "Von Willebrand disease type 3": "Orphanet:166096", "intussusception": "HP:0002576", "sensory system": "UBERON:0001032", "Acrofacial dysostosis, Kennedy-Teebi type": "Orphanet:64542", "mycelium": "BTO:0001436", "HOS": "EFO:0002196", "Nicotiana attenuata": "NCBITaxon:49451", "Gastrointestinal stromal tumor": "Orphanet:44890", "organonitrogen compound metabolic process": "GO:1901564", "ventral midline neuroblast": "FBbt:00005565", "Partial duplication of the long arm of chromosome 11": "Orphanet:262923", "epithelium of conjunctiva {http": "UBERON:0006763", "femtometer": "EFO:0001721", "Parkinsonian-pyramidal syndrome": "Orphanet:171695", "immature NK T cell stage IV": "CL:0002042", "Breast Mucosa-Associated Lymphoid Tissue Lymphoma": "EFO:1000146", "thymol sulfate {http": "CHEBI:82911", "drug-Induced dyskinesia": "EFO:1000904", "Multiminicore myopathy": "Orphanet:598", "angiotensin-converting enzyme inhibitor": "CHEBI:35457", "postoptic commissure": "UBERON:0003936", "serum dimethylarginine measurement": "EFO:0005418", "Rare genetic eye disease": "Orphanet:101435", "milli-International Unit per milliliter": "EFO:0004379", "Bean pod mottle virus": "NCBITaxon:12260", "creatinine": "CHEBI:16737", "Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome": "Orphanet:397618", "cecum adenocarcinoma": "EFO:1000020", "Mucopolysaccharidosis": "Orphanet:79213", "cis-aconitate(3-)": "CHEBI:16383", "blood nickel measurement": "EFO:0007583", "SRD5A3-CDG": "Orphanet:324737", "Congenital pseudoarthrosis of the tibia": "Orphanet:295018", "renal pelvis carcinoma": "EFO:0005582", "Autosomal dominant Charcot-Marie-Tooth disease type 2D": "Orphanet:99938", "Genetic neurodegenerative disease": "Orphanet:183500", "hyperemia": "EFO:0003822", "superior colliculus": "UBERON:0001945", "promyelocyte": "CL:0000836", "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency": "Orphanet:401948", "Partial trisomy of chromosome 20": "Orphanet:262692", "Scapuloperoneal amyotrophy": "Orphanet:85146", "panic disorder with agoraphobia": "EFO:1001906", "Francisella tularensis": "NCBITaxon:263", "Pro-Hyp {http": "CHEBI:74767", "LCLC-97TM1": "EFO:0006635", "Autosomal recessive spastic paraplegia type 46": "Orphanet:320391", "Combined oxidative phosphorylation defect type 21": "EFO:0009032", "Genetic hypopigmentation of the skin": "Orphanet:183469", "Syndromic hypothyroidism": "Orphanet:177107", "Proximal 16p11.2 microdeletion syndrome": "Orphanet:261197", "trochlear nerve disease": "EFO:1001220", "hydrogen peroxide": "CHEBI:16240", "Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome": "Orphanet:397973", "NCI-H187": "EFO:0002269", "midregional pro atrial natriuretic peptide measurement": "EFO:0008468", "amisulpride": "CHEBI:64045", "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency": "Orphanet:319558", "GM12891": "EFO:0002785", "Neurocutaneous syndrome with epilepsy": "Orphanet:166466", "acute insulin response measurement": "EFO:0006831", "tracheobronchial amyloidosis": "EFO:1001922", "lichen disease": "EFO:1000724", "AXIN2-related attenuated familial adenomatous polyposis": "Orphanet:401911", "mature CD8_alpha-negative CD11b-positive dendritic cell": "CL:0001003", "Autosomal recessive limb-girdle muscular dystrophy type 2I": "Orphanet:34515", "Cervical Adenoid Basal Carcinoma": "EFO:1000160", "Single ventricular septal defect": "Orphanet:99097", "enzyme inhibitor": "CHEBI:23924", "musculo-skeletal system cell": "EFO:0002956", "central nervous system macrophage": "CL:0000878", "retinal drusen": "EFO:1001155", "Isolated ectopia lentis": "Orphanet:1885", "Recombinant 8 syndrome": "Orphanet:96167", "cognitive inhibition measurement": "EFO:0007969", "aggressive behaviour measurement": "EFO:0007826", "genitourinary system": "UBERON:0004122", "gastroschisis": "EFO:1000949", "SCMDA": "EFO:0008910", "Proximal spinal muscular atrophy type 1": "Orphanet:83330", "sensory perception": "GO:0007600", "single-organism metabolic process": "GO:0044710", "gram per kilogram per day": "EFO:0004371", "Congenital isolated ACTH deficiency": "Orphanet:199296", "SUDHL16": "EFO:0002355", "poorly differentiated follicular thyroid carcinoma": "EFO:1002016", "phenylacetylglutamine {http": "CHEBI:25982", "Streptomyces rimosus": "NCBITaxon:1927", "Metachromatic leukodystrophy, juvenile form": "Orphanet:309263", "CD34-positive, CD38-positive common myeloid progenitor": "CL:0001026", "streptococcal pharyngitis": "EFO:1002024", "Disorder of lysosomal amino acid transport": "Orphanet:79207", "Bisulfite-seq": "EFO:0003753", "Mesomelic dwarfism, Nievergelt type": "Orphanet:2633", "Zenker diverticulum": "EFO:1001867", "serum carcinoembryonic antigen measurement": "EFO:0005760", "P-nitrotoluene": "CHEBI:33097", "Drosophila developmental tissue": "EFO:0003333", "tumor necrosis factor receptor superfamily member 19L measurement": "EFO:0008309", "GM07034": "EFO:0001112", "Generalized epilepsy - paroxysmal dyskinesia": "Orphanet:79137", "Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature": "Orphanet:371064", "SCC-3": "EFO:0006484", "imaginal disc": "FBbt:00001761", "Stickler syndrome type 3": "Orphanet:166100", "Hereditary persistence of fetal hemoglobin - sickle cell disease": "Orphanet:251380", "sex cord-stromal tumor": "EFO:1000052", "Escherichia coli meningitis": "EFO:1000929", "Familial abdominal aortic aneurysm": "Orphanet:86", "Vulvar Lichen Sclerosus": "EFO:1000623", "Childhood apraxia of speech": "Orphanet:209908", "Chlamydia trachomatis": "NCBITaxon:813", "Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome": "Orphanet:300333", "cutaneous squamous cell carcinoma": "EFO:1001927", "CD8_alpha-positive CD11b-negative dendritic cell": "CL:0001000", "German syndrome": "Orphanet:2077", "glucose tolerance test": "EFO:0004307", "late-onset myasthenia gravis": "EFO:1001490", "Atypical dentin dysplasia due to SMOC2 deficiency": "Orphanet:314721", "Rare genetic hematologic disease": "Orphanet:158300", "Candidemia": "EFO:1001282", "helper T cell": "CL:0000912", "Developmental anomaly of metabolic origin": "Orphanet:139009", "Methanobacterium": "NCBITaxon:2160", "Congenital ectropion uveae": "Orphanet:91491", "Mitochondrial substrate carrier disorder": "Orphanet:254830", "Undifferentiated Gallbladder Carcinoma": "EFO:1000604", "BMI-adjusted adiponectin measurement": "EFO:0007737", "biological variation design": "EFO:0004667", "GM17203 {http": "CLO:0013836", "capillary endothelial cell": "CL:0002144", "Cryptosporidiosis - chronic cholangitis - liver disease": "Orphanet:357329", "ductal carcinoma in situ": "EFO:0000432", "Deafness - enamel hypoplasia - nail defects": "Orphanet:3220", "Mucopolysaccharidosis type 6, rapidly progressing": "Orphanet:276212", "Hantaan virus": "NCBITaxon:11599", "Hyperphosphatasia-intellectual disability syndrome": "Orphanet:247262", "purine ribonucleoside monophosphate metabolic process": "GO:0009167", "X small rings": "Orphanet:96201", "Ear-patella-short stature syndrome": "Orphanet:2554", "raloxifene": "CHEBI:8772", "dysplastic oral keratinocyte": "EFO:0006566", "midgut": "UBERON:0001045", "p-cresol sulfate {http": "CHEBI:82914", "non-steroidal anti-inflammatory drug": "CHEBI:35475", "3'T-fill": "EFO:0008640", "L-363": "EFO:0006450", "nimesulide": "CHEBI:44445", "Hypoglossia/aglossia": "Orphanet:156212", "collection latitude": "EFO:0005020", "Ruegeria pomeroyi": "NCBITaxon:89184", "mitral valve stenosis": "EFO:0007372", "posterior lateral line": "UBERON:0006334", "infectious ectromelia": "EFO:0007325", "ciliary marginal zone": "UBERON:0003065", "pallidum volume": "EFO:0006933", "Cystinuria": "Orphanet:214", "hepatic stellate cell": "CL:0000632", "sulfhemoglobinemia": "EFO:1001200", "cleithrum": "UBERON:0004741", "Hereditary sensory and autonomic neuropathy type 5": "Orphanet:64752", "GM07029 {http": "CLO:0036870", "arrayer": "OBI:0400105", "pyruvate carboxylase deficiency disease": "EFO:1001142", "Brassica rapa subsp. pekinensis": "NCBITaxon:51351", "trichuriasis": "EFO:0007524", "processed array data file": "EFO:0004096", "ectonucleoside triphosphate diphosphohydrolase 5 measurement": "EFO:0008115", "celiac disease": "EFO:0001060", "Isolated Pierre Robin syndrome": "Orphanet:718", "foregut anlage": "FBbt:00005431", "Papillary Cystic Neoplasm": "EFO:1000448", "nimodipine": "CHEBI:7575", "Endometrial Serous Adenocarcinoma": "EFO:1000238", "Distal monosomy 12q": "Orphanet:96149", "quercetin": "CHEBI:16243", "Achromatopsia": "Orphanet:49382", "treatment outcome measurement": "EFO:0008383", "Peritoneal Multicystic Mesothelioma": "EFO:1000468", "Moyamoya disease with early-onset achalasia": "Orphanet:401945", "liver": "UBERON:0002107", "branchiostegal ray 3": "UBERON:2001280", "anatomy basic component": "EFO:0000786", "hatching stage": "EFO:0001298", "necatoriasis": "EFO:0007390", "fibroblast growth factor basic measurement": "EFO:0008130", "immature natural killer cell": "CL:0000823", "vitamin A": "CHEBI:12777", "mesonephros": "UBERON:0000080", "Conjunctival Melanoma": "EFO:1000204", "tissue plasminogen activator measurement": "EFO:0004791", "TL-seq": "EFO:0008972", "Becker nevus syndrome": "Orphanet:64755", "GBA carrier status": "EFO:0007698", "fenoldopam": "CHEBI:5002", "Paroxysmal extreme pain disorder": "Orphanet:46348", "alveolar soft part sarcoma": "EFO:0007143", "cellular protein metabolic process": "GO:0044267", "Cataract-microcornea syndrome": "Orphanet:1377", "GM12801": "EFO:0005353", "Cartilage-hair hypoplasia": "Orphanet:175", "hyperpituitarism": "EFO:1000973", "temperature unit": "UO:0000005", "Hypochondroplasia": "Orphanet:429", "Congenital absence of both forearm and hand, unilateral": "Orphanet:295093", "interleukin 27 receptor subunit alpha measurement": "EFO:0008183", "Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency": "Orphanet:70592", "coccidioidomycosis": "EFO:0007211", "mature eosinophil": "CL:0000041", "response to beta blocker": "EFO:0007766", "genomic measurement": "EFO:0004554", "Odonto-tricho-ungual-digito-palmar syndrome": "Orphanet:69082", "light": "EFO:0000568", "shoot component": "EFO:0001948", "infected cell": "BTO:0000152", "B220-positive CD38-negative unswitched memory B cell": "CL:0002112", "resting metabolic rate measurement": "EFO:0008004", "Postaxial polydactyly type B, unilateral": "Orphanet:295167", "1-O-hexadecyl-2-arachidonoyl-sn-glycero-3-phosphocholine {http": "CHEBI:55430", "abdominal aortic artery calcification": "EFO:0004859", "PacBio RS II": "EFO:0008631", "Autosomal recessive nail dysplasia": "Orphanet:280654", "GM17167 {http": "CLO:0013989", "NCI-H2795": "EFO:0006685", "lymphatic part of lymphoid system": "UBERON:0006558", "NCI-H2106": "EFO:0006672", "X-linked reticulate pigmentary disorder with systemic manifestations": "Orphanet:85453", "VACTERL with hydrocephalus": "Orphanet:3412", "Combined oxidative phosphorylation defect type 14": "Orphanet:319519", "Mesomelic dwarfism, Reinhardt-Pfeiffer type": "Orphanet:2634", "lateral cord glia": "FBbt:00005673", "Meconium ileus {http": "HP:0004401", "milligram": "UO:0000022", "MFM-223": "EFO:0006649", "CD11b-low, CD103-negative, langerin-negative lymph node dendritic cell": "CL:0002511", "Apolipoprotein A-I deficiency": "Orphanet:425", "response to non-steroidal anti-inflammatory": "EFO:0005533", "organonitrogen compound biosynthetic process": "GO:1901566", "meningeal macrophage": "CL:0000879", "carbohydrate metabolic process": "GO:0005975", "exercise test": "EFO:0004328", "pancreatic mesenchyme": "EFO:0002557", "ACTH-Producing Pituitary Gland Carcinoma": "EFO:1000067", "susceptibility to pneumonia measurement": "EFO:0008410", "Methanobrevibacter ruminantium": "NCBITaxon:83816", "afamin measurement": "EFO:0008015", "Ovarian Serous Adenofibroma": "EFO:1000428", "Rare non-syndromic cataract": "Orphanet:217049", "Cardiomyopathy - hypotonia - lactic acidosis": "Orphanet:91130", "lung fibroblast": "CL:0002553", "Mazabraud syndrome": "Orphanet:57782", "squamous cell breast carcinoma": "EFO:1000053", "Ectocarpus siliculosus": "NCBITaxon:2880", "Delayed myelination {http": "HP:0012448", "mediastinal cancer": "EFO:0007362", "cardiac amyloidosis": "EFO:1001984", "Conjunctival telangiectasia": "Orphanet:98613", "GM14408 {http": "CLO:0031227", "Poor speech {http": "HP:0002465", "oxalate(1-) {http": "CHEBI:46904", "GM17114 {http": "CLO:0014945", "Agrotis ipsilon": "NCBITaxon:56364", "cytotoxic CD56-dim natural killer cell": "CL:0000939", "fumarate(1-) {http": "CHEBI:37154", "Oxoglutaricaciduria": "Orphanet:31", "GM17173 {http": "CLO:0014026", "Trypanosoma brucei brucei": "NCBITaxon:5702", "plant embryo development stage {http": "PO:0007631", "cervix epithelium": "UBERON:0004801", "water": "CHEBI:15377", "GR 127935 hydrochloride": "CHEBI:64111", "activities of daily living score measurement": "EFO:0008451", "HMEC": "EFO:0001188", "male reproductive system": "UBERON:0000079", "NK1.1-positive natural killer cell": "CL:0002438", "embryonic frontal ganglion": "FBbt:00005668", "abdomen": "UBERON:0000916", "thoracic-to-hip circumference ratio measurement": "EFO:0007769", "GM14481 {http": "CLO:0031533", "mass unit": "UO:0000002", "CD25-positive, CD27-positive immature gamma-delta T cell": "CL:0002126", "Dappled diaphyseal dysplasia": "Orphanet:99645", "suppurative thyroiditis": "EFO:1001431", "alpha-amanitin": "CHEBI:37415", "Autosomal dominant spastic paraplegia type 3": "Orphanet:100984", "trombiculiasis": "EFO:0007526", "sodium butyrate": "CHEBI:64103", "phenacetin": "CHEBI:8050", "Distal trisomy 8q": "Orphanet:96100", "Familial ocular anterior segment mesenchymal dysgenesis": "Orphanet:88632", "forelimb": "UBERON:0002102", "Lissencephaly syndrome, Norman-Roberts type": "Orphanet:89844", "Posterior Leukoencephalopathy Syndrome": "EFO:1001829", "Hereditary sensory and autonomic neuropathy type 7": "Orphanet:391397", "corneal neovascularization": "EFO:1000880", "synthetic DNA data": "EFO:0004604", "abnormality of the integument": "HP:0001574", "tonsillar macrophage": "CL:0000869", "cervical adenocarcinoma": "EFO:0001416", "nandrolone": "CHEBI:7466", "year": "UO:0000036", "Protomelas similis": "NCBITaxon:29149", "Genetic hair anomaly": "Orphanet:183450", "monophasic synovial sarcoma": "EFO:0000595", "Charcot-Marie-Tooth disease type 2B2": "Orphanet:101101", "trichostatin A": "CHEBI:46024", "Isolated focal cortical dysplasia type II": "Orphanet:268994", "Congenital symblepharon": "Orphanet:98948", "Autosomal recessive cutis laxa type 2": "Orphanet:90350", "visceral adipose tissue measurement": "EFO:0004765", "Neurofibromatosis type 3": "Orphanet:93921", "Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency": "Orphanet:404440", "Qualitative or quantitative defects of collagen 6": "Orphanet:207090", "GM17291 {http": "CLO:0013135", "CB4555": "EFO:0004051", "Cardamine sp. SIM-2007": "NCBITaxon:487795", "CB189": "EFO:0004076", "pancreatic somatostatinoma": "EFO:1001964", "ventricular rate measurement": "EFO:0007928", "Wyburn-Mason syndrome": "Orphanet:53719", "amyloid-beta measurement": "EFO:0005194", "Capan1": "EFO:0002153", "Blastocladiella emersonii": "NCBITaxon:4808", "D721Med": "EFO:0005696", "AB SOLiD 5500xl": "EFO:0004436", "Hepatoid Adenocarcinoma": "EFO:1000293", "CD103-negative, langerin-positive lymph node dendritic cell": "CL:0002510", "CS57677": "EFO:0000060", "pharyngula prim-5": "EFO:0001314", "Colorectal Hamartoma": "EFO:1000193", "cicatricial alopecia": "EFO:1002028", "glucuronate {http": "CHEBI:24297", "Bradyopsia": "Orphanet:75374", "musical aptitude": "EFO:0005690", "milk allergy measurement": "EFO:0007019", "Absent speech {http": "HP:0001344", "Proteasome disability syndrome": "Orphanet:324977", "WERI-Rb-1": "EFO:0005715", "Spastic paraplegia": "HP:0001258", "Male infertility due to gonadal dysgenesis": "Orphanet:98313", "Congenital hypothyroidism due to developmental anomaly": "Orphanet:95711", "X-linked intellectual disability, Martinez type": "Orphanet:775", "chloroplast part": "GO:0044434", "Primary hyperoxaluria type 2": "Orphanet:93599", "Salmonella enterica subsp. enterica serovar Muenchen": "NCBITaxon:596", "Bur-0": "EFO:0005170", "Oryza sativa": "NCBITaxon:4530", "Ishikawa": "EFO:0005718", "4-cell embryo Ce": "EFO:0005500", "mouth morphology measurement": "EFO:0007955", "Fuhrmann syndrome": "Orphanet:2854", "Thoracolaryngopelvic dysplasia": "Orphanet:3317", "Congenital sucrase-isomaltase deficiency without sucrose intolerance": "Orphanet:306486", "adipose tissue of abdominal region": "UBERON:0007808", "Collinsella": "NCBITaxon:102106", "pain": "EFO:0003843", "Neurospora tetrasperma": "NCBITaxon:40127", "Ectodermal dysplasia with natal teeth, Turnpenny type": "Orphanet:69083", "Autosomal recessive spastic paraplegia type 32": "Orphanet:171622", "vascular system {http": "PO:0000034", "Neonatal osteosclerotic dysplasia": "Orphanet:93443", "amelanotic melanoma": "EFO:1001937", "ethylene treatment {http": "EO:0007068", "NSAID use measurement": "EFO:0007012", "Hutchinson-Gilford progeria syndrome": "Orphanet:740", "Lethal osteosclerotic bone dysplasia": "Orphanet:1832", "ES-E14 cell": "BTO:0005136", "Transient neonatal multiple acyl-CoA dehydrogenase deficiency": "Orphanet:329942", "Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation": "Orphanet:1970", "Oculopharyngeal muscular dystrophy": "Orphanet:270", "CMK": "EFO:0003037", "gynoecium development stage {http": "PO:0007606", "GM14506 {http": "CLO:0031519", "P wave duration": "EFO:0005094", "hepatocyte growth factor measurement": "EFO:0006903", "Gluconeogenesis disorder": "Orphanet:79177", "activated type II NK T cell": "CL:0000931", "Schwartz-Jampel syndrome": "Orphanet:800", "chemical treatment {http": "EO:0007189", "genotyping by high throughput sequencing": "EFO:0002771", "focal segmental glomerulosclerosis": "EFO:0004236", "Autosomal codominant severe lipodystrophic laminopathy": "Orphanet:280365", "Odontogenic Cyst": "EFO:1000406", "Pyogenic arthritis - pyoderma gangrenosum - acne": "Orphanet:69126", "GM17844 {http": "CLO:0016454", "micromole per kilogram": "EFO:0002900", "Cold-induced sweating syndrome": "Orphanet:157820", "Disorder of lipid metabolism": "Orphanet:309005", "trophozoite": "EFO:0002592", "blast cell": "CL:0000055", "UACC-257": "EFO:0005376", "nanometer": "UO:0000018", "Spondyloepiphyseal dysplasia, Cantu type": "Orphanet:163654", "red color blindness": "EFO:0005580", "Gr1-positive, CD43-positive monocyte": "CL:0002398", "Metabolic disease with intestinal involvement": "Orphanet:104013", "Iniencephaly": "Orphanet:63259", "thymus hyperplasia": "EFO:1001860", "15q13.3 microdeletion syndrome": "Orphanet:199318", "Qualitative or quantitative protein defects in neuromuscular diseases": "Orphanet:207049", "molecular function": "GO:0003674", "Multiple osteochondromas": "Orphanet:321", "hemorrhagic fever with renal syndrome": "EFO:0007299", "Ruvalcaba syndrome": "Orphanet:3121", "susceptibility to hepatitis A infection measurement": "EFO:0008415", "acanthosis nigricans": "EFO:1000660", "Single cell ATAC-seq (cell index)": "EFO:0008925", "Multisystemic smooth muscle dysfunction syndrome": "Orphanet:404463", "7alpha-hydroxy-3-oxo-4-cholestenoic acid {http": "CHEBI:83036", "Trisomy 12p": "Orphanet:1699", "Bilateral conductive hearing impairment {http": "HP:0008513", "population growth assay": "EFO:0002907", "chronic mucus hypersecretion": "EFO:0005673", "fruit size 70% to final size stage {http": "PO:0025508", "Gonosome anomaly": "Orphanet:98155", "ribonucleoside monophosphate biosynthetic process": "GO:0009156", "Feingold syndrome type 2": "Orphanet:391646", "Fragaria x ananassa": "NCBITaxon:3747", "AA120": "EFO:0004072", "torus semicircularis": "UBERON:2000599", "Spinal Osteochondrosis": "EFO:0008576", "Megalencephalic leukoencephalopathy with subcortical cysts": "Orphanet:2478", "Diffuse mesangial sclerosis {http": "HP:0001967", "Fraction D precursor B cell": "CL:0002052", "Combined immunodeficiency due to CRAC channel dysfunction": "Orphanet:169090", "Haemophilus ducreyi 35000HP": "NCBITaxon:233412", "bacterial thylakoid": "GO:0030075", "Appendix Hyperplastic Polyp": "EFO:1000091", "Suarez-Stickler syndrome": "Orphanet:166277", "Lymphoma, AIDS-Related": "EFO:1001365", "enterotoxemia": "EFO:1000922", "substernal goiter": "EFO:1001198", "polysaccharide": "CHEBI:18154", "lung adenocarcinoma": "EFO:0000571", "leukostasis": "EFO:1001016", "nitrocellulose substrate": "EFO:0005064", "Rare genetic disease with myoclonus as a major feature": "Orphanet:307067", "sebaceous of Jadassohn nevus": "EFO:1001841", "male reproductive organ cancer": "EFO:0007355", "Psoas abscess": "EFO:1001832", "Dictyostelium purpureum": "NCBITaxon:5786", "endothelial dysfunction": "EFO:1001461", "CAL62": "EFO:0002126", "influenza A (H1N1)": "EFO:1001488", "Congenital lobar emphysema": "Orphanet:1928", "Glutathione synthetase deficiency": "Orphanet:32", "ILSXISS66/TejJ": "EFO:0002991", "brain stem neoplasm": "EFO:1001767", "chemotherapy-induced hypertension": "EFO:0005942", "lipoatrophic diabetes": "EFO:0007346", "lysine": "CHEBI:25094", "T98G": "EFO:0002085", "NCI-H1623": "EFO:0002259", "pelvic fin": "UBERON:0000152", "Metaphyseal chondrodysplasia, Jansen type": "Orphanet:33067", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B": "Orphanet:308393", "HCC2270": "EFO:0006430", "iPS-17a": "EFO:0007103", "response to vaccine": "EFO:0004645", "X-linked intellectual disability, Porteous type": "Orphanet:93945", "legionellosis": "EFO:0007342", "protein glycosylation in endoplasmic reticulum": "GO:0033577", "IgD-negative CD38-positive IgG memory B cell": "CL:0002107", "SW756": "EFO:0002370", "Synechocystis sp. PCC 6803": "NCBITaxon:1148", "response to buspirone": "EFO:0006330", "plasmatocyte": "FBbt:00001685", "Glycine max cv. Williams 82.": "EFO:0007023", "Intermediate maple syrup urine disease": "Orphanet:268162", "Salmo trutta": "NCBITaxon:8032", "Unclassified intestinal pseudoobstruction": "Orphanet:104078", "NCI-H2170": "EFO:0002281", "rheumatoid factor measurement": "EFO:0005767", "coronary artery raised atherosclerotic lesion": "EFO:0005616", "B-Cell Prolymphocytic Leukemia": "EFO:1000102", "Hematuria {http": "HP:0000790", "Ossifying Fibromyxoid Tumor": "EFO:1000408", "Waddling gait {http": "HP:0002515", "Mononegavirales infectious disease": "EFO:0007376", "46,XY disorder of sex development due to testicular steroidogenesis defect": "Orphanet:90787", "N-formyl-L-methionine {http": "CHEBI:16552", "Iridovirus": "NCBITaxon:10487", "heavy metal poisoning": "EFO:1001518", "whole plant flowering stage": "PO:0007016", "Combined malonic and methylmalonic acidemia": "Orphanet:289504", "Congenital sucrase-isomaltase deficiency with minimal starch tolerance": "Orphanet:306446", "Guillain-Barre syndrome": "EFO:0007292", "middle cerebral artery infarction": "EFO:1001045", "Ara-C-sensitive parental cell line": "EFO:0002033", "drug-induced agranulocytosis": "HP:0012235", "SU.86.86": "EFO:0006494", "Carpotarsal osteochondromatosis": "Orphanet:2767", "Ring chromosome 1": "Orphanet:1437", "pleural macrophage": "CL:0002247", "Dehydrated hereditary stomatocytosis": "Orphanet:3202", "LP.08 eight leaves visible stage": "PO:0007095", "erythroblast": "CL:0000765", "1-stearoyl-sn-glycero-3-phosphocholine {http": "CHEBI:73858", "heterogeneous": "HP:0001425", "osteoarthritis": "EFO:0002506", "NCI-H2803": "EFO:0006687", "GM17129 {http": "CLO:0015130", "Jawad syndrome": "Orphanet:313795", "Gnathodiaphyseal dysplasia": "Orphanet:53697", "Dysphagia": "HP:0002015", "Autosomal recessive isolated optic atrophy": "Orphanet:98676", "malaria": "EFO:0001068", "Euphausia superba": "NCBITaxon:6819", "viral pneumonia": "EFO:0007541", "neurogenic bowel": "EFO:1001061", "erythropoietin": "EFO:0003233", "epididymis": "UBERON:0001301", "Kinetic eyelid anomaly": "Orphanet:98577", "Fundus pulverulentus": "Orphanet:99004", "cervicofacial actinomycosis": "EFO:0007203", "animal reproductive system cell": "EFO:0002962", "EM2": "EFO:0002176", "acquired long QT syndrome": "EFO:0005138", "Cryptogenic Organizing Pneumonia": "EFO:1001300", "glass substrate": "EFO:0005062", "Bladder Adenocarcinoma": "EFO:1000125", "illuminance unit": "UO:0000115", "internal carotid intimal medial thickness": "EFO:0005053", "Benign essential blepharospasm": "Orphanet:93955", "Hepatoblastoma": "EFO:1000292", "arachidonic acid measurement": "EFO:0006808", "ML-DmD32": "EFO:0005830", "Hereditary motor and sensory neuropathy type 5": "Orphanet:64751", "plasminogen activator inhibitor 1 measurement": "EFO:0004792", "Schrenkiella parvula {http": "NCBITaxon:98039", "Rhizomelic chondrodysplasia punctata type 2": "Orphanet:309796", "CS57627": "EFO:0000043", "neurally mediated hypotension": "EFO:0005254", "CS57572": "EFO:0000019", "Glycerol kinase deficiency": "Orphanet:308993", "all-cis-docosa-4,7,10,13,16,19-hexaenoic acid": "CHEBI:28125", "bronchopneumonia": "EFO:0007184", "Multiple carboxylase deficiency": "Orphanet:148", "Hemangioma, Cavernous, Central Nervous System": "EFO:1001343", "Human adenovirus 7": "NCBITaxon:10519", "Muscle filaminopathy": "Orphanet:171445", "aggressive periodontitis": "EFO:0006342", "Inherited giant platelet disorder": "Orphanet:220452", "Mus musculus strain type": "EFO:0004000", "INSeq": "EFO:0008782", "Illumina HiSeq 2000": "EFO:0004203", "Duchenne and Becker muscular dystrophy": "Orphanet:262", "Familial avascular necrosis of femoral head": "Orphanet:86820", "Galactosialidosis": "Orphanet:351", "Hyperkalemic periodic paralysis": "Orphanet:682", "dysplastic nevus": "EFO:0004199", "C-C motif chemokine 14 measurement": "EFO:0008042", "G1E": "EFO:0002034", "rosuvastatin": "CHEBI:38545", "Selective pituitary resistance to thyroid hormone": "Orphanet:165994", "pyruvate {http": "CHEBI:15361", "Mild Canavan disease": "Orphanet:314918", "FAIRE-seq": "EFO:0004428", "tag based single cell RNA sequencing": "EFO:0008440", "Infantile convulsions and choreoathetosis": "Orphanet:31709", "Pelviscapular dysplasia": "Orphanet:93333", "allergic contact dermatitis": "EFO:1000668", "Atrioventricular defect - blepharophimosis -radial defects": "Orphanet:1352", "Abnormality of blood glucose concentration": "HP:0011015", "HepG3": "EFO:0005382", "RPMI-7951": "EFO:0005712", "LP.10 ten leaves visible stage": "PO:0007103", "Microvillus inclusion disease": "Orphanet:2290", "3-aminophenol": "CHEBI:28924", "Atypical hemolytic-uremic syndrome": "Orphanet:2134", "cyclosporin A": "CHEBI:4031", "cognitive decline measurement": "EFO:0007710", "intracranial hemorrhage NOS": "EFO:0000551", "cocaine dependence": "EFO:0002610", "Prader-Willi-like syndrome due to point mutation": "Orphanet:398079", "Familial atrial myxoma": "Orphanet:615", "DN2b thymocyte": "CL:0002424", "Neisseria mucosa": "NCBITaxon:488", "Niemann-Pick disease type A": "Orphanet:77292", "Xanthomonas translucens pv. cerealis {http": "NCBITaxon:152263", "ATC Code S Sensory organs": "EFO:0005646", "Salmonella enterica subsp. enterica serovar Typhisuis": "NCBITaxon:41529", "Dermacentor andersoni": "NCBITaxon:34620", "GM17808 {http": "CLO:0016504", "chromosome-defective micronuclei": "EFO:1001778", "Verloove Vanhorick-Brubakk syndrome": "Orphanet:3429", "X-linked intellectual disability - cardiomegaly - congestive heart failure": "Orphanet:324410", "SNB19": "EFO:0002342", "Monosomy 18p": "Orphanet:1598", "Charcot-Marie-Tooth disease type 4F": "Orphanet:99952", "Simple Endometrial Hyperplasia": "EFO:1000525", "Pantothenate kinase-associated neurodegeneration": "Orphanet:157850", "GM17737 {http": "CLO:0017044", "Disorder of thiamine metabolism and transport": "Orphanet:298644", "waist circumference": "EFO:0004342", "Polysyndactyly": "Orphanet:93338", "fludarabine phosphate": "CHEBI:63599", "Syndactyly type 2": "Orphanet:93403", "Streptomyces coelicolor": "NCBITaxon:1902", "response to triptolide": "EFO:0007662", "Saccharopolyspora erythraea": "NCBITaxon:1836", "Juvenile polyposis of infancy": "Orphanet:79076", "Autosomal recessive spastic paraplegia type 45": "Orphanet:320396", "Male infertility due to globozoospermia": "Orphanet:171709", "intestinal cancer": "EFO:0007330", "GM12006": "EFO:0001131", "Disorder of lysine and hydroxylysine metabolism": "Orphanet:289832", "SMiLE-seq": "EFO:0008933", "Metarhizium anisopliae": "NCBITaxon:5530", "Familial infantile gigantism": "Orphanet:300373", "Craniosynostosis - hydrocephalus - Arnold-Chiari malformation type I - radioulnar synostosis": "Orphanet:171839", "collecting duct carcinoma": "EFO:0003016", "Ermine phenotype": "Orphanet:999", "paracoccidioidomycosis": "EFO:0007417", "Catania ecotype": "EFO:0006981", "Bru-Seq": "EFO:0008661", "chorion": "UBERON:0003124", "Renal tubulopathy - encephalopathy - liver failure": "Orphanet:254902", "increased concentration": "PATO:0001162", "MDAMB134VI": "EFO:0001205", "phlegm": "UBERON:0016552", "factor VIII deficiency": "EFO:0007267", "short term hematopoietic stem cell": "CL:0002033", "chlorpromazine": "CHEBI:3647", "erythropoetin measurement": "EFO:0008391", "Saccharomyces pastorianus Weihenstephan 34/70": "NCBITaxon:520522", "Genetic progeroid syndrome": "Orphanet:363245", "response to phenytoin": "EFO:0006345", "OSLAM syndrome": "Orphanet:2760", "experimental autoimmune encephalomyelitis": "EFO:0001066", "Lethal congenital contracture syndrome type 1": "Orphanet:1486", "GM17215 {http": "CLO:0013885", "GM17120 {http": "CLO:0015112", "thymic medullary macrophage": "CL:0000882", "antiviral": "CHEBI:22587", "pantothenate {http": "CHEBI:16454", "Autosomal recessive spastic ataxia - optic atrophy - dysarthria": "Orphanet:254343", "congenital fibrosis of the extraocular musclesCongenital fibrosis of extraocular muscles": "EFO:1001985", "Brugada syndrome": "Orphanet:130", "SMORE-Seq": "EFO:0008936", "Leukoencephalopathy-palmoplantar keratoderma syndrome": "Orphanet:2386", "HapMap haplotype mapping": "EFO:0002924", "Syndromic cataract": "Orphanet:98641", "Anomaly of puberty or/and menstrual cycle of genetic origin": "Orphanet:202940", "Po-0": "EFO:0006972", "Zea mays subsp. mexicana {http": "NCBITaxon:4579", "Angioosteohypertrophic syndrome": "Orphanet:2346", "proprotein convertase subtilisin/kexin type 7 measurement": "EFO:0008270", "scopolamine methobromide": "CHEBI:61276", "Carnitine palmitoyl transferase II deficiency, myopathic form": "Orphanet:228302", "Erwinia amylovora": "NCBITaxon:552", "scimitar syndrome": "EFO:1001167", "Crassostrea virginica": "NCBITaxon:6565", "Bile acid CoA ligase deficiency and defective amidation": "Orphanet:276066", "coronary heart disease": "EFO:0001645", "oxidised LDL": "CHEBI:60151", "RBNS": "EFO:0008884", "Cordyceps militaris": "NCBITaxon:73501", "array data file": "EFO:0004098", "Mus musculus": "NCBITaxon:10090", "Acanthamoeba keratitis": "EFO:0007126", "growth condition": "EFO:0000523", "Alexa Fluor 647": "EFO:0004967", "Hb Bart's hydrops fetalis": "Orphanet:163596", "organelle envelope": "GO:0031967", "nucleotide biosynthetic process": "GO:0009165", "Usher syndrome": "Orphanet:886", "SH4": "EFO:0002327", "cycloheximide": "CHEBI:27641", "Pyro-L-glutaminyl-L-glutamine {http": "CHEBI:88956", "Microblepharon - ablephara": "Orphanet:98563", "piperine {http": "CHEBI:28821", "2-hydroxyglutarate(1-) {http": "CHEBI:36149", "skin tags": "HP:0010609", "Joubert syndrome with oculorenal defect": "Orphanet:2318", "CAMA1": "EFO:0001100", "Burren ecotype": "EFO:0005169", "Hemiparkinsonism-hemiatrophy syndrome": "Orphanet:306669", "Taraxacum officinale": "NCBITaxon:50225", "chromophobe renal cell carcinoma": "EFO:0000335", "Chronic Eosinophilic Leukemia, Not Otherwise Specified": "EFO:1000178", "Intimal Sarcoma": "EFO:1000305", "North Carolina macular dystrophy": "Orphanet:75327", "X-linked intellectual disability - ataxia - apraxia": "Orphanet:85338", "sNuc-Seq": "EFO:0008941", "3-O-methyldopa {http": "CHEBI:82913", "plasma beta-amyloid 1-40 measurement": "EFO:0005659", "Hereditary breast and ovarian cancer syndrome": "Orphanet:145", "replicate": "EFO:0000683", "Hereditary spherocytosis": "Orphanet:822", "Purine nucleoside phosphorylase deficiency": "Orphanet:760", "Pseudodiastrophic dysplasia": "Orphanet:85174", "X-linked Emery-Dreifuss muscular dystrophy": "Orphanet:98863", "Populus trichocarpa x Populus deltoides": "NCBITaxon:3695", "Brain calcification, Rajab type": "Orphanet:178506", "CD109 antigen measurement": "EFO:0008076", "subcutaneous adipose tissue measurement": "EFO:0004766", "febrile seizures": "HP:0002373", "Global developmental delay - osteopenia - ectodermal defect": "Orphanet:73223", "vesicoureteral reflux": "EFO:0007536", "Thermotoga maritima": "NCBITaxon:2336", "Pseudomonas aeruginosa UCBPP-PA14": "NCBITaxon:208963", "interleukin-26 (Homo sapiens)": "EFO:0003806", "Aminoacylase deficiency": "Orphanet:308448", "cellular process": "GO:0009987", "MDAMB435": "EFO:0001213", "Borderline Ovarian Serous Tumor": "EFO:1000139", "germ cell": "CL:0000586", "border disease": "EFO:0007177", "Synechococcus sp. CC9311": "NCBITaxon:64471", "Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria": "Orphanet:1035", "CD4-positive, CD25-positive, alpha-beta regulatory T cell": "CL:0000792", "malacoplakia": "EFO:1001807", "seqFISH": "EFO:0008991", "Streptococcus infantis": "NCBITaxon:68892", "lipid": "CHEBI:18059", "colorectal cancer cell line": "BTO:0001616", "organelle membrane": "GO:0031090", "exploratory eye movement measurement": "EFO:0007700", "Chylomicron retention disease": "Orphanet:71", "Familial tumoral calcinosis": "Orphanet:306661", "choroid plexus cancer": "EFO:0007206", "Proximal spinal muscular atrophy": "Orphanet:70", "Splenic Diffuse Large B-Cell Lymphoma": "EFO:1000547", "Brachydactyly of fingers, unilateral": "Orphanet:295128", "folic acid transporter activity": "GO:0008517", "kernicterus": "EFO:1001002", "CAL54": "EFO:0002125", "Bloch-Sulzberger syndrome": "EFO:1000672", "Dentin dysplasia": "Orphanet:1653", "9,10-DiHOME {http": "CHEBI:72663", "GM17168 {http": "CLO:0013987", "gout": "EFO:0004274", "response to aromatase inhibitor": "GO:0061477", "Macrocephaly - spastic paraplegia - dysmorphism": "Orphanet:2429", "Multiple cafe-au-lait spots {http": "HP:0007565", "Czech dysplasia, metatarsal type": "Orphanet:137678", "Autosomal recessive spastic paraplegia type 59": "Orphanet:401795", "ILSXISS25/TejJ": "EFO:0002981", "carboxypeptidase B2 measurement": "EFO:0008069", "SK-MEL-2": "EFO:0002079", "cytokine role": "EFO:0003787", "baicalin": "CHEBI:2981", "Grayson-Wilbrandt corneal dystrophy": "Orphanet:293375", "GM12763": "EFO:0001154", "swine influenza": "EFO:0005226", "hermaphrodite": "PATO:0001340", "Metallosphaera sedula": "NCBITaxon:43687", "Fatal infantile hypertonic myofibrillar myopathy": "Orphanet:280553", "Distal trisomy 2q": "Orphanet:96094", "polyploid {http": "PATO:0001377", "ML2": "EFO:0002238", "NT-1": "EFO:0002707", "GM11994": "EFO:0001126", "gamma-CEHC {http": "CHEBI:89379", "bronchoalveolar lavage": "BTO:0000155", "response to lapatinib": "GO:0036274", "coronary artery bypass": "EFO:0003776", "2-linoleoyl-sn-glycero-3-phosphoethanolamine {http": "CHEBI:76233", "germplasm": "EFO:0007059", "angiogenin measurement": "EFO:0008022", "root caries": "EFO:1001163", "low fat diet": "EFO:0002758", "Spondylocostal dysostosis - anal and genitourinary malformations": "Orphanet:94095", "nevirapine": "CHEBI:63613", "Familial primary hyperparathyroidism": "Orphanet:2207", "posterior lateral mesoderm": "ZFA:0005040", "wet macular degeneration": "EFO:0004683", "Hereditary fructose intolerance": "Orphanet:469", "lingual goiter": "EFO:1001018", "B117H": "EFO:0002040", "Bla-1": "EFO:0005167", "interferon gamma measurement": "EFO:0008165", "gas gangrene": "EFO:0007279", "cutaneous syphilis": "EFO:1000887", "Eyebrow/eyelashes distichiasis": "Orphanet:98600", "suicide": "EFO:0007624", "Amniotic bands": "Orphanet:1034", "single cell sequencing": "EFO:0007832", "CRE-Seq": "EFO:0008699", "Peutz-Jeghers syndrome": "Orphanet:2869", "C4II": "EFO:0002123", "mass spectrometer": "OBI:0000049", "Pancreatic colipase deficiency": "Orphanet:309108", "small cell lung carcinoma": "EFO:0000702", "medial nasal prominence {http": "UBERON:0004068", "myeloblast": "CL:0000835", "20p12.3 microdeletion syndrome": "Orphanet:261295", "benzylpenicillin": "CHEBI:18208", "response to nitrofurantoin": "EFO:0007921", "sonicator": "OBI:0400114", "Non-Neoplastic Bile Duct Disorder": "EFO:1000400", "A427": "EFO:0002104", "Distal 17p13.1 microdeletion syndrome": "Orphanet:319171", "Attenuated familial adenomatous polyposis": "Orphanet:220460", "intracranial arterial disease": "EFO:1000990", "acyclovir": "CHEBI:2453", "Glycogen storage disease due to acid maltase deficiency": "Orphanet:365", "periodic limb movement disorder": "EFO:0007428", "Severe combined immunodeficiency due to IKK2 deficiency": "Orphanet:397787", "methylation profiling by high throughput sequencing": "EFO:0002761", "Autosomal dominant cervical dystonia": "Orphanet:93962", "antioxidant measurement": "EFO:0005119", "BMI-adjusted waist-hip ratio": "EFO:0007788", "Pseudohyperaldosteronism type 2": "Orphanet:88660", "SNU-C1": "EFO:0006761", "fibroepithelial polyp of urethra": "EFO:1000700", "breastfeeding duration": "EFO:0006864", "Systemic capillary leak syndrome": "EFO:1001477", "Illumina native fastq format": "EFO:0004166", "cholesterol embolism": "EFO:0005801", "Hereditary cerebral hemorrhage with amyloidosis, Italian type": "Orphanet:324713", "NF90-8": "EFO:0006288", "root cortex": "PO:0000258", "Cycas rumphii": "NCBITaxon:58031", "chickenpox": "EFO:0007204", "femtoliter": "UO:0000104", "stag1-related disorder": "EFO:0009078", "type I diabetes mellitus": "EFO:0001359", "Flavivirus Infections": "EFO:1001326", "SPONASTRIME dysplasia": "Orphanet:93357", "Central cloudy dystrophy of Francois": "Orphanet:98972", "dehydroepiandrosterone sulfate": "CHEBI:16814", "624 mel": "EFO:0006359", "Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan": "Orphanet:207113", "Proximal spinal muscular atrophy type 3": "Orphanet:83419", "CHIME syndrome": "Orphanet:3474", "Autosomal recessive Robinow syndrome": "Orphanet:1507", "annexin A1 measurement": "EFO:0008026", "Spastic ataxia with congenital miosis": "Orphanet:1182", "Lysosomal disease": "Orphanet:68366", "Acromelic frontonasal dysplasia": "Orphanet:1827", "Lactobacillus alimentarius": "NCBITaxon:1602", "Phakomatosis cesiomarmorata": "Orphanet:79484", "millimeter": "UO:0000016", "HUES44": "EFO:0007081", "Salmonella enterica subsp. enterica serovar Infantis": "NCBITaxon:595", "Rare genetic intellectual disability with developmental anomaly": "Orphanet:183763", "Classic maple syrup urine disease": "Orphanet:268145", "calyx development stage {http": "PO:0007603", "primitive erythroid lineage cell": "CL:0002417", "ATC Code V Various": "EFO:0005647", "jasmonic acid": "CHEBI:18292", "microscopic polyangiitis": "EFO:1000784", "Disorder of protein N-glycosylation": "Orphanet:309347", "nectar": "EFO:0001046", "Corynebacterium diphtheriae": "NCBITaxon:1717", "Nephrogenic rest": "HP:0100880", "Wilson disease": "Orphanet:905", "spike-in quality control role": "OBI:0001140", "Erythrokeratoderma \\\"en cocardes\\\"": "Orphanet:315", "Moniezia expansa": "NCBITaxon:28841", "Weissenbacher- Zweymuller syndrome": "Orphanet:3450", "Amelia of upper limb": "Orphanet:294967", "Spinocerebellar ataxia type 21": "Orphanet:98773", "glioma": "EFO:0005543", "chronic hepatitis B infection": "EFO:0004239", "Ehrlichia chaffeensis str. Arkansas": "NCBITaxon:205920", "Mixed sclerosing bone dystrophy with extra-skeletal manifestations": "Orphanet:324364", "Ciona intestinalis": "NCBITaxon:7719", "CD8-positive, alpha-beta cytokine secreting effector T cell": "CL:0000908", "293T": "EFO:0001082", "Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence": "Orphanet:3201", "CS57549": "EFO:0000012", "dalton": "UO:0000221", "tumor mass": "EFO:0007062", "Isolated succinate-CoQ reductase deficiency": "Orphanet:3208", "inclusive hindgut primordium": "FBbt:00005523", "Trisomy 1q": "Orphanet:261344", "RepeatSeq": "EFO:0008888", "Trichodental syndrome": "Orphanet:3351", "amygdala volume": "EFO:0006934", "NPC": "EFO:0004041", "K562": "EFO:0002067", "Leigh syndrome": "Orphanet:506", "PK-45H": "EFO:0006734", "Episodic ataxia type 7": "Orphanet:209970", "chloroplast": "GO:0009507", "Punctate cataract": "HP:0007648", "Axial mesodermal dysplasia spectrum": "Orphanet:1834", "Hereditary motor and sensory neuropathy, Okinawa type": "Orphanet:90117", "Oculo-palato-cerebral syndrome": "Orphanet:2714", "osteonecrosis": "EFO:0004259", "Laron syndrome": "Orphanet:633", "Chikungunya encephalitis": "EFO:0008494", "C170": "EFO:0006363", "Split hand, unilateral": "Orphanet:295120", "Delayed speech - facial asymmetry - strabismus - ear lobe creases": "Orphanet:3038", "Ovarian Microcystic Stromal Tumor": "EFO:1000424", "Aedes aegypti": "NCBITaxon:7159", "coronary artery disease": "EFO:0000378", "anti-Heliobacter pylori serum IgG measurement": "EFO:0005247", "mucoepidermoid tumor": "EFO:1001049", "heart disease": "EFO:0003777", "fCAB-Seq": "EFO:0008741", "E-YSL": "UBERON:2000309", "gentamicin": "CHEBI:17833", "Partial deletion of chromosome 17": "Orphanet:261831", "2-nitrofluorene": "CHEBI:1224", "Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome": "Orphanet:306504", "Chondrodysplasia with joint dislocations, gPAPP type": "Orphanet:280586", "Distal symphalangism": "Orphanet:3248", "dinitrophenol": "CHEBI:39352", "Thiamine-responsive megaloblastic anemia syndrome": "Orphanet:49827", "Vigna unguiculata": "NCBITaxon:3917", "Dysplastic cortical hyperostosis": "Orphanet:2204", "LOXIMVI": "EFO:0006284", "Fabry disease": "Orphanet:324", "verbal-numerical reasoning measurement": "EFO:0008394", "Hereditary acrokeratotic poikiloderma, Weary type": "Orphanet:2907", "Congenital vitreoretinal dysplasia": "Orphanet:98669", "LXF-289": "EFO:0006641", "HUES45": "EFO:0007082", "Anomaly of the secretory and excretory apparatus of the lacrimal system": "Orphanet:98608", "embryonic esophagus": "FBbt:00005612", "Hantavirus infectious disease": "EFO:0007295", "MELAS": "Orphanet:550", "Macrocephaly {http": "HP:0000256", "Lipomyelomeningocele": "Orphanet:268835", "kernicterus due to isoimmunization": "EFO:1000721", "IgG index": "EFO:0006929", "Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies": "Orphanet:98370", "gonad primordium": "UBERON:0005564", "Zymomonas mobilis": "NCBITaxon:542", "Fundulus heteroclitus": "NCBITaxon:8078", "abdominal pain": "HP:0002027", "Abnormal jaw morphology": "HP:0030791", "Malformation syndrome with hamartosis": "Orphanet:98196", "PC12": "EFO:0001225", "Familial isolated dilated cardiomyopathy": "Orphanet:154", "iris": "UBERON:0001769", "Genetic endocrine tumor": "Orphanet:271847", "placenta": "UBERON:0001987", "SNU449": "EFO:0002349", "5-dodecenoate {http": "CHEBI:83046", "Isolated ATP synthase deficiency": "Orphanet:254913", "hexanoate {http": "CHEBI:17120", "Streptomyces griseus": "NCBITaxon:1911", "milligram per kilogram per day": "EFO:0002930", "Col-2": "EFO:0005150", "Jacobsen syndrome": "Orphanet:2308", "Congenital disorder of glycosylation with hepatic involvement": "Orphanet:371157", "mitral annular calcification": "EFO:0005262", "SCC-25": "EFO:0006483", "main bronchus": "UBERON:0002182", "Hypermethioninemia encephalopathy due to adenosine kinase deficiency": "Orphanet:289290", "Muscular dystrophy, Selcen type": "Orphanet:199340", "Primary congenital hypothyroidism": "Orphanet:226295", "Myasthenia gravis": "EFO:0004991", "Syndromic optic nerve hypoplasia": "Orphanet:137905", "MHC-II-low non-classical monocyte": "CL:0002472", "Dyschromatosis universalis": "Orphanet:241", "antipsychotic drug related weight gain": "EFO:0004567", "diaphysis of femur {http": "UBERON:0006862", "T1 tumor stage": "EFO:0004938", "data item": "IAO:0000027", "larval protruding mouth": "EFO:0007696", "Macaca fascicularis": "NCBITaxon:9541", "ND02852 {http": "CLO:0015209", "Candidatus Phytoplasma asteris": "NCBITaxon:85620", "RAVINE syndrome": "Orphanet:99852", "Renal cyst {http": "HP:0000107", "Susceptibility to viral and mycobacterial infections": "Orphanet:391311", "HCC1806": "EFO:0005373", "Isolated trigonocephaly": "Orphanet:3366", "Mucopolysaccharidosis type 2, severe form": "Orphanet:217085", "tooth agenesis": "EFO:0005410", "Burkholderia cepacia": "NCBITaxon:292", "cellular localization": "GO:0051641", "pectoral fin bud": "ZFA:0000141", "CD4-positive helper T cell": "CL:0000492", "otolith organ": "UBERON:0002518", "ranitidine": "CHEBI:8776", "Spinocerebellar ataxia type 26": "Orphanet:101112", "Disorder of amino acid and other organic acid metabolism": "Orphanet:79062", "mild heart failure": "EFO:0003147", "Hypogonadism - mitral valve prolapse - intellectual disability": "Orphanet:2233", "fruit ripening stage": "PO:0025502", "seedhead": "EFO:0001039", "Partial duplication of the short arm of chromosome 11": "Orphanet:262785", "GM17225 {http": "CLO:0014371", "Streptococcus pneumoniae R6": "NCBITaxon:171101", "lobomycosis": "EFO:1001805", "Submandibular Gland Adenoid Cystic Carcinoma": "EFO:1000555", "refractory anemia with ringed sideroblasts": "EFO:0003812", "G96": "EFO:0006412", "collection of material": "EFO:0005066", "Autosomal recessive spastic ataxia with leukoencephalopathy": "Orphanet:314603", "uncultured Acidobacteria bacterium": "NCBITaxon:171953", "HCC1187": "EFO:0001170", "Isolated cytochrome C oxidase deficiency": "Orphanet:254905", "eosinophilic myelocyte": "CL:0000612", "GM1 gangliosidosis type 1": "Orphanet:79255", "input DNA": "EFO:0005031", "organelle part": "GO:0044422", "Kupffer cell": "CL:0000091", "neurogenic arthropathy": "EFO:1001378", "snmC-seq": "EFO:0008939", "GM17265 {http": "CLO:0013163", "Disorders of vitamin D metabolism": "Orphanet:289098", "Pacman dysplasia": "Orphanet:1952", "Autosomal recessive spastic paraplegia type 18": "Orphanet:209951", "Ataxia - pancytopenia": "Orphanet:2585", "trifluoperazine": "CHEBI:45951", "glutamine": "CHEBI:28300", "Isolated cloverleaf skull syndrome": "Orphanet:2343", "Malpighian tubule primordium": "FBbt:00000442", "X-linked intellectual disability due to GRIA3 anomalies": "Orphanet:364028", "Lethal polymalformative syndrome, Boissel type": "Orphanet:210144", "Cocos nucifera": "NCBITaxon:13894", "eyelid neoplasm": "EFO:1000934", "microphthalmia": "EFO:0005569", "Oryctolagus cuniculus": "NCBITaxon:9986", "Isolated oxycephaly": "Orphanet:63440", "BAP1-related tumor predisposition syndrome": "Orphanet:289539", "response to stimulus": "GO:0050896", "Raji": "EFO:0002324", "Eurotium chevalieri": "NCBITaxon:41411", "gamma-Glu-Met {http": "CHEBI:82965", "booting stage {http": "PO:0007014", "fluoxetine": "CHEBI:5118", "oral mucositis": "EFO:1001904", "Unclassified Renal Cell Carcinoma": "EFO:1000603", "HCC0060": "EFO:0006418", "rectum cancer": "EFO:1000657", "uveal cancer": "EFO:1001230", "transcription profiling by SAGE": "EFO:0002941", "GM17798 {http": "CLO:0016489", "CA3 field of hippocampus {http": "UBERON:0003883", "CD27-high, CD11b-low natural killer cell": "CL:0002349", "Hereditary combined deficiency of vitamin K-dependent clotting factors": "Orphanet:98434", "Drosophila simulans": "NCBITaxon:7240", "Familial steroid-resistant nephrotic syndrome with sensorineural deafness": "Orphanet:280406", "Genetic malformation syndrome with short stature": "Orphanet:183570", "Nasu-Hakola disease": "Orphanet:2770", "aromatase inhibitor": "CHEBI:50790", "Hyperammonemia {http": "HP:0001987", "cholesterol homeostasis": "EFO:0005879", "Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract": "Orphanet:171848", "invasive lobular carcinoma": "EFO:0000553", "HEp-2": "EFO:0006438", "ATAC-seq": "EFO:0007045", "HCC1954": "EFO:0001175", "Palpebral sebaceous gland tumor": "Orphanet:98585", "methylmalonic aciduria (cobalamin deficiency) cblA type": "EFO:0009073", "Poecilia reticulata": "NCBITaxon:8081", "ribose phosphate biosynthetic process": "GO:0046390", "grey matter volume measurement": "EFO:0005420", "ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder": "Orphanet:404448", "ILSXISS115/TejJ": "EFO:0003009", "glycerate {http": "CHEBI:33871", "Be cell": "CL:0000968", "pigment": "CHEBI:26130", "Hereditary chronic pancreatitis": "Orphanet:676", "Autosomal dominant spastic paraplegia type 13": "Orphanet:100994", "Arteritis": "EFO:0009011", "oxamic acid": "CHEBI:18058", "neuroendocrine neoplasm": "EFO:1001901", "tooth 4V": "UBERON:2001143", "vulvovaginal candidiasis": "EFO:0007543", "allopurinol": "CHEBI:40279", "Double uterus - hemivagina - renal agenesis": "Orphanet:3411", "potassium": "CHEBI:26216", "SKUT1": "EFO:0002341", "Mint-ChIP": "EFO:0008813", "lipid metabolic process": "GO:0006629", "neuroaspergillosis": "EFO:0007393", "ring gland primordium": "FBbt:00017009", "Myoclonic epilepsy of infancy": "Orphanet:86909", "sensory nervous system primordium": "FBbt:00005551", "NCI-H2279": "EFO:0003120", "Pseudomonas syringae pv. japonica {http": "NCBITaxon:199200", "Non-syndromic polydactyly, syndactyly and/or hyperphalangy": "Orphanet:93458", "X-linked Charcot-Marie-Tooth disease type 2": "Orphanet:101076", "GM17216 {http": "CLO:0013888", "radiologic finding": "EFO:0006887", "visual primordium": "UBERON:6001059", "estradiol measurement": "EFO:0004697", "Autosomal recessive spastic paraplegia type 26": "Orphanet:101006", "Diffuse palmoplantar keratoderma": "Orphanet:307141", "Mycobacterium smegmatis str. MC2 155": "NCBITaxon:246196", "glomerular filtration rate": "EFO:0005208", "Spinocerebellar ataxia type 35": "Orphanet:276193", "Oley syndrome": "Orphanet:79458", "linguistic error measurement": "EFO:0007798", "Salmonella enterica subsp. enterica serovar Choleraesuis": "NCBITaxon:119912", "Vgamma5-positive CD8alpha alpha positive gamma-delta intraepithelial T cell": "CL:0002513", "CS57637": "EFO:0000048", "thyrocyte": "EFO:0003076", "Sialidosis type 2": "Orphanet:87876", "follicular thyroid carcinoma": "EFO:0000501", "HCC4011": "EFO:0006436", "CD11b-positive, CD27-positive natural killer cell": "CL:0002426", "Congenital factor VII deficiency": "Orphanet:327", "2,3-dihydroxy-3-methylbutanoate {http": "CHEBI:11424", "CS57770": "EFO:0000111", "COV362": "EFO:0006383", "Aromatic L-amino acid decarboxylase deficiency": "Orphanet:35708", "TARDIS": "EFO:0008962", "Drosophila sechellia x Drosophila simulans": "NCBITaxon:380737", "respiratory quotient": "EFO:0005189", "plasmacytoma": "EFO:0006738", "erucic acid measurement": "EFO:0007976", "ezRAD": "EFO:0008734", "Qualitative or quantitative defects of alphaB-cristallin": "Orphanet:209044", "CD1a-positive Langerhans cell": "CL:0001014", "congenital nystagmus": "EFO:0007217", "GM17775 {http": "CLO:0016638", "picomolar": "UO:0000066", "Ovarian Mixed Epithelial Tumor": "EFO:1000425", "Hypospadias - intellectual disability, Goldblatt type": "Orphanet:2261", "Ovarian Sclerosing Stromal Tumor": "EFO:1000426", "brain measurement": "EFO:0004464", "KP-2": "EFO:0006621", "Histiocytic and Dendritic Cell Neoplasm": "EFO:1000297", "Wheat streak mosaic virus {http": "NCBITaxon:31741", "GM17761 {http": "CLO:0016601", "asymptomatic myeloma": "EFO:0003073", "CS57615": "EFO:0000033", "Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion": "Orphanet:231130", "Hypoplasia of the corpus callosum {http": "HP:0002079", "Orofaciodigital syndrome type 8": "Orphanet:2755", "riddelliine": "CHEBI:63924", "ILSXISS49/TejJ": "EFO:0002985", "skeletal system disease": "EFO:0002461", "Streptococcus dysgalactiae subsp. dysgalactiae": "NCBITaxon:99822", "infantile epileptic encephalopathy": "EFO:1000643", "Joint hypermobility {http": "HP:0001382", "lufenuron": "CHEBI:39384", "Leber congenital amaurosis": "Orphanet:65", "glycine {http": "CHEBI:15428", "Chromosome X structural anomaly": "Orphanet:98159", "lymphocyte of B lineage": "CL:0000945", "Congenital pulmonary alveolar proteinosis": "Orphanet:264675", "Autosomal recessive intermediate Charcot-Marie-Tooth disease": "Orphanet:268337", "gene trap": "EFO:0004030", "Isolated plagiocephaly": "Orphanet:35098", "Fibronectin glomerulopathy": "Orphanet:84090", "CL-40": "EFO:0006370", "GM17105 {http": "CLO:0014901", "chitin-based cuticle": "UBERON:0001001", "Familial retinoblastoma": "Orphanet:357027", "Developmental malformations - deafness - dystonia": "Orphanet:79107", "Uterine Corpus Lipoleiomyoma": "EFO:1000614", "Endometrial Stromal Nodule": "EFO:1000241", "Oryza sativa Indica Group": "NCBITaxon:39946", "Congenital cataract microcornea with corneal opacity": "Orphanet:289499", "Mosaic-Seq": "EFO:0008820", "LP.01 one leaf visible stage": "PO:0007094", "Familial amyloid polyneuropathy": "Orphanet:85447", "blood urea nitrogen measurement": "EFO:0004741", "age-related macular degeneration": "EFO:0001365", "hordeolum": "EFO:0007315", "Bordetella pertussis": "NCBITaxon:520", "Trichoderma reesei QM6a": "NCBITaxon:431241", "neutrophilic metamyelocyte": "CL:0000582", "nitrogen atom": "CHEBI:25555", "complicated disease course": "EFO:0006820", "Combined oxidative phosphorylation defect type 2": "Orphanet:254920", "CD8-positive, alpha-beta regulatory T cell": "CL:0000795", "Spondyloepimetaphyseal dysplasia - abnormal dentition": "Orphanet:168451", "BG01": "EFO:0007071", "basal-like carcinoma": "EFO:0000281", "Gamma-aminobutyric acid transaminase deficiency": "Orphanet:2066", "Female infertility due to zona pellucida defect": "Orphanet:404466", "GM17158 {http": "CLO:0013965", "Bifidobacterium longum": "NCBITaxon:216816", "Thalassiosira pseudonana CCMP1335": "NCBITaxon:296543", "mesophyll cell": "EFO:0002439", "HSD10 disease, atypical type": "Orphanet:85295", "Benign Childhood Cerebral Neoplasm": "EFO:1000109", "Pectobacterium carotovorum subsp. carotovorum": "NCBITaxon:555", "Rhizomelic chondrodysplasia punctata type 3": "Orphanet:309803", "Congenital unilateral hypoplasia of depressor anguli oris": "Orphanet:1166", "CAL148": "EFO:0005357", "GM17137 {http": "CLO:0015090", "Homocystinuria due to methylene tetrahydrofolate reductase deficiency": "Orphanet:395", "CD34-positive, CD38-positive common myeloid progenitor OR CD34-positive, CD38-positive common lymphoid progenitor": "CL:0000995", "inch": "EFO:0004387", "1,1-bis(2-aminoethyl)-2-hydroxy-3-oxotriazane": "CHEBI:50154", "Stickler syndrome type 1": "Orphanet:90653", "Familial benign chronic pemphigus": "Orphanet:2841", "Pure or complex hereditary spastic paraplegia": "Orphanet:320335", "Populus tremula x Populus tremuloides": "NCBITaxon:47664", "Partial duplication of the short arm of chromosome 2": "Orphanet:262698", "threonate {http": "CHEBI:15243", "Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss": "Orphanet:1171", "Gerbera hybrid cultivar": "NCBITaxon:18101", "circulating cell free DNA measurement": "EFO:0004739", "Spinocerebellar ataxia type 30": "Orphanet:211017", "Kit-positive megakaryocyte progenitor cell": "CL:0002024", "Abnormal thrombosis": "HP:0001977", "COG7-CDG": "Orphanet:79333", "Aniseikonia": "EFO:1001266", "American": "EFO:0003151", "Haemophilus influenzae": "NCBITaxon:727", "alcoholic liver cirrhosis": "EFO:1000802", "micturition": "GO:0060073", "Familial digital arthropathy-brachydactyly": "Orphanet:85169", "ES-D3": "EFO:0005910", "Peroxisomal acyl-CoA oxidase deficiency": "Orphanet:2971", "California encephalitis virus": "NCBITaxon:35305", "Bemisia tabaci": "NCBITaxon:7038", "IgM plasmablast": "CL:0000983", "eotaxin measurement": "EFO:0008122", "KYSE-150": "EFO:0006627", "GM17234 {http": "CLO:0014340", "cachexia": "HP:0004326", "non-neural ectoderm": "UBERON:0005497", "intervertebral disk": "UBERON:0001066", "cardiovascular disease biomarker measurement": "EFO:0005278", "Populus tremuloides": "NCBITaxon:3693", "Lactobacillus delbrueckii subsp. bulgaricus": "NCBITaxon:1585", "fumarate(2-) {http": "CHEBI:29806", "Mantle cell lymphoma": "EFO:1001469", "Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form": "Orphanet:308638", "Carney triad": "Orphanet:139411", "ceramide": "CHEBI:17761", "individual": "EFO:0000542", "HS-5": "EFO:0005282", "Congenital joint dislocations": "Orphanet:294951", "ferrozine monosodium salt": "CHEBI:63942", "Congenital bilateral absence of vas deferens": "Orphanet:48", "Non-syndromic developmental defect of the eye": "Orphanet:108985", "Weiss grade": "EFO:0007060", "4-acetamidobutanoate {http": "CHEBI:11951", "Mild global developmental delay {http": "HP:0011342", "Lissencephaly with cerebellar hypoplasia type D": "Orphanet:100014", "Acidithiobacillus ferrooxidans": "NCBITaxon:920", "Branchio-otic syndrome": "Orphanet:52429", "Hereditary persistence of fetal hemoglobin - beta-thalassemia": "Orphanet:46532", "presumptive rhombomere 5": "UBERON:0007292", "diencephalon neural crest": "UBERON:0003851", "Benign partial infantile seizures": "Orphanet:166311", "male genital tuberculosis": "EFO:1001030", "drug-induced pemphigus": "EFO:0008607", "Ribo-Seq": "EFO:0008891", "Saccharomyces paradoxus NRRL Y-17217": "NCBITaxon:226125", "Felis catus": "NCBITaxon:9685", "library preparation": "OBI:0000711", "Congenital multicore myopathy with external ophthalmoplegia": "Orphanet:98905", "Krabbe disease": "Orphanet:487", "Anonychia with flexural pigmentation": "Orphanet:69125", "retinopathy of prematurity": "EFO:1001158", "Macrodactyly of toes, unilateral": "Orphanet:295243", "Primary basilar impression": "Orphanet:2285", "Charlie M syndrome": "Orphanet:1406", "Infantile neuronal ceroid lipofuscinosis": "Orphanet:79263", "blue nevus": "EFO:1000841", "Streptomyces fradiae": "NCBITaxon:1906", "Glycogen storage disease due to muscle phosphofructokinase deficiency": "Orphanet:371", "GM17278 {http": "CLO:0013204", "GM17214 {http": "CLO:0013886", "apoplast": "GO:0048046", "Drop-Seq": "EFO:0008722", "silo filler's disease": "EFO:1001182", "Partial duplication of the short arm of chromosome 3": "Orphanet:262707", "LAMB2-related infantile-onset nephrotic syndrome": "Orphanet:306507", "NCI-H716": "EFO:0002301", "5-aza-2'-deoxycytidine": "CHEBI:50131", "Listeria monocytogenes": "NCBITaxon:1639", "mature CD8_alpha-low Langerhans cell": "CL:0001020", "Frontonasal dysplasia with alopecia and genital anomaly": "Orphanet:228390", "Triphalangeal thumb - polysyndactyly syndrome": "Orphanet:2950", "Carney complex-trismus-pseudocamptodactyly syndrome": "Orphanet:319340", "frozen specimen": "OBI:0000922", "irritant dermatitis": "EFO:1000718", "material property": "BFO:0000020", "Matthiola incana": "NCBITaxon:3724", "Platyhelminthes life stage": "EFO:0007711", "urothelium": "UBERON:0000365", "GM14581 {http": "CLO:0031585", "1-[1-(1-benzothiophen-2-yl)cyclohexyl]piperidine maleate": "CHEBI:64144", "choroid cancer": "EFO:1000866", "iron ion homeostasis": "EFO:0005882", "Bleeding diathesis due to integrin alpha2-beta1 deficiency": "Orphanet:98886", "thoracic aortic fatty streak": "EFO:0005617", "abiotic plant treatment": "EO:0007191", "Adactyly of foot, unilateral": "Orphanet:295116", "alkylating agent role": "CHEBI:22333", "Chronic mucocutaneous candidosis": "Orphanet:1334", "Phosphoenolpyruvate carboxykinase deficiency": "Orphanet:2880", "pit and fissure surface dental caries": "EFO:0006338", "vasoactive peptide measurement": "EFO:0005196", "SW982": "EFO:0002378", "CA1 field of hippocampus {http": "UBERON:0003881", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A": "Orphanet:308386", "Cocksfoot streak virus": "NCBITaxon:192452", "hypersensitivity vasculitis": "EFO:1000974", "CAL51": "EFO:0005358", "excretion": "GO:0007588", "pneumoconiosis": "Orphanet:182098", "left atrial function": "EFO:0004294", "acute quadriplegic myopathy": "EFO:0000225", "anthrax infection": "EFO:0000778", "thyroid function": "EFO:0004296", "urinary nitrogen measurement": "EFO:0005190", "Glycogen storage disease due to glucose-6-phosphatase deficiency type b": "Orphanet:79259", "pemphigoid gestationis": "EFO:1000709", "protein S measurement": "EFO:0004637", "HuP-T3": "EFO:0006596", "NCI-H520": "EFO:0003124", "preopercle": "UBERON:2000264", "viral RNA data": "EFO:0004605", "carbohydrate metabolic disorder": "EFO:1000061", "dimensionless unit": "UO:0000186", "Mowat-Wilson syndrome due to a ZEB2 point mutation": "Orphanet:261552", "Nectria rigidiuscula": "NCBITaxon:57161", "7q11.23 microduplication syndrome": "Orphanet:96121", "serous adenocarcinoma": "EFO:0003825", "adipose tissue measurement": "EFO:0004764", "Peptic ulcer": "HP:0004398", "ethene": "CHEBI:18153", "UV-sensitive syndrome": "Orphanet:178338", "Non-rhizomelic chondrodysplasia punctata": "Orphanet:176", "Neonatal sepsis": "HP:0040187", "label": "IAO:0000009", "Bunyaviridae infectious disease": "EFO:0007188", "Torticollis - keloids - cryptorchidism - renal dysplasia": "Orphanet:3341", "tryptase beta-2 measurement": "EFO:0008306", "kynurenate {http": "CHEBI:58454", "liver dysplastic nodule": "EFO:0007834", "Cutis laxa-Marfanoid syndrome": "Orphanet:171719", "anatomical system": "UBERON:0000467", "ethyl nitrosourea": "CHEBI:23995", "Chromosomal anomaly": "Orphanet:68335", "NCI-H1882": "EFO:0006665", "Beta-thalassemia with other manifestations": "Orphanet:231386", "hormone": "CHEBI:24621", "Mucopolysaccharidosis type 7": "Orphanet:584", "Lens shape anomaly": "Orphanet:98655", "CAGEscan": "EFO:0008669", "mature Vgamma1.1-positive, Vdelta6.3-positive thymocyte": "CL:0002416", "eye color": "EFO:0003949", "Salvelinus alpinus": "NCBITaxon:8036", "vancomycin trough measurement": "EFO:0007648", "No-0": "EFO:0006976", "antidepressant-induced side effect": "EFO:0006320", "beta-Ala-His dipeptidase measurement": "EFO:0008033", "Peeling skin syndrome type B": "Orphanet:263553", "OUMS-23": "EFO:0006717", "endosperm {http": "PO:0009089", "Aortic Coarctation": "EFO:1001267", "plasma kallikrein measurement": "EFO:0008260", "renal tuberculosis": "EFO:0007463", "SKMEL1": "EFO:0002332", "CaR-1": "EFO:0006548", "Waardenburg syndrome type 1": "Orphanet:894", "Erythropoietic protoporphyria": "Orphanet:79278", "vaccenate(1-) {http": "CHEBI:50498", "SNU-638": "EFO:0006758", "14q12 microdeletion syndrome": "Orphanet:261144", "COLO 792": "EFO:0006377", "HUES62": "EFO:0007087", "purine ribonucleoside biosynthetic process": "GO:0046129", "precursor T-cell lymphoblastic leukemia-lymphoma": "EFO:1001830", "Kasumi-1": "EFO:0006607", "EEG abnormality {http": "HP:0002353", "Hordeum vulgare subsp. spontaneum": "NCBITaxon:77009", "cardiac atrium": "UBERON:0002081", "pulsed doppler echocardiography": "EFO:0003962", "anemia": "EFO:0004272", "Theiler stage 4": "EFO:0004396", "AGS": "EFO:0002109", "presumptive endoderm": "UBERON:0006595", "benzothiadiazole": "CHEBI:48864", "epidemic pleurodynia": "EFO:0007259", "Submandibular Gland Adenocarcinoma": "EFO:1000554", "response to anti-tuberculosis drug": "EFO:0007918", "endothelial cell": "CL:0000115", "mental retardation": "EFO:0003847", "Gastric Choriocarcinoma": "EFO:1000269", "Abnormality of the head": "HP:0000234", "FLOTCH syndrome": "Orphanet:2045", "Sex chromosome disorder of sex development": "Orphanet:325546", "Congenital absence of thigh and lower leg with foot present, bilateral": "Orphanet:295091", "GM12751": "EFO:0001150", "SEM": "EFO:0002326", "Oculocutaneous albinism type 6": "Orphanet:370097", "neurohemal organ": "UBERON:0001053", "scleroderma": "EFO:1001993", "Gibberella moniliformis": "NCBITaxon:117187", "Herpes simplex virus gingivostomatitis": "EFO:0007307", "Rhizomelic chondrodysplasia punctata type 1": "Orphanet:309789", "CEW1": "EFO:0004071", "Arenavirus hemorrhagic fever": "EFO:0007151", "Amelia of lower limb, bilateral": "Orphanet:295059", "Ductal Breast Carcinoma In Situ and Lobular Carcinoma In Situ": "EFO:1000221", "DBA/2J": "EFO:0005184", "hyper-inflammatory immune response": "EFO:0007926", "functional microbiome measurement": "EFO:0007884", "acute promyelocytic leukemia": "EFO:0000224", "lapatinib": "CHEBI:49603", "cartilage element of chondrocranium": "UBERON:0003932", "Sarcoidosis": "Orphanet:797", "compound based treatment": "EFO:0000369", "undifferentiated sarcoma": "EFO:0000730", "population measurement": "EFO:0004557", "Short stature - craniofacial anomalies - genital hypoplasia": "Orphanet:2994", "breast": "UBERON:0000310", "Ectodermal dysplasia - intellectual disability - central nervous system malformation": "Orphanet:1812", "Atypical hypotonia - cystinuria syndrome": "Orphanet:238523", "hand, foot and mouth disease": "EFO:0007294", "Mucinous Gastric Adenocarcinoma": "EFO:1000386", "CS57801": "EFO:0000121", "naphthalene-1,5-diamine": "CHEBI:53003", "Infantile bilateral striatal necrosis": "Orphanet:1576", "Osteogenesis imperfecta type 3": "Orphanet:216812", "P2Y12 defect": "Orphanet:36355", "OE19": "EFO:0002308", "mandible": "UBERON:0001684", "prostate cancer staging": "EFO:0005615", "Distal trisomy 13q": "Orphanet:96105", "LP.02 two leaves visible stage": "PO:0007098", "ectoderm": "UBERON:0000924", "NALM6": "EFO:0002245", "body ratio measurement": "EFO:0007861", "Waardenburg syndrome": "Orphanet:3440", "Cardiac anomalies-developmental delay-facial dysmorphism syndrome": "Orphanet:369891", "tomatidine": "CHEBI:9629", "organochlorine pesticide measurement": "EFO:0007960", "BNAR syndrome": "Orphanet:217266", "Spinal Cord Astrocytoma": "EFO:1000544", "Brachydactyly of toes": "Orphanet:294998", "calcium channel blocker": "CHEBI:38215", "Salivary Gland Pleomorphic Adenoma": "EFO:1000518", "4-hydroxyphenylacetate {http": "CHEBI:48999", "FUM1": "EFO:0000175", "Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency": "Orphanet:276603", "attention function measurement": "EFO:0007636", "blood plasma": "UBERON:0001969", "subacute thyroiditis": "EFO:1001194", "insulin sensitivity measurement": "EFO:0004471", "GM17112 {http": "CLO:0014948", "LP.03 three leaves visible stage": "PO:0007106", "Hereditary hypophosphatemic rickets with hypercalciuria": "Orphanet:157215", "teasterone": "CHEBI:26863", "Atypical Lipomatous Tumor": "EFO:1000099", "DMS79": "EFO:0002166", "spotted colony reporter": "EFO:0005075", "Split hand or/and split foot malformation": "Orphanet:294935", "sebacate(2-) {http": "CHEBI:76283", "differentiated thyroid carcinoma": "EFO:1002017", "HT-SELEX": "EFO:0008769", "Autosomal recessive spastic paraplegia type 55": "Orphanet:320375", "birth rate": "EFO:0004804", "Classic organic aciduria": "Orphanet:79163", "blastula high": "EFO:0001280", "renal medulla": "UBERON:0000362", "CD34-positive, CD38-positive common lymphoid progenitor": "CL:0001021", "GM17239 {http": "CLO:0014327", "Cooks syndrome": "Orphanet:1487", "Oculoauriculovertebral spectrum with radial defects": "Orphanet:2549", "chronic ulcer of skin": "EFO:0007066", "GRO-CAP": "EFO:0008756", "NCI-H2373": "EFO:0006679", "Cardiac Rhabdomyoma": "EFO:1000150", "Fibrous Meningioma": "EFO:1000258", "Distal myopathy with early respiratory muscle involvement": "Orphanet:34521", "migraine without aura": "EFO:0005296", "erucate {http": "CHEBI:32393", "SHAPE-Seq": "EFO:0008922", "Hemihypertrophy": "Orphanet:2128", "HCC1162": "EFO:0006423", "depudecin": "CHEBI:64143", "Familial lipoprotein lipase deficiency": "Orphanet:309015", "longitude": "OBI:0001621", "pharyngeal muscle cell": "EFO:0005497", "ocular tuberculosis": "EFO:1001070", "spinal cord neoplasm": "EFO:0003828", "osteoarthritis, hip": "EFO:1000786", "Arthrogryposis syndrome": "Orphanet:109007", "Tonsillar Squamous Cell Carcinoma": "EFO:1000597", "Disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis": "Orphanet:309463", "GM17804 {http": "CLO:0016497", "GM17245 {http": "CLO:0014415", "Cushing syndrome due to macronodular adrenal hyperplasia": "EFO:0009041", "Ehlers-Danlos syndrome due to tenascin-X deficiency": "Orphanet:230839", "response to bevacizumab": "EFO:0005943", "endothelial growth factor measurement": "EFO:0006900", "GM17741 {http": "CLO:0017020", "renovascular hypertension": "EFO:1001153", "GM17837 {http": "CLO:0016525", "Gonadal dysgenesis, XY type - associated anomalies": "Orphanet:1770", "sample collection protocol": "EFO:0005518", "SITE-Seq": "EFO:0008926", "primary root differentiation zone {http": "PO:0003015", "Yunis-Varon syndrome": "Orphanet:3472", "Lipid storage disease": "Orphanet:79204", "Classic pantothenate kinase-associated neurodegeneration": "Orphanet:216866", "Septo-optic dysplasia": "Orphanet:3157", "mucinous cystadenoma": "EFO:1001048", "Chlamydia pneumoniae seropositivity": "EFO:0007035", "Spondylo-megaepiphyseal-metaphyseal dysplasia": "Orphanet:228387", "Streptococcus equi": "NCBITaxon:1336", "Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation": "Orphanet:289266", "post-traumatic stress disorder symptom measurement": "EFO:0008535", "Diaphragmatic defect - limb deficiency - skull defect": "Orphanet:2141", "steatosis": "EFO:0008527", "Endometrial Undifferentiated Carcinoma": "EFO:1000242", "Encephalitis, Varicella Zoster": "EFO:1001310", "palsy": "EFO:1000631", "spectrophotometer": "OBI:0400115", "CrY2H-seq": "EFO:0008702", "GM17740 {http": "CLO:0017021", "Craniopharyngioma": "EFO:1000209", "Blindness-scoliosis-arachnodactyly syndrome": "Orphanet:171844", "Isolated nail anomaly": "Orphanet:79369", "Glucose transport disorder": "Orphanet:79178", "Dendroctonus ponderosae": "NCBITaxon:77166", "Chlamydomonas reinhardtii": "NCBITaxon:3055", "trypsin-2 measurement": "EFO:0008305", "serum IgG measurement": "EFO:0004565", "Autism - facial port-wine stain": "Orphanet:137911", "abnormality of carbohydrate metabolism/homeostasis": "HP:0011013", "lobular breast carcinoma": "EFO:0008509", "R18": "EFO:0001226", "CS57616": "EFO:0000034", "Streptococcus suis": "NCBITaxon:1307", "omentum": "UBERON:0003688", "malignant hypertension": "EFO:1001031", "stamen abscission zone": "EFO:0002473", "Met-Ala {http": "CHEBI:73610", "Microphthalmia - ankyloblepharon - intellectual disability": "Orphanet:85275", "response to tricyclic antidepressant": "EFO:0007916", "HUES66": "EFO:0007092", "cell adhesion molecule-related/down-regulated by oncogenes measurement": "EFO:0008079", "all-trans-retinoic acid": "CHEBI:15367", "hereditary papulotranslucent acrokeratoderma": "EFO:1000708", "Clostridium tetani": "NCBITaxon:1513", "quinolinate(1-) {http": "CHEBI:46828", "PE/CA-PJ15": "EFO:0006733", "prostate carcinoma": "EFO:0001663", "NCI-H157": "EFO:0003118", "GM12145": "EFO:0001137", "ischemic cardiomyopathy": "EFO:0001425", "NCI-H2287": "EFO:0003122", "Pes cavus {http": "HP:0001761", "Malignant tumor of palpebral epidermis": "Orphanet:98584", "polycystic ovary syndrome": "EFO:0000660", "susceptibility to hepatitis B infection measurement": "EFO:0008405", "Non-syndromic genetic deafness": "Orphanet:87884", "Congenital adrenal hyperplasia": "Orphanet:418", "ES-E14": "EFO:0007075", "choline {http": "CHEBI:15354", "dye role": "CHEBI:37960", "Spartina x townsendii": "NCBITaxon:198504", "renal fibrosis": "EFO:1001517", "Familial scaphocephaly syndrome": "Orphanet:169163", "HPV seropositivity": "EFO:0004510", "CGTHW1": "EFO:0002131", "acidosis": "EFO:1000014", "CS57905": "EFO:0000163", "SW1573": "EFO:0002363", "alveolus": "UBERON:0003215", "systolic heart failure": "EFO:1001207", "4-(trimethylammonio)butanoic acid {http": "CHEBI:1941", "4,4',4''-(4-propylpyrazole-1,3,5-triyl)trisphenol": "CHEBI:64110", "fin": "UBERON:0008897", "Short stature-heart defect-craniofacial anomalies syndrome": "Orphanet:1088", "CD4-positive, CD8-intermediate double-positive thymocyte": "CL:0002431", "deoxycholate {http": "CHEBI:23614", "animal component": "EFO:0000787", "MGC-803": "EFO:0006286", "blood protein measurement": "EFO:0007937", "Isolated focal cortical dysplasia type Ib": "Orphanet:268980", "Strabismus {http": "HP:0000486", "Female restricted epilepsy with intellectual disability": "Orphanet:101039", "ovarian granulosa tumour": "EFO:0006461", "alpha-linolenate {http": "CHEBI:32387", "GM17812 {http": "CLO:0016500", "Hyperlipoproteinemia type 4": "Orphanet:413", "MQ887": "EFO:0004090", "phytosterol measurement": "EFO:0004862", "Syndromic microphthalmia type 5": "Orphanet:178364", "species design": "EFO:0001753", "Neuromuscular disease with dilated cardiomyopathy": "Orphanet:217610", "Epidermolysis bullosa simplex": "Orphanet:304", "mature B cell": "CL:0000785", "Adenoid Cystic Breast Carcinoma": "EFO:1000071", "adipose tissue derived mesenchymal stem cell": "EFO:0005023", "pulmonary tuberculosis": "EFO:1000049", "substrate": "EFO:0005061", "GM14536 {http": "CLO:0031601", "nonadecanoate {http": "CHEBI:78796", "erectile dysfunction": "EFO:0004234", "Conotruncal heart malformations": "Orphanet:2445", "cDNA": "EFO:0008481", "human papilloma virus infection": "EFO:0001668", "NIH3T3-L1": "EFO:0001223", "GM17147 {http": "CLO:0013941", "transposable element identification design": "EFO:0005692", "vitamin E metabolic process": "GO:0042360", "Botrytis cinerea BcDW1 {http": "NCBITaxon:1290391", "Ataxia - hypogonadism - choroidal dystrophy": "Orphanet:1180", "Absence of fingerprints - congenital milia": "Orphanet:1658", "Hyperlipoproteinemia type 3": "Orphanet:412", "Benign Renal Pelvis Neoplasm": "EFO:1000118", "Chemotherapy-induced nausea and vomiting": "EFO:0006911", "Choristoneura fumiferana": "NCBITaxon:7141", "bronchoalveolar adenocarcinoma": "EFO:0000308", "Intractable diarrhea - choanal atresia - eye anomalies": "Orphanet:137622", "mouse embryonic fibroblast cell": "EFO:0004040", "histidine-rich glycoprotein measurement": "EFO:0008155", "Qualitative or quantitative defects of myofibrillar proteins": "Orphanet:209038", "Genetic tumor of hematopoietic and lymphoid tissues": "Orphanet:322126", "Periodic paralysis with transient compartment-like syndrome": "Orphanet:397755", "embryonic antennal sense organ": "FBbt:00005568", "transient ischemic attack": "EFO:0003764", "Osteomesopyknosis": "Orphanet:2777", "serotonergic antagonist": "CHEBI:48279", "microtubule cytoskeleton organization": "GO:0000226", "Central nervous system calcification - deafness - tubular acidosis - anemia": "Orphanet:3240", "Birt-Hogg-Dube Syndrome": "EFO:1001273", "Zebra body myopathy": "Orphanet:97240", "adipose tissue": "UBERON:0001013", "semaphorin-3E measurement": "EFO:0008279", "single-organism transport": "GO:0044765", "AG05416 {http": "CLO:0035232", "Combined oxidative phosphorylation defect type 11": "Orphanet:324535", "gonorrhea": "DOID:7551", "fasudil hydrochloride": "CHEBI:31593", "Propionibacterium freudenreichii subsp. shermanii": "NCBITaxon:1752", "Listeria monocytogenes FSL J2-071": "NCBITaxon:393121", "self vs self design": "EFO:0001777", "polycythemia due to hypoxia": "EFO:0005805", "Malignant Jugulotympanic Paraganglioma": "EFO:1000353", "longitudinal BMI measurement": "EFO:0005937", "plasmacytoid dendritic cell": "CL:0000784", "O-hexanoylcarnitine {http": "CHEBI:70749", "inosine {http": "CHEBI:17596", "osmotic stress treatment": "EO:0001038", "ventral part of telencephalon {http": "UBERON:0000204", "Adult neuronal ceroid lipofuscinosis": "Orphanet:79262", "microRNA profiling by array": "EFO:0000753", "Enterobacteriaceae Infections": "EFO:1001313", "macrophage cell line": "BTO:0002278", "Marvinbryantia formatexigens DSM 14469": "NCBITaxon:478749", "Tomato spotted wilt virus": "NCBITaxon:11613", "reproductive system neoplasm": "EFO:1000051", "Bl-0": "EFO:0005172", "disulfiram": "CHEBI:4659", "Glycogen storage disease due to lactate dehydrogenase deficiency": "Orphanet:2364", "medulla of thymus": "UBERON:0002124", "DN1 thymic pro-T cell": "CL:0000894", "Preaxial polydactyly of fingers": "Orphanet:294939", "Xanthinuria type I": "Orphanet:93601", "Mycoplasma pneumoniae pneumonia": "EFO:0007387", "ventral striatum": "UBERON:0005403", "TR403": "EFO:0004061", "intracranial hypertension": "EFO:1000992", "malathion": "CHEBI:6651", "PEHO-like syndrome": "Orphanet:99807", "Partial trisomy of the short arm of chromosome 9": "Orphanet:262767", "Theiler stage 23": "EFO:0004411", "Holothuria glaberrima": "NCBITaxon:31192", "Haemonchus contortus": "NCBITaxon:6289", "nervous system measurement": "EFO:0005052", "Swiss9": "EFO:0006303", "divanadium pentaoxide": "CHEBI:30045", "primordium": "UBERON:0001048", "all pairs": "EFO:0001763", "SIRPa-positive adipose dendritic cell": "CL:0002463", "pterosphenoid": "UBERON:2000419", "BMI-adjusted fasting blood glucose measurement": "EFO:0008036", "Oculocutaneous albinism type 2": "Orphanet:79432", "Birt-Hogg-Dub\u00c3\u00a9 syndrome": "Orphanet:122", "factor VIII measurement": "EFO:0004630", "kynurenine measurement": "EFO:0008529", "Bacillus subtilis": "NCBITaxon:1423", "Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes": "Orphanet:309136", "GM14478 {http": "CLO:0031529", "L-cysteine glutathione disulfide {http": "CHEBI:21264", "anterior lateral line primordium": "UBERON:2005117", "response to methotrexate": "GO:0031427", "skin wound": "EFO:0005756", "subopercle": "UBERON:2000284", "Craniofrontonasal dysplasia - Poland anomaly": "Orphanet:1521", "Hereditary epidermolysis bullosa associated with ocular features": "Orphanet:263676", "Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency": "Orphanet:93583", "lateral ethmoid": "ZFA:0000226", "SSB-Seq": "EFO:0008949", "Microcephaly - seizures - developmental delay": "Orphanet:228418", "Basement membrane disease": "Orphanet:93550", "Drosophila embryonic structure": "EFO:0003335", "454 GS Junior sequencer": "EFO:0004434", "Pilotto syndrome": "Orphanet:2894", "pyroglutamine measurement": "EFO:0005408", "Craniometaphyseal dysplasia": "Orphanet:1522", "GM06944 {http": "CLO:0036460", "asphyxia neonatorum": "EFO:1000824", "dorsal imaginal precursor": "UBERON:6005831", "Microlissencephaly - micromelia": "Orphanet:50810", "Brachydactyly type A5": "Orphanet:93389", "Fusarium solani": "NCBITaxon:169388", "Familial porphyria cutanea tarda": "EFO:0009043", "Plasmodium berghei": "NCBITaxon:5821", "SALK_049497": "EFO:0001326", "Autosomal recessive amelia": "Orphanet:1027", "CS57842": "EFO:0000141", "Split foot, unilateral": "Orphanet:295124", "HEK293T": "EFO:0001184", "leg": "UBERON:0000978", "GM12871": "EFO:0005344", "postencephalitic Parkinson disease": "EFO:1001402", "growth hormone treatment {http": "EO:0007165", "primitive internal carotid artery": "UBERON:2001053", "limb": "UBERON:0002101", "GlyA-positive erythrocyte": "CL:0002021", "pancreatic adenocarcinoma": "EFO:1000044", "Congenital sucrase-isomaltase deficiency without starch intolerance": "Orphanet:306462", "CS57537": "EFO:0000007", "Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form": "Orphanet:308621", "Reis-B\u00c3\u00bccklers corneal dystrophy": "Orphanet:98961", "small bowel Crohn's disease": "EFO:0005629", "Schwann cell": "CL:0000218", "MAN1B1-CDG": "Orphanet:397941", "PTEN hamartoma tumor syndrome": "Orphanet:306498", "colonic pseudo-obstruction": "EFO:1000871", "Burkholderia cenocepacia": "NCBITaxon:95486", "Cauda equina syndrome": "EFO:0007196", "gamma-glutamylphenylalanine {http": "CHEBI:82966", "Transgrediens et progrediens palmoplantar keratoderma": "Orphanet:495", "ampere": "UO:0000011", "Term-Seq": "EFO:0008968", "hidrocystoma": "EFO:1000967", "Peritoneal Mesothelioma": "EFO:1000467", "Short stature due to GHSR deficiency": "Orphanet:314811", "17alpha-estradiol": "CHEBI:17160", "Pvu-Seal-seq": "EFO:0008876", "Deafness - lymphedema - leukemia": "Orphanet:3226", "overweight body mass index status": "EFO:0005935", "Spinocerebellar ataxia type 14": "Orphanet:98763", "Pelizaeus-Merzbacher-like disease due to GJC2 mutation": "Orphanet:280282", "Pleural Biphasic Mesothelioma": "EFO:1000483", "Kallmann syndrome": "Orphanet:478", "non-gestational choriocarcinoma": "EFO:1001064", "Severe intellectual disability-progressive spastic diplegia syndrome": "Orphanet:404473", "ecdysone": "CHEBI:16688", "occipital lobe": "UBERON:0002021", "Hirschsprung disease - deafness - polydactyly": "Orphanet:2155", "Chia-PET": "EFO:0008684", "Oncorhynchus kisutch": "NCBITaxon:8019", "ER to Golgi transport vesicle": "GO:0030134", "Bruising susceptibility {http": "HP:0000978", "C57BL": "EFO:0005181", "KMS-28PE": "EFO:0006618", "Genetic transient congenital hypothyroidism": "Orphanet:226316", "mating type a": "EFO:0001275", "Crigler-Najjar syndrome": "Orphanet:205", "Bacillus cereus ATCC 14579": "NCBITaxon:226900", "skin neoplasm": "EFO:0004198", "lipid homeostasis": "EFO:0005880", "Autosomal dominant trichoodontoonychodysplasia-syndactyly": "Orphanet:3357", "Renal Colic": "EFO:1001412", "CROP-Seq": "EFO:0008701", "janus kinase-3 deficiency": "EFO:0005565", "Peromyscus polionotus": "NCBITaxon:42413", "Tetramelic monodactyly": "Orphanet:2564", "carbon monoxide": "CHEBI:17245", "Unilateral focal polymicrogyria": "Orphanet:268947", "cirrhosis of liver": "EFO:0001422", "urogenital papilla": "UBERON:2001118", "CS57777": "EFO:0000114", "RERF-LC-MS": "EFO:0002852", "vasculitis": "EFO:0006803", "Daphnia magna": "NCBITaxon:35525", "Pinus resinosa": "NCBITaxon:54921", "Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature": "Orphanet:98352", "2TS22C": "EFO:0006529", "X-linked diffuse leiomyomatosis - Alport syndrome": "Orphanet:1018", "Autosomal dominant Charcot-Marie-Tooth disease type 2C": "Orphanet:99937", "Autosomal dominant limb-girdle muscular dystrophy type 1G": "Orphanet:55596", "BA671": "EFO:0005490", "Malformative syndrome with dentinogenesis imperfecta": "Orphanet:180766", "Alpha-methylacyl-CoA racemase deficiency": "EFO:1001980", "t-tau": "EFO:0007708", "Hh-0": "EFO:0006965", "Familial isolated arrhythmogenic ventricular dysplasia, left dominant form": "Orphanet:293888", "N-methylquipazine dimaleate": "CHEBI:64162", "Yellow Nail Syndrome": "EFO:1001452", "larval labral segment": "UBERON:6001734", "carvacrol": "CHEBI:3440", "Combined immunodeficiency due to CD3gamma deficiency": "Orphanet:169082", "Dentin dysplasia - sclerotic bones": "Orphanet:99792", "Dystonia 16": "Orphanet:210571", "Malignant Adrenal Gland Pheochromocytoma": "EFO:1000348", "Shprintzen-Goldberg syndrome": "Orphanet:2462", "mononuclear osteoclast": "CL:0000778", "NX lymph node stage": "EFO:0004936", "CTLL-2": "EFO:0002821", "CS57740": "EFO:0000082", "collective leaf structure": "PO:0025022", "Atresia of small intestine": "Orphanet:1201", "plant population": "EFO:0005228", "Primary bone dysplasia with decreased bone density": "Orphanet:93446", "AG11513 {http": "CLO:0022604", "Leukocyte-Adhesion Deficiency Syndrome": "EFO:1001359", "radius fracture": "EFO:0003957", "DNA sequencer": "OBI:0400103", "bicuculline": "CHEBI:3092", "platelet reactivity measurement": "EFO:0004985", "Arginine": "Orphanet:35704", "adrenal medulla": "UBERON:0001236", "fetal blood cell": "EFO:0002534", "iloprost": "CHEBI:63916", "cryptorchidism": "EFO:0004562", "Immunodeficiency due to MASP-2 deficiency": "Orphanet:331187", "Streptococcus pyogenes NZ131": "NCBITaxon:471876", "Polydactyly of an index finger, bilateral": "Orphanet:295154", "SUM1315MO2": "EFO:0001239", "Autosomal dominant Charcot-Marie-Tooth disease type 2": "Orphanet:64746", "HMCB": "EFO:0002195", "Thunnus thynnus": "NCBITaxon:8237", "symphytine oxide": "CHEBI:63917", "olfactory placode": "UBERON:0003050", "Familial congenital mirror movements": "Orphanet:238722", "Mitochondrial myopathy and sideroblastic anemia": "Orphanet:2598", "anticholesteremic drug": "CHEBI:35821", "Congenital ichthyosis - intellectual disability - spastic quadriplegia": "Orphanet:352333", "Rickettsia conorii str. Malish 7": "NCBITaxon:272944", "Fanconi anemia complementation group A": "EFO:0009044", "Myotonic dystrophy": "Orphanet:206647", "antifungal drug": "CHEBI:35718", "Clostridium argentinense": "NCBITaxon:29341", "peripartum cardiomyopathy": "EFO:0002628", "mitomycin C": "CHEBI:27504", "complement C1r subcomponent measurement": "EFO:0008090", "progressive multifocal leukoencephalopathy": "EFO:0007455", "Tibial hemimelia": "Orphanet:93322", "2-methylbutyryl-CoA dehydrogenase deficiency": "Orphanet:79157", "parental genotype effect measurement": "EFO:0005939", "fever of unknown origin": "EFO:0003952", "CS57735": "EFO:0000080", "data analyst": "EFO:0001734", "Unspecified mitochondrial disorder": "Orphanet:254837", "Neurofibromatosis type 6": "Orphanet:2678", "Thymoma Type B1": "EFO:1000584", "cot filtration for moderately repetitive genomic DNA": "EFO:0004172", "Epidermolysis bullosa simplex, Dowling-Meara type": "Orphanet:79396", "O-nitrotoluene": "CHEBI:33098", "Spinal muscular atrophy with respiratory distress type 2": "Orphanet:404521", "Primary dystonia, DYT6 type": "Orphanet:98806", "pseudotumor cerebri": "EFO:1001132", "X chromosome number anomaly": "Orphanet:263714", "Plasmodium falciparum": "NCBITaxon:5833", "nitric oxide exhalation measurement": "EFO:0005536", "Distal monosomy 6p": "Orphanet:96125", "GM17178 {http": "CLO:0014029", "Coffin-Siris syndrome": "Orphanet:1465", "short lived plasma cell": "CL:0000975", "Premature aging": "Orphanet:79389", "skin aging measurement": "EFO:0008006", "Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3": "Orphanet:168566", "EFM19": "EFO:0002175", "Rienhoff syndrome": "EFO:1000012", "Syndrome with a symptomatic strabismus": "Orphanet:98683", "TIF-Seq": "EFO:0008970", "serum ST2 measurement": "EFO:0005416", "Focal epilepsy - intellectual disability - cerebro-cerebellar malformation": "Orphanet:352587", "telomere length": "EFO:0004505", "Ile-Gly {http": "CHEBI:74066", "Acromesomelic dysplasia": "Orphanet:93437", "Prader-Willi syndrome": "Orphanet:739", "U373": "EFO:0001255", "Orofaciodigital syndrome type 12": "Orphanet:141327", "fin bud": "UBERON:0002531", "Congenital enteropathy due to enteropeptidase deficiency": "Orphanet:168601", "metatranscriptomic data": "EFO:0004603", "gestational weight gain measurement": "EFO:0008435", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency": "Orphanet:99732", "Fetal Gaucher disease": "Orphanet:85212", "venom gland": "UBERON:0011579", "basophilic promyelocyte": "CL:0000830", "IgM short lived plasma cell": "CL:0000978", "anxiety disorder measurement": "EFO:0007795", "CK syndrome": "Orphanet:251383", "gamma-glutamylthreonine {http": "CHEBI:82968", "Col-1": "EFO:0005149", "Chondrodysplasia punctata, tibial-metacarpal type": "Orphanet:79346", "Cochliobolus sativus": "NCBITaxon:45130", "Oryza sativa Japonica Group": "NCBITaxon:39947", "Magnaporthe oryzae": "NCBITaxon:318829", "A7": "EFO:0002107", "cefazolin": "CHEBI:474053", "neurodevelopmental measurement": "EFO:0008245", "CS57701": "EFO:0000064", "Pure or complex autosomal dominant spastic paraplegia": "Orphanet:320342", "Trichophyton rubrum": "NCBITaxon:5551", "GM17131 {http": "CLO:0015087", "Non-syndromic pontocerebellar hypoplasia": "Orphanet:98523", "Mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA": "Orphanet:254793", "drug-induced akathisia": "EFO:1000903", "Congenital primary lymphedema": "Orphanet:2416", "Bacteroides vulgatus": "NCBITaxon:821", "Qualitative or quantitative defects of protein O-mannose beta1,2N-acetylglucosaminyltransferase": "Orphanet:209024", "tuber {http": "PO:0025522", "cervical incompetence": "EFO:0007202", "erysipelas": "EFO:1001462", "Distal arthrogryposis type 5D": "Orphanet:329457", "Marshall syndrome": "Orphanet:560", "\u00c3\u0085land Islands eye disease": "Orphanet:178333", "Primary glaucoma": "Orphanet:156005", "Ectrodactyly - polydactyly": "Orphanet:1892", "KNS-62": "EFO:0006620", "anti-p200 pemphigoid": "EFO:0008597", "agar stab specimen": "OBI:0000981", "Pitt-Hopkins-like syndrome": "Orphanet:221150", "Illumina NextSeq": "EFO:0008566", "bromobenzene": "CHEBI:3179", "Craniometadiaphyseal dysplasia, wormian bone type": "Orphanet:85184", "developmental disability": "EFO:0003852", "Rare bone disease related to a common gene or pathway defect": "Orphanet:364803", "infectious arthritis": "EFO:1001351", "insulin measurement": "EFO:0004467", "Dihydropyrimidine dehydrogenase deficiency": "Orphanet:1675", "Rare genetic parkinsonian disorder": "Orphanet:307052", "Familial esophageal achalasia": "Orphanet:99723", "organelle envelope lumen": "GO:0031970", "\u00ce\u00a8-seq": "EFO:0008988", "type II NK T cell": "CL:0000922", "Rare hyperthyroidism": "Orphanet:181399", "miliaria": "EFO:1000734", "lupus vulgaris": "EFO:1001023", "openness measurement": "EFO:0007914", "ovarian serous adenocarcinoma": "EFO:0002917", "N-(2-furoyl)glycine {http": "CHEBI:82912", "early rosette growth stage": "PO:0007081", "Canavan disease": "Orphanet:141", "B220-positive CD38-positive naive B cell": "CL:0002109", "phytol": "CHEBI:17327", "Smith-Magenis syndrome": "Orphanet:819", "Platelet storage pool disease": "Orphanet:98454", "SALK_037727": "EFO:0001354", "Theiler stage 15": "EFO:0004406", "lymphogranuloma venereum": "EFO:0007353", "susceptibility to measles measurement": "EFO:0008414", "erythematosquamous dermatosis": "EFO:1000695", "EJM": "EFO:0006572", "cleft palate": "HP:0000175", "Daoy": "EFO:0005698", "Hemarthrosis": "EFO:1001344", "Major Salivary Gland Carcinoma ex Pleomorphic Adenoma": "EFO:1000345", "cefalotin": "CHEBI:124991", "3-hydroxy-3-methylglutarate(2-) {http": "CHEBI:17325", "Carcinoma, Lewis Lung": "EFO:1001770", "full length single cell RNA sequencing": "EFO:0008441", "Genetic bone tumor": "Orphanet:183527", "CD24-positive CD38-negative IgG-negative class switched memory B cell": "CL:0002120", "induced mutation": "EFO:0005315", "placenta disease": "EFO:0007441", "lincomycin": "CHEBI:6472", "Central Nervous System Lymphoma": "EFO:1000157", "hip bone size": "EFO:0004844", "renal sinus adipose tissue measurement": "EFO:0004864", "Christianson syndrome": "Orphanet:85278", "cardiotonic drug": "CHEBI:38147", "Mild hyperphenylalaninemia": "Orphanet:79651", "Se-0": "EFO:0005179", "KRT14-related epidermolysis bullosa simplex": "Orphanet:89838", "visceral": "EFO:0004767", "Autosomal dominant hereditary demyelinating motor and sensory neuropathy": "Orphanet:140453", "Canis lupus": "NCBITaxon:9612", "Nitrosomonas europaea ATCC 19718": "NCBITaxon:228410", "GM17210 {http": "CLO:0013891", "Gelatinous drop-like corneal dystrophy": "Orphanet:98957", "Partial deletion of the long arm of chromosome 13": "Orphanet:262101", "triglyceride change measurement": "EFO:0007681", "Hi-SCL": "EFO:0008763", "GM17155 {http": "CLO:0013960", "Craniosynostosis - cataract": "Orphanet:1530", "Idiopathic syringomyelia": "Orphanet:99858", "dorsal raphe nucleus": "UBERON:0002043", "NCI-H2596": "EFO:0006683", "Intermediate anorectal malformation": "Orphanet:171208", "ILSXISS112/TejJ": "EFO:0003007", "3-hydroxyacyl-CoA dehydrogenase deficiency": "Orphanet:309127", "Disorder of O-N-acetylgalactosaminylglycan synthesis": "Orphanet:309458", "vagal placode 1": "UBERON:2001297", "GM17175 {http": "CLO:0014033", "aleutian mink disease": "EFO:0007139", "21q22.13q22.2 microdeletion syndrome": "Orphanet:268261", "Thumb deformity - alopecia - pigmentation anomaly": "Orphanet:2251", "esterified cholesterol measurement": "EFO:0008589", "Cerebro-costo-mandibular syndrome": "Orphanet:1393", "Ch\u00c3\u00a9diak-Higashi syndrome": "Orphanet:167", "Leydig cell hypoplasia due to partial LH resistance": "Orphanet:96266", "Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency": "Orphanet:35120", "Follicular Cyst": "EFO:1001329", "extra-adrenal sympathetic paraganglioma": "EFO:0000489", "bone neoplasm": "EFO:0003820", "Lactobacillus casei str. Zhang": "NCBITaxon:498216", "Congenital microcephaly {http": "HP:0011451", "organization": "OBI:0000245", "pharyngeal pouch 3": "UBERON:0007124", "Alpha granule disease": "Orphanet:98455", "ND00022 {http": "CLO:0030105", "Essential strabismus": "Orphanet:98682", "prothrombin time measurement": "EFO:0008390", "Autosomal recessive limb-girdle muscular dystrophy type 2N": "Orphanet:206559", "Hyperandrogenism due to cortisone reductase deficiency": "Orphanet:168588", "Rare hemorrhagic disorder due to a platelet receptor defect": "Orphanet:275736", "clear cell renal carcinoma": "EFO:0000349", "mature Vgamma1.1-positive, Vdelta6.3-negative thymocyte": "CL:0002413", "Abnormality of calcium homeostasis": "HP:0004363", "Scophthalmus maximus": "NCBITaxon:52904", "isoxaben": "CHEBI:63956", "pool": "EFO:0000663", "CS57551": "EFO:0000013", "mesectoderm": "UBERON:0000927", "Congenital pseudoarthrosis of clavicle": "Orphanet:66630", "Warthin Tumor": "EFO:1000625", "embryonic central brain glia": "FBbt:00005663", "phorbol 13-acetate 12-myristate": "CHEBI:37537", "Salmonella enterica subsp. enterica serovar Oranienburg": "NCBITaxon:28147", "Gephyrocapsa oceanica": "NCBITaxon:38817", "pauciarticular juvenile rheumatoid arthritis": "EFO:0003114", "mean corpuscular hemoglobin": "EFO:0004527", "PEL-5": "EFO:0002075", "Superficial corneal dystrophy": "Orphanet:98625", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F": "Orphanet:352670", "endometrial stromal sarcoma": "EFO:1000919", "Major hypertriglyceridemia": "Orphanet:181425", "G84": "EFO:0006411", "Saccharomyces cerevisiae S288c": "NCBITaxon:559292", "chemically induced mutation": "EFO:0000370", "vital capacity": "EFO:0004312", "global developmental delay {http": "HP:0001263", "3-(4-hydroxyphenyl)lactate {http": "CHEBI:36659", "Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin": "Orphanet:399983", "Alpha-N-acetylgalactosaminidase deficiency type 3": "Orphanet:79281", "Prochlorococcus marinus": "NCBITaxon:1219", "Pleuronichthys verticalis": "NCBITaxon:195635", "left ventricular function": "EFO:0004295", "Hemophilia": "Orphanet:448", "cotinine measurement": "EFO:0007813", "segmentation stage": "EFO:0001315", "Hemihyperplasia-multiple lipomatosis syndrome": "Orphanet:276280", "cumulus-oocyte complex": "EFO:0002433", "Branchio-oculo-facial syndrome": "Orphanet:1297", "cystatin-SN measurement": "EFO:0008106", "cyclazosin hydrochloride": "CHEBI:63935", "Metaphyseal acroscyphodysplasia": "Orphanet:1240", "Benign Ovarian Endometrioid Tumor": "EFO:1000113", "somatic genotype": "EFO:0004972", "Ralstonia eutropha H16": "NCBITaxon:381666", "antimony(0)": "CHEBI:30304", "heroin dependence": "EFO:0004240", "ILSXISS48/TejJ": "EFO:0002984", "Bilateral generalized polymicrogyria": "Orphanet:208447", "Tarsal-carpal coalition syndrome": "Orphanet:1412", "acrodermatitis": "EFO:1000664", "MDAMB361": "EFO:0001211", "Antecubital pterygium syndrome": "Orphanet:2987", "lympoid tissue": "EFO:1000343", "pulmonary neuroendocrine tumor": "EFO:0005220", "onchocerciasis": "EFO:0007402", "Linear atrophoderma of Moulin": "Orphanet:140933", "Qualitative or quantitative defects of desmin": "Orphanet:209041", "Oscheius dolichura": "NCBITaxon:473156", "nephrotic syndrome": "EFO:0004255", "East Texas bleeding disorder": "Orphanet:391320", "Acute myeloid leukemia with CEBPA somatic mutations": "Orphanet:319480", "caudate nucleus measurement": "EFO:0008387", "Hereditary xanthinuria": "Orphanet:3467", "whole organism": "UBERON:0000468", "Cribriform Carcinoma": "EFO:1000210", "acid": "EFO:0004416", "vagal placode 4": "UBERON:2001300", "curator": "EFO:0001733", "cellular biosynthetic process": "GO:0044249", "Disease with punctate palmoplantar keratoderma as a major feature": "Orphanet:308023", "cell": "CL:0000000", "HT115": "EFO:0006442", "Deafness - encephaloneuropathy - obesity - valvulopathy": "Orphanet:254898", "Fasciitis": "HP:0100537", "Defect in V-ATPase": "Orphanet:309778", "personality": "EFO:0003947", "snDrop-seq": "EFO:0008937", "Mus musculus subspecies": "EFO:0003013", "PCR": "OBI:0000415", "phenylbutazone": "CHEBI:48574", "Ductal or Ductular Proliferation": "EFO:1000222", "YCC3": "EFO:0002880", "Zea mays Mo17 inbred line": "EFO:0007590", "CD22-positive, CD38-low small pre-B cell": "CL:0002053", "pericardial cell primordium": "FBbt:00005466", "pancreatic cell": "EFO:0002966", "limb bone": "UBERON:0002428", "293TsiLL": "EFO:0001083", "tumor necrosis factor receptor superfamily member EDAR measurement": "EFO:0008310", "non-functioning pituitary adenoma": "EFO:0008516", "Cushing syndrome": "EFO:0003099", "HOMA-IR": "EFO:0004501", "troglitazone": "CHEBI:9753", "animal disease": "EFO:0005932", "bucladesine": "CHEBI:50095", "breast cancer cell line": "EFO:0002885", "eye inflammation": "EFO:0005752", "alkaline phosphatase measurement": "EFO:0004533", "cation-independent mannose-6-phosphate receptor measurement": "EFO:0008075", "Pancytopenia due to IKZF1 mutations": "Orphanet:317473", "JHH-5": "EFO:0006602", "Streptopelia risoria": "NCBITaxon:328808", "Torovirus infectious disease": "EFO:0007514", "unit of molarity": "UO:0000061", "septic shock": "EFO:0006834", "Barre-Lieou syndrome": "EFO:0007165", "Maternally-inherited mitochondrial dystonia": "Orphanet:254851", "Poland syndrome": "Orphanet:2911", "fertilizer": "CHEBI:33287", "interleukin 18 receptor 1 measurement": "EFO:0008178", "captopril": "CHEBI:3380", "immature B cell": "CL:0000816", "Hyperbilirubinemia {http": "HP:0002904", "SK-ES-1": "EFO:0002858", "Genetic biliary tract disease": "Orphanet:156607", "iPS-27e": "EFO:0007110", "bulb": "EFO:0001048", "Peters plus syndrome": "Orphanet:709", "CS57752": "EFO:0000087", "purine nucleoside monophosphate metabolic process": "GO:0009126", "central nervous system tuberculosis": "EFO:0007199", "psychosocial stress measurement": "EFO:0006783", "CS57583": "EFO:0000022", "Dyssegmental dysplasia - glaucoma": "Orphanet:1804", "W syndrome": "Orphanet:2804", "PFAPA syndrome": "Orphanet:42642", "ethylenediaminetetraacetic acid": "CHEBI:42191", "Qualitative or quantitative defects of titin": "Orphanet:209053", "Prolactin-Producing Pituitary Gland Carcinoma": "EFO:1000497", "intermediate trophoblast cell": "CL:0002217", "Ocular coloboma": "Orphanet:194", "milligram per deciliter": "EFO:0004374", "endocrine system": "UBERON:0000949", "obstructive jaundice": "EFO:1001068", "Zygodactyly type 2": "Orphanet:295189", "Isolated brachycephaly": "Orphanet:35099", "Spondylometaphyseal dysplasia, A4 type": "Orphanet:168555", "Mucolipidosis type 2": "Orphanet:576", "RNA-seq of non coding RNA": "EFO:0003737", "Nephropathy secondary to a storage or other metabolic disease": "Orphanet:93593", "rhombomere 6": "UBERON:0005519", "EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood": "EFO:1000228", "triiodothyronine measurement": "EFO:0008392", "data coder": "EFO:0001735", "vincristine": "CHEBI:28445", "hymenolepiasis": "EFO:0007317", "colitis": "EFO:0003872", "Pyruvate carboxylase deficiency, infantile form": "Orphanet:353308", "perinatal jaundice due to hepatocellular damage": "EFO:1000750", "Isolated agammaglobulinemia": "Orphanet:229717", "Growth Hormone-Producing Pituitary Gland Adenoma": "EFO:1000287", "Non-immune hydrops fetalis": "EFO:0009051", "Cortical blindness - intellectual disability - polydactyly": "Orphanet:1389", "response to bronchodilator": "GO:0097366", "NCI-H295R": "EFO:0002289", "PSI-seq": "EFO:0008873", "Lytechinus pictus": "NCBITaxon:7653", "Primary progressive aphasia": "EFO:0009053", "pelvis": "UBERON:0002355", "Thymic Small Cell Carcinoma": "EFO:1000578", "Chara corallina": "NCBITaxon:43696", "Fructose-1,6-bisphosphatase deficiency": "Orphanet:348", "Hennekam syndrome": "Orphanet:2136", "GM11995": "EFO:0001127", "CLN7 disease": "Orphanet:228366", "Legionella pneumophila subsp. pneumophila str. Philadelphia 1": "NCBITaxon:272624", "Juberg-Hayward syndrome": "Orphanet:2319", "Oculocutaneous albinism type 4": "Orphanet:79435", "Acropora millepora": "NCBITaxon:45264", "obsessive-compulsive disorder": "EFO:0004242", "centrifuge": "OBI:0400106", "Toriello-Carey syndrome": "Orphanet:3338", "panophthalmitis": "EFO:1001081", "Charcot-Marie-Tooth disease type 1E": "Orphanet:90658", "Epidermodysplasia verruciformis": "Orphanet:302", "Pinta": "EFO:1001396", "gene": "SO:0000704", "IL.00 inflorescence just visible stage": "PO:0007006", "BRIC-seq": "EFO:0008660", "erythrocyte measurement": "EFO:0005047", "Orientia tsutsugamushi": "NCBITaxon:784", "Congenital analbuminemia": "Orphanet:86816", "GM17835 {http": "CLO:0016520", "endocrine system component": "UBERON:6007435", "pseudohermaphroditism": "EFO:0005579", "fascioloidiasis": "EFO:0007268", "gastrula 75%-epiboly": "EFO:0001292", "C-C motif chemokine 15 measurement": "EFO:0008043", "Roberstonian translocation": "EFO:0004023", "pericardial tuberculosis": "EFO:0007426", "Bothnia retinal dystrophy": "Orphanet:85128", "GM17755 {http": "CLO:0016555", "Permanent neonatal diabetes mellitus": "Orphanet:99885", "Oryza rufipogon": "NCBITaxon:4529", "uterine neoplasm": "EFO:0003859", "Chronic Neutrophilic Leukemia": "EFO:1000179", "SOLiD native csfasta format": "EFO:0004159", "corneal epithelial cell": "BTO:0004298", "Hereditary renal hypouricemia": "Orphanet:94088", "Spina bifida cystica": "Orphanet:268744", "aorta endothelium": "UBERON:0004851", "NCI-H1694": "EFO:0002263", "Ichthyosis hystrix gravior": "Orphanet:79504", "thrombin generation potential measurement": "EFO:0005538", "LP.17 seventeen leaves visible stage": "PO:0007067", "Western equine encephalitis": "EFO:0007546", "Congenital blindness due to retinal non-attachment": "Orphanet:300337", "freshwater sediment metagenome": "NCBITaxon:556182", "shigellosis": "EFO:0005585", "Combined oxidative phosphorylation defect type 24": "EFO:0009034", "circular visceral mesoderm primordium": "EFO:0000344", "methyl methanesulfonate": "CHEBI:25255", "secondary Parkinson disease": "EFO:1001175", "blood island": "UBERON:0003061", "carbon": "CHEBI:27594", "quality control testing design": "EFO:0001774", "Trisomy Xq28": "Orphanet:1762", "Hern\u00c3\u00a1ndez-Aguirre Negrete syndrome": "Orphanet:2139", "Rare genetic medullar disease": "Orphanet:183515", "SCN2.2": "EFO:0002708", "CD2-positive, CD5-positive, CD44-positive alpha-beta intraepithelial T cell": "CL:0002037", "multiple symmetric lipomatosis": "EFO:1000737", "Ichthyosis-hypotrichosis syndrome": "Orphanet:91132", "nervous system developmental tissue": "EFO:0001903", "hypercholesterolemia": "HP:0003124", "atopic eczema": "EFO:0000274", "diffuse esophageal spasm": "EFO:1001785", "Clostridium baratii": "NCBITaxon:1561", "Hyperlipidemia due to hepatic triglyceride lipase deficiency": "Orphanet:140905", "otic placode": "UBERON:0003069", "Familial multiple trichoepithelioma": "Orphanet:867", "myristoleate {http": "CHEBI:32370", "Cryptococcus neoformans var. neoformans": "NCBITaxon:40410", "Lissencephaly": "Orphanet:48471", "MRE-seq": "EFO:0003748", "HCS data analysis protocol": "EFO:0007573", "Hemolytic anemia due to adenylate kinase deficiency": "Orphanet:86817", "Juvenile nephronophthisis": "Orphanet:93592", "Child Behaviour Checklist assessment": "EFO:0005661", "TT3E": "EFO:0002868", "Machado-Joseph disease type 3": "Orphanet:276244", "GMS syndrome": "Orphanet:2090", "embryonic epipharynx": "FBbt:00005614", "Juvenile Xanthogranuloma": "EFO:1000311", "leucine carboxyl methyltransferase 1 measurement": "EFO:0008207", "Peyer's patch B cell": "CL:0002402", "self rated health": "EFO:0004778", "Dickeya dadantii": "NCBITaxon:204038", "(+)-alpha-tocopherol": "CHEBI:18145", "GM17263 {http": "CLO:0013169", "alpha-1-antitrypsin measurement": "EFO:0008327", "Obesity due to SIM1 deficiency": "Orphanet:369873", "LP.15 fifteen leaves visible stage": "PO:0007104", "MiR\u00e2\u0080\u0090CLIP": "EFO:0008815", "brain infarction": "EFO:0004277", "lymphocyte": "CL:0000542", "GM17135 {http": "CLO:0015094", "dorsal ectoderm anlage in statu nascendi": "EFO:0000415", "GM17133 {http": "CLO:0015082", "HCC461": "EFO:0003134", "Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes": "Orphanet:93221", "Mild phenylketonuria": "Orphanet:79253", "OCUM-1": "EFO:0006714", "hairy cell leukemia": "EFO:1000956", "Biemond syndrome type 2": "Orphanet:141333", "Autosomal dominant Charcot-Marie-Tooth disease type 2B": "Orphanet:99936", "Mosaic trisomy 2": "Orphanet:1723", "GM12057": "EFO:0001135", "Primary hypertrophic osteoarthropathy": "Orphanet:248095", "American trypanosomiasis": "EFO:0008559", "Ustilago maydis": "NCBITaxon:5270", "3-(5-fluorouracil-1-yl)-L-alanine": "CHEBI:42549", "Heliconius erato petiverana": "NCBITaxon:64531", "PLATE-Seq": "EFO:0008863", "pupa": "UBERON:0003143", "cyclooxygenase 1 inhibitor": "CHEBI:50630", "tick infestation": "EFO:0007508", "susceptibility to strep throat measurement": "EFO:0008408", "Osteosclerosis-developmental delay-craniosynostosis syndrome": "Orphanet:178377", "Benign Adrenal Gland Pheochromocytoma": "EFO:1000106", "Congenital communicating hydrocephalus": "Orphanet:269505", "Pro-Ala {http": "CHEBI:74753", "long non polyA RNA": "EFO:0005018", "Eucalyptus nitens": "NCBITaxon:87674", "vaso-occlusive pain measurement": "EFO:0008316", "Chondroectodermal dysplasia with night blindness": "Orphanet:319195", "response to biological dust exposure": "EFO:0006992", "experimental stage": "EFO:0007554", "aphidicolin": "CHEBI:2766", "pigmentation disease": "EFO:1000755", "CHST3-related skeletal dysplasia": "Orphanet:263463", "knee": "UBERON:0001465", "ATC Code A Alimentary tract and metabolism": "EFO:0005633", "dose": "EFO:0000428", "interleukin-13 (Homo sapiens)": "EFO:0003797", "Autosomal ichthyosis syndrome with fatal disease course": "Orphanet:281241", "Pyruvate dehydrogenase E1-alpha deficiency": "Orphanet:79243", "foetal structure": "EFO:0002462", "height-adjusted body mass index": "EFO:0005851", "hippocampal atrophy": "EFO:0005039", "persistent fetal circulation syndrome": "EFO:1001103", "Hereditary thermosensitive neuropathy": "Orphanet:84093", "electroencephalogram measurement": "EFO:0004357", "Centronuclear myopathy": "Orphanet:595", "AB SOLiD PI System": "EFO:0004437", "diffuse alveolar-septal amyloidosis": "EFO:1001885", "preeclampsia": "EFO:0000668", "Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome": "Orphanet:37042", "CS57709": "EFO:0000068", "SIG-M5": "EFO:0006751", "Bifidobacterium": "NCBITaxon:1678", "Hermansky-Pudlak syndrome type 7": "Orphanet:231531", "epiandrosterone sulfate {http": "CHEBI:83040", "Recessive hereditary methemoglobinemia type 1": "Orphanet:139373", "T follicular helper cell": "CL:0002038", "MEL-GATA-1-ER {http": "EFO:0005480", "regulatory B cell": "CL:0000969", "Adrenocorticotropic hormone deficiency": "EFO:1001979", "Gorilla gorilla gorilla": "NCBITaxon:9595", "Hurler syndrome": "Orphanet:93473", "Pleural Sarcomatoid Mesothelioma": "EFO:1000486", "Autosomal recessive spastic paraplegia type 21": "Orphanet:101001", "PARC syndrome": "Orphanet:2825", "Axonal Charcot-Marie-Tooth disease with acrodystrophy": "Orphanet:90119", "Citrus limon": "NCBITaxon:2708", "Meige disease": "Orphanet:90186", "pseudolymphoma": "EFO:1001831", "46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency": "Orphanet:752", "Cernunnos-XLF deficiency": "Orphanet:169079", "O-butanoylcarnitine {http": "CHEBI:7676", "2q23.1 microduplication syndrome": "Orphanet:313947", "Pseudomonas putida": "NCBITaxon:303", "CD7-negative lymphoid progenitor cell": "CL:0001027", "S1": "EFO:0002078", "Partial trisomy of the long arm of chromosome 20": "Orphanet:262995", "apical ectodermal ridge pelvic fin bud": "ZFA:0001385", "Sphingomonas paucimobilis": "NCBITaxon:13689", "hyperpigmentation of eyelid": "EFO:1000711", "N(alpha)-acetyl-L-arginine {http": "CHEBI:40521", "purine ribonucleotide metabolic process": "GO:0009150", "small nuclear ribonucleoprotein F measurement": "EFO:0008288", "Rothmund-Thomson syndrome type 2": "Orphanet:221016", "mitochondrion localization": "GO:0051646", "IgG short lived plasma cell": "CL:0000977", "Isochromosomy Yp": "Orphanet:98797", "Xanthomonas campestris pv. campestris": "NCBITaxon:340", "hypertensive retinopathy": "EFO:1000977", "UM-UC-1": "EFO:0006770", "X-linked dystonia-parkinsonism": "Orphanet:53351", "Pseudohypoparathyroidism type 2": "Orphanet:94090", "Gaucher disease type 2": "Orphanet:77260", "Peripheral precocious puberty": "Orphanet:178040", "norflurazon": "CHEBI:50842", "Lactobacillus plantarum": "NCBITaxon:1590", "Benign recurrent intrahepatic cholestasis type 2": "Orphanet:99961", "embryonic cuprophilic cell": "EFO:0000450", "Axial spondylometaphyseal dysplasia": "Orphanet:168549", "polyarticular juvenile idiopathic arthritis, rheumatoid factor negative": "EFO:1002020", "Drosophila montana": "NCBITaxon:40370", "Acrocapitofemoral dysplasia": "Orphanet:63446", "Clostridium beijerinckii NCIMB 8052": "NCBITaxon:290402", "11p15.4 microduplication syndrome": "Orphanet:300305", "X-linked retinoschisis": "Orphanet:792", "N-acetylneuraminate {http": "CHEBI:35418", "response to silica exposure": "EFO:0005853", "vascular cord": "UBERON:0006965", "Amapari virus": "NCBITaxon:45218", "Salmonella enterica subsp. enterica serovar Enteritidis": "NCBITaxon:149539", "interleukin-17 (Mus musculus)": "EFO:0003800", "Abnormality of lipid metabolism": "HP:0003119", "GM10248": "EFO:0005334", "Anopheles funestus": "NCBITaxon:62324", "inflorescence {http": "PO:0009049", "Patellar dysostosis": "Orphanet:93455", "gram per kilogram": "EFO:0002897", "GM12154": "EFO:0001139", "Allium cepa": "NCBITaxon:4679", "Sclerosteosis": "Orphanet:3152", "Cucurbita maxima": "NCBITaxon:3661", "myelosuppression": "EFO:0007053", "small cell carcinoma": "EFO:0008524", "Aba-seq": "EFO:0008649", "arteriosclerosis obliterans": "EFO:1000820", "Generalized epidermolysis bullosa simplex, non-Dowling-Meara type": "Orphanet:79399", "Stickler syndrome type 2": "Orphanet:90654", "age at assessment": "EFO:0008007", "Bilateral renal hypoplasia": "Orphanet:97362", "zebularine {http": "CHEBI:46938", "platelet measurement": "EFO:0005036", "Pneumopericardium": "EFO:1001400", "Lissencephaly type 3 - metacarpal bone dysplasia": "Orphanet:86822", "Autosomal recessive intermediate Charcot-Marie-Tooth disease type A": "Orphanet:217055", "Kluver-Bucy syndrome": "EFO:0007335", "rhombomere 7 floor plate": "UBERON:0005585", "Intermittent hydrarthrosis": "Orphanet:329967", "hybridization chamber": "OBI:0400110", "eating behaviour": "EFO:0007829", "sphinganine-1-phosphate {http": "CHEBI:16893", "ML-DmD11": "EFO:0005824", "protein glycosylation": "GO:0006486", "Distal trisomy 7p": "Orphanet:96074", "Dimethylglycine dehydrogenase deficiency": "Orphanet:243343", "Hypophosphatasia": "Orphanet:436", "GM02783 {http": "CLO:0014788", "Astroviridae infectious disease": "EFO:0007158", "Basal encephalocele": "Orphanet:268829", "Mosaic trisomy 16": "Orphanet:1708", "Isolated scaphocephaly": "Orphanet:35093", "SMIT": "EFO:0008934", "complement factor B measurement": "EFO:0008096", "stem Cell Factor measurement": "EFO:0008291", "X-linked intellectual disability, Schimke type": "Orphanet:85285", "Penicillium funiculosum": "NCBITaxon:28572", "Rare syndromic dyslipidemia": "Orphanet:181437", "Neurenteric cyst": "Orphanet:268865", "GlyA-positive reticulocytes": "CL:0002020", "glutathione": "CHEBI:16856", "Acromesomelic dysplasia, Grebe type": "Orphanet:2098", "Neutrophil immunodeficiency syndrome": "Orphanet:183707", "Alopecia universalis": "Orphanet:701", "steatitis": "EFO:1001191", "Immunodeficiency with factor H anomaly": "Orphanet:200421", "ring stage trophozoite": "EFO:0002590", "marine metagenome": "NCBITaxon:408172", "Anemonia viridis": "NCBITaxon:51769", "UCSF4": "EFO:0007116", "acrocephalosyndactylia": "EFO:0004123", "progressive external ophthalmoplegia": "EFO:0002509", "phenol red": "CHEBI:31991", "15q11.2 microdeletion syndrome": "Orphanet:261183", "Abnormality of the skull": "HP:0000929", "nicotinic acid": "CHEBI:15940", "48,XYYY syndrome": "Orphanet:99329", "Congenitally uncorrected transposition of the great arteries": "Orphanet:860", "Salmo salar": "NCBITaxon:8030", "elephantiasis": "EFO:0004711", "CD38-negative IgG-negative class switched memory B cell": "CL:0002118", "X-linked immunoneurologic disorder": "Orphanet:2571", "MRCS syndrome": "Orphanet:263347", "Hemochromatosis type 4": "Orphanet:139491", "Lethal Larsen-like syndrome": "Orphanet:2371", "subvalvular aortic stenosis": "EFO:1001199", "GM17230 {http": "CLO:0014347", "platelet aggregation": "GO:0070527", "proliferative vitreoretinopathy": "EFO:1001129", "non-HDL cholesterol": "EFO:0007931", "congenital heart disease": "EFO:0005207", "alcohol dependence": "EFO:0003829", "matrilysin measurement": "EFO:0008227", "presumptive ectoderm": "UBERON:0006601", "Spastic paraplegia - nephritis - deafness": "Orphanet:2820", "data transformation": "OBI:0200000", "Loucy": "EFO:0007112", "GM17202 {http": "CLO:0013837", "Desulfovibrio vulgaris": "NCBITaxon:881", "statoacoustic (VIII) ganglion": "UBERON:0002827", "response to serotonin-norephinephrine reuptake inhibitor": "EFO:0006325", "iPS-17b": "EFO:0007104", "Isolated anophthalmia - microphthalmia": "Orphanet:2542", "NCI-H2595": "EFO:0006682", "Odontomatosis - aortae esophagus stenosis": "Orphanet:2724", "Borderline Ovarian Brenner Tumor": "EFO:1000135", "kidney cell": "CL:1000497", "ovarian reserve": "EFO:0004770", "warm/hot air temperature regimen {http": "EO:0007319", "Purpura": "HP:0000979", "Tuberculosis, Cardiovascular": "EFO:1001442", "theileriasis": "EFO:0007506", "bortezomib": "CHEBI:52717", "Disorder of energy metabolism": "Orphanet:79200", "4T1": "EFO:0002037", "Metachondromatosis": "Orphanet:2499", "B220-positive CD38-positive IgG-negative class switched memory B cell": "CL:0002122", "trabecular layer": "UBERON:0004124", "Isolated congenital microcephaly": "Orphanet:199642", "Mucolipidosis type 3": "Orphanet:577", "Dystonia {http": "HP:0001332", "tartrate(2-) {http": "CHEBI:15193", "caudal artery": "UBERON:0003086", "xanthurenate {http": "CHEBI:71201", "GM02767 {http": "CLO:0014806", "ochratoxin A": "CHEBI:7719", "sensorineural hearing loss": "EFO:1001176", "keratocyte": "CL:0002363", "Pulverulent cataract": "Orphanet:98984", "array control reporter size": "EFO:0005439", "gametophyte meristematic apical cell {http": "PO:0030014", "SUDHL5": "EFO:0002356", "sodium metaarsenite": "CHEBI:29678", "mild disease course": "EFO:0006819", "Dystrophic epidermolysis bullosa, nails only": "Orphanet:158676", "Oculomaxillofacial dysostosis": "Orphanet:1794", "temporal lobe": "UBERON:0001871", "HPL1D": "EFO:0006909", "Rhabditis remanei": "NCBITaxon:446304", "Safe-SeqS": "EFO:0008901", "glucose homeostasis measurement": "EFO:0006896", "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia": "Orphanet:284324", "Desulfovibrio halophilus": "NCBITaxon:45629", "Amelia of upper limb, unilateral": "Orphanet:295053", "longitudinal alcohol consumption measurement": "EFO:0007645", "Columnar Cell Hyperplasia of the Breast": "EFO:1000199", "lipoma": "EFO:0000759", "hip": "UBERON:0001464", "MS-1": "EFO:0002836", "rapamycin": "CHEBI:9168", "Congenital bowing of long bones": "Orphanet:2292", "Postaxial polydactyly of toes": "Orphanet:295008", "interleukin-20 (Homo sapiens)": "EFO:0003803", "ORGANIC": "EFO:0008838", "X-linked dyserythropoetic anemia with abnormal platelets and neutropenia": "Orphanet:363727", "Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis": "Orphanet:137631", "nucleus accumbens volume": "EFO:0006931", "generational effect measurement": "EFO:0008364", "B cell": "CL:0000236", "Turcot syndrome with polyposis": "Orphanet:99818", "snRNA-seq": "EFO:0008940", "eosinophilic promyelocyte": "CL:0000833", "Pyruvate carboxylase deficiency": "Orphanet:3008", "Autosomal dominant severe congenital neutropenia": "Orphanet:486", "methionine aminopeptidase 2 measurement": "EFO:0008232", "Sinonasal Undifferentiated Carcinoma": "EFO:1000527", "tiredness measurement": "EFO:0007946", "hearing loss": "EFO:0004238", "neonatal jaundice": "EFO:1000739", "response to citalopram": "EFO:0006329", "external control ratio": "EFO:0000488", "COLO 680N": "EFO:0006373", "Wrinkly skin syndrome": "Orphanet:2834", "Pneumocephalus": "EFO:1001398", "Francisella tularensis subsp. tularensis SCHU S4": "NCBITaxon:177416", "X-linked intellectual disability, Cabezas type": "Orphanet:85293", "CD9-positive, CD41-positive megakaryocyte cell": "CL:0002027", "Congenital ptosis": "Orphanet:91411", "age at death": "EFO:0005056", "natural cytotoxicity triggering receptor 3 measurement": "EFO:0008243", "trench fever": "EFO:0007519", "bulbus arteriosus": "UBERON:0004152", "neurodegenerative disease": "EFO:0005772", "rifampicin": "CHEBI:28077", "2,4,6-trinitrotoluene": "CHEBI:46053", "ocular toxoplasmosis": "EFO:0007399", "Postaxial polydactyly of toes, unilateral": "Orphanet:295179", "Bartonella grahamii": "NCBITaxon:33045", "adrenal cortex": "UBERON:0001235", "liver disease biomarker": "EFO:0006845", "anaplastic oligodendroglioma": "EFO:0002501", "Constitutional anemia due to iron metabolism disorder": "Orphanet:98360", "CaSki": "EFO:0006549", "lymphadenitis": "HP:0002840", "paraxial mesoderm": "UBERON:0003077", "response to tetracyclic antidepressant": "EFO:0007917", "EM435": "EFO:0004070", "response to diclofenac": "EFO:0007919", "KP-4": "EFO:0006623", "apolipoprotein E measurement": "EFO:0008029", "rhombomere 8 floor plate": "UBERON:0005588", "Lilium hybrid division VII": "NCBITaxon:101269", "epithelium of small intestine": "UBERON:0001902", "Mixed Tumor, Mesodermal": "EFO:1001371", "carotid artery endothelium": "UBERON:0019189", "Qualitative or quantitative defects of protein SERCA1": "Orphanet:209199", "lateral root cap": "PO:0020131", "erlotinib": "CHEBI:114785", "epilepsia partialis continua": "EFO:1000924", "105KC": "EFO:0006354", "pro-NK cell": "CL:0000825", "Rapid Amplification of cDNA Ends": "EFO:0004182", "seborrheic infantile dermatitis": "EFO:1000765", "Chagas cardiomyopathy": "EFO:0005529", "Morvan syndrome": "EFO:1001897", "disseminated atypical mycobacterial infection": "EFO:1001498", "internal carotid artery stenosis": "EFO:0002615", "Z-138 {http": "EFO:0005479", "CCD-25Lu": "EFO:0005364", "Polyarteritis Nodosa": "EFO:0009012", "response to selective serotonin reuptake inhibitor": "EFO:0005658", "NCI-H929": "EFO:0001221", "washing": "EFO:0000735", "family based design": "EFO:0001429", "Solenopsis invicta": "NCBITaxon:13686", "IgG-negative double negative memory B cell": "CL:0002104", "acute": "HP:0011009", "Prolidase deficiency": "Orphanet:742", "pursuit maintenance gain measurement": "EFO:0008433", "CD56-negative, CD161-positive immature natural killer cell": "CL:0002344", "X-linked non-syndromic sensorineural deafness type DFN": "Orphanet:90625", "sulindac sulfone": "CHEBI:64212", "454 GS 20 standard manufacturer's protocol": "EFO:0005051", "nanomolar": "UO:0000065", "classical monocyte": "CL:0000860", "MitoRCA-seq": "EFO:0008817", "Disease associated with non-acquired combined pituitary hormone deficiency": "Orphanet:95495", "CESS": "EFO:0002130", "mesodermal cell": "CL:0000222", "3-methylhistidine {http": "CHEBI:70959", "Atresia of urethra": "Orphanet:105", "Tricho-dento-osseous syndrome": "Orphanet:3352", "carotid artery internal diameter measurement": "EFO:0007720", "gastrula germ-ring": "EFO:0001295", "metastatic colorectal cancer": "EFO:1001480", "array manufacturer": "EFO:0001728", "microsatellite instability measurement": "EFO:0007054", "Salmonella enterica subsp. enterica serovar Kentucky": "NCBITaxon:192955", "OCI-AML2": "EFO:0006706", "primitive red blood cell": "CL:0002355", "Non-distal monosomy 12q": "Orphanet:96160", "Bm5 B cell": "CL:0000967", "BT474": "EFO:0001093", "Pyomyositis": "EFO:1001409", "biliary system": "UBERON:0002294", "subcutaneous adipose tissue": "UBERON:0002190", "TH-2": "EFO:0002804", "MERFISH": "EFO:0008992", "Caenorhabditis briggsae": "NCBITaxon:6238", "G111": "EFO:0006395", "intracellular non-membrane-bounded organelle": "GO:0043232", "Open iniencephaly": "Orphanet:268363", "tongue squamous cell carcinoma": "EFO:1000055", "Methylcobalamin deficiency type cblDv1": "Orphanet:308380", "MOLP-2": "EFO:0006653", "mitochondrial respiratory-chain inhibitor": "CHEBI:25355", "perception of facial expression": "EFO:0004823", "trichostrongylosis": "EFO:0007523", "Solea senegalensis": "NCBITaxon:28829", "epiglottitis": "EFO:0007261", "Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay": "Orphanet:73246", "uterus fundus": "EFO:0005186", "myelin sheath": "GO:0043209", "CD34-positive, CD38-positive eosinophil progenitor cell": "CL:0002008", "GM17183 {http": "CLO:0013753", "MHC-II-positive classical monocyte": "CL:0002470", "Primary immunodeficiency due to a defect in innate immunity": "Orphanet:101988", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B": "Orphanet:100044", "COLO 206F": "EFO:0006554", "duplication": "EFO:0004015", "interleukin-24 (Homo sapiens)": "EFO:0003805", "Prader-Willi syndrome due to translocation": "Orphanet:177907", "Upper limb defect - eye and ear abnormalities": "Orphanet:2489", "Tumoral calcinosis": "Orphanet:53715", "Multiple congenital anomalies/dysmorphic syndrome-intellectual disability": "Orphanet:102283", "Combined oxidative phosphorylation defect type 27": "EFO:0009037", "Abdominal distention": "HP:0003270", "Swiss3": "EFO:0006300", "optic rim area measurement": "EFO:0006938", "early telencephalic vesicle": "UBERON:0009676", "Genetic periodic paralysis": "Orphanet:371433", "Micropenis {http": "HP:0000054", "alcohol dependence measurement": "EFO:0007835", "thrombin activatable fibrinolysis inhibitor activation peptide measurement": "EFO:0008582", "segmental intercostal artery": "UBERON:2000677", "Monosiga brevicollis": "NCBITaxon:81824", "MDAMB453": "EFO:0001215", "Vitiligo": "EFO:0004208", "amnioserosa anlage in statu nascendi": "FBbt:00005422", "docosahexaenoic acid {http": "CHEBI:36005", "Ankyloblepharon filiforme - imperforate anus": "Orphanet:1074", "Methylmalonic aciduria due to transcobalamin receptor defect": "Orphanet:280183", "Arrhinia - choanal atresia - microphthalmia": "Orphanet:1135", "epigallocatechin gallate": "CHEBI:4806", "Dentinogenesis imperfecta - short stature - hearing loss - intellectual disability": "Orphanet:71267", "manic episode measurement": "EFO:0007705", "AsPC1": "EFO:0002112", "Staphylococcus carnosus": "NCBITaxon:1281", "Bronchopulmonary dysplasia": "Orphanet:70589", "cholecystolithiasis": "EFO:1000864", "Ptosis - strabismus - ectopic pupils": "Orphanet:2999", "Porphyria due to ALA dehydratase deficiency": "Orphanet:100924", "fear of minor pain measurement": "EFO:0008340", "T-helper 1 cell": "CL:0000545", "random RNA-Seq across whole transcriptome": "EFO:0004158", "Adenoviridae Infections": "EFO:1001259", "mesangial phagocyte": "CL:0000777", "asymptomatic neurocognitive impairment": "EFO:0007983", "interleukin-1 beta measurement": "EFO:0004812", "NCI-H1573": "EFO:0002256", "Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies": "Orphanet:2443", "X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency": "Orphanet:319612", "cecal benign neoplasm": "EFO:0007197", "Muscular dystrophy - white matter spongiosis": "Orphanet:1877", "Extrahepatic Bile Duct Squamous Cell Carcinoma": "EFO:1000248", "Nocturnal Paroxysmal Dystonia": "EFO:1001381", "Colletotrichum graminicola {http": "NCBITaxon:31870", "O-isovalerylcarnitine {http": "CHEBI:73025", "BALB/cByJ": "EFO:0000603", "very long-chain saturated fatty acid measurement": "EFO:0006796", "CD4-intermediate, CD8-positive double-positive thymocyte": "CL:0002430", "Hypomyelination with brain stem and spinal cord involvement and leg spasticity": "Orphanet:363412", "Genetic chronic primary adrenal insufficiency": "Orphanet:101960", "Rare genetic gynecological and obstetrical diseases": "Orphanet:183731", "HDL cholesterol change measurement": "EFO:0007805", "immature CD1a-positive dermal dendritic cell": "CL:0002530", "CD4-positive, alpha-beta T cell": "CL:0000624", "L2 larva": "EFO:0002719", "HCC3153": "EFO:0001179", "HUES64": "EFO:0007089", "germline genotype": "EFO:0004973", "B10.NOD_H2g7_Idd3": "EFO:0002741", "Multiple ventricular septal defects": "Orphanet:99096", "FADD-related immunodeficiency": "Orphanet:306550", "Sudden infant death - dysgenesis of the testes": "Orphanet:168593", "platelet activation": "GO:0030168", "46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue": "Orphanet:98086", "Syndrome with hypoparathyroidism": "Orphanet:181402", "Stomach Volvulus": "EFO:1001852", "3-(indol-3-yl)lactate {http": "CHEBI:17282", "Thyroid hypoplasia": "Orphanet:95720", "Hereditary orotic aciduria": "Orphanet:30", "Saccharomyces paradoxus": "NCBITaxon:27291", "Lissencephaly with cerebellar hypoplasia type A": "Orphanet:100011", "pancreatic A cell": "CL:0000171", "Microalbuminuria": "HP:0012594", "Thiamine-responsive encephalopathy": "Orphanet:199348", "breast tumor luminal": "EFO:0000306", "G402": "EFO:0002180", "Non-eruption of teeth - maxillary hypoplasia - genu valgum": "Orphanet:2972", "Cyanothece sp. ATCC 51142": "NCBITaxon:43989", "Pfeiffer syndrome type 2": "Orphanet:93259", "3T3-L1": "EFO:0001084", "Fanconi anemia": "Orphanet:84", "dorsomedial neurosecretory cell": "FBbt:00004011", "iPS-15b": "EFO:0007102", "Urocanic aciduria": "Orphanet:210128", "Colorectal Gastrointestinal Stromal Tumor": "EFO:1000192", "Limb overgrowth": "Orphanet:294953", "Spondyloepimetaphyseal dysplasia - hypotrichosis": "Orphanet:168443", "Kit-positive, Sca1-positive common lymphoid progenitor": "CL:0001025", "CME-W2": "EFO:0005744", "Vulpes vulpes": "NCBITaxon:9627", "granulosa cell": "CL:0000501", "RiboMeth-seq": "EFO:0008892", "NCI-H2122": "EFO:0002279", "cardiac stress biomarker measurement": "EFO:0008471", "(1S,2R)-5-methoxy-1-methyl-2-(propylamino)tetralin hydrochloride": "CHEBI:64115", "BICR 10": "EFO:0006540", "undisturbed flow regions": "EFO:0002749", "tissue modifier": "EFO:0001647", "Zalophus californianus": "NCBITaxon:9704", "GM17816 {http": "CLO:0016509", "Strelkovimermis": "NCBITaxon:382539", "Mt-0": "EFO:0006962", "CLN13 disease": "Orphanet:352709", "pyelocystitis": "EFO:1001835", "Omodysplasia": "Orphanet:2733", "androgenetic alopecia": "EFO:0004191", "Candida dubliniensis": "NCBITaxon:42374", "Disorder of copper metabolism": "Orphanet:309839", "Lobar holoprosencephaly": "Orphanet:93924", "MT10430": "EFO:0005493", "Ring chromosome 18": "Orphanet:1442", "Piebald trait - neurologic defects": "Orphanet:2885", "X-linked intellectual disability - hypogonadism - ichthyosis - obesity - short stature": "Orphanet:85331", "ACTH-Producing Pituitary Gland Adenoma": "EFO:1000066", "CS57628": "EFO:0000044", "CS57871": "EFO:0000151", "radiotherapy-induced pemphigus": "EFO:0008608", "OCIA domain-containing protein 1 measurement": "EFO:0008252", "Atelosteogenesis type III": "Orphanet:56305", "Insecta {http": "NCBITaxon:50557", "SS149": "EFO:0004089", "Gilbert syndrome": "EFO:0005556", "Partial duplication of the short arm of chromosome X": "Orphanet:263775", "UMI Method": "EFO:0008980", "Corneal astigmatism": "EFO:1002040", "interaction with other organism via secreted substance involved in symbiotic interaction": "GO:0052047", "6p22 microdeletion syndrome": "Orphanet:251046", "LEOPARD syndrome": "Orphanet:500", "HT3": "EFO:0002204", "response to iloperidone": "GO:0036287", "limited iron regimen {http": "EO:0001047", "Autosomal recessive Emery-Dreifuss muscular dystrophy": "Orphanet:98855", "Hemolytic anemia due to red cell pyruvate kinase deficiency": "Orphanet:766", "mesonephric adenocarcinoma": "EFO:0006719", "DMS53": "EFO:0002165", "B-cell non-Hodgkins lymphoma": "EFO:1001938", "Glycogen storage disease due to phosphorylase kinase deficiency": "Orphanet:370", "LN-229": "EFO:0006637", "LP.14 fourteen leaves visible stage": "PO:0007085", "Auriculocondylar syndrome": "Orphanet:137888", "occipital lateral line neuromast": "UBERON:2001025", "magnesium measurement": "EFO:0004845", "explosive role": "CHEBI:63490", "Rare isolated myopia": "Orphanet:98619", "diphtheria": "EFO:0005549", "Testicular Embryonal Carcinoma": "EFO:1000565", "Myopathy with eye involvement": "Orphanet:98689", "Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin": "Orphanet:400011", "Iodine Deficiency Hypothyroidism": "EFO:0008614", "Hereditary cerebral hemorrhage with amyloidosis, Iowa type": "Orphanet:324708", "Fibrodysplasia ossificans progressiva": "Orphanet:337", "alpha-adrenergic antagonist": "CHEBI:37890", "persistent Staphylococcus aureus carrier status": "EFO:0007757", "mucocutaneous lymph node syndrome": "EFO:0004246", "Fanconi anemia complementation group G": "EFO:0009046", "paraventricular nucleus": "UBERON:0001930", "NOD.scid": "EFO:0002740", "Progressive cone dystrophy": "Orphanet:1871", "lung adenocarcinoma grade": "EFO:0005620", "Erysipelothrix rhusiopathiae infectious disease": "EFO:1000928", "brachial plexus neuropathy": "EFO:1000844", "Cervical Adenosquamous Carcinoma": "EFO:1000162", "mushroom body": "UBERON:0001058", "Panc 04.03": "EFO:0006468", "Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus": "Orphanet:2579", "Autosomal dominant medullary cystic kidney disease with or without hyperuricemia": "Orphanet:34149", "Leishmania braziliensis": "NCBITaxon:5660", "familial cardiomyopathy": "EFO:0002945", "3-hydroxyisobutyrate {http": "CHEBI:11805", "Qualitative or quantitative defects of tropomyosin": "Orphanet:284790", "viral encephalitis": "EFO:0007538", "carotenoid measurement": "EFO:0004737", "intracellular membrane-bounded organelle": "GO:0043231", "mouth mucous membrane leukoplakia": "EFO:0006884", "antibody": "EFO:0000264", "concentrated": "PATO:0001159", "word reading": "EFO:0005300", "acute inflammatory response": "GO:0002526", "C-C motif chemokine 19 measurement": "EFO:0008047", "endometriosis": "EFO:0001065", "platelet glycoprotein 4 measurement": "EFO:0008262", "Hypoplastic tibiae - postaxial polydactyly": "Orphanet:3332", "alpha-1-antichymotrypsin complex measurement": "EFO:0008018", "kidney amyloid deposition measurement": "EFO:0008371", "antiprogestin": "EFO:0002673", "MALBAC": "EFO:0008793", "Cerebro-oculo-nasal syndrome": "Orphanet:66625", "Partial deletion of the short arm of chromosome 19": "Orphanet:261983", "Coturnix japonica": "NCBITaxon:93934", "chloroquine": "CHEBI:3638", "posttemporal": "UBERON:2000549", "ureterolithiasis": "EFO:1001228", "Dyspnea {http": "HP:0002094", "Niemann-Pick disease type C, severe perinatal form": "Orphanet:216972", "cell type comparison design": "EFO:0001745", "Fusarium graminearum": "NCBITaxon:5518", "dopamine agonist": "CHEBI:51065", "Lateral facial cleft": "Orphanet:141269", "CS57811": "EFO:0000125", "oleic acid": "CHEBI:16196", "drug use measurement": "EFO:0007010", "Rare hemorrhagic disorder due to a constitutional thrombocytopenia": "Orphanet:275729", "ATC Code G Genito-urinary system and sex hormones": "EFO:0005638", "Isolated anterior cervical hypertrichosis": "Orphanet:3387", "Tricarboxylic acid cycle disorder": "Orphanet:254749", "Pinus pinaster": "NCBITaxon:71647", "facial dermatosis": "EFO:1000698", "C24 ecotype": "EFO:0006987", "GLP-1-stimulated insulin response": "EFO:0008531", "cathasterone": "CHEBI:23057", "decidua basalis": "UBERON:0000453", "crus helix expression": "EFO:0007672", "oligoastrocytoma": "EFO:0000630", "4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone": "CHEBI:32692", "Ectodermal dysplasia, Berlin type": "Orphanet:1816", "Fusarium avenaceum": "NCBITaxon:40199", "head mesenchyme": "UBERON:0005253", "SHEF-3": "EFO:0005455", "phospholipid measurement": "EFO:0004639", "response to dalcetrapib": "EFO:0006916", "Griscelli disease type 1": "Orphanet:79476", "intestinal polyp": "EFO:0003855", "Monosomy 13q34": "Orphanet:96168", "3q26q27 microdeletion syndrome": "Orphanet:356947", "drinking behavior": "EFO:0004315", "urothelial carcinoma": "EFO:0008528", "Smart-seq2 protocol": "EFO:0008442", "restriction digest": "EFO:0004179", "array control genomic DNA": "EFO:0005436", "GM17756 {http": "CLO:0016554", "Clostridium acetobutylicum": "NCBITaxon:1488", "PC-3": "EFO:0002074", "Progressive external ophthalmoplegia - myopathy - emaciation": "Orphanet:352447", "Gestational trophoblastic neoplasm": "Orphanet:59305", "thrombus formation measurement": "EFO:0007615", "Streptomyces cattleya": "NCBITaxon:29303", "glycosyl compound metabolic process": "GO:1901657", "Theiler stage 22": "EFO:0002585", "tinea": "EFO:0007510", "tracheal primordium": "UBERON:6005037", "Humero-radial synostosis": "Orphanet:3265", "mitotic cell cycle": "GO:0000278", "endocardial fibroelastosis": "EFO:0007251", "bladder neck obstruction": "EFO:1000840", "haustorium": "BTO:0000515", "adult-onset Still's disease": "EFO:0007135", "hair morphology measurement": "EFO:0007821", "PA-TU-8902": "EFO:0006729", "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation": "Orphanet:280293", "Epileptic encephalopathy {http": "HP:0200134", "amikacin": "CHEBI:2637", "commensal Bacteroidaceae infectious disease": "EFO:1000872", "IgE plasmablast": "CL:0000950", "normal": "PATO:0000461", "protein localization": "GO:0008104", "HCC0012": "EFO:0006416", "atrophic macular degeneration": "EFO:1001492", "Small Intestinal Tubular Adenoma": "EFO:1000538", "megaspore": "CL:0000250", "parietal cell": "CL:0000162", "Orofacial clefting syndrome": "Orphanet:139039", "vagal ganglion 2": "UBERON:2001303", "HFL1": "EFO:0005368", "interleukin 18 measurement": "EFO:0004581", "IgA memory B cell": "CL:0000973", "influenza A severity measurement": "EFO:0007743", "digit": "UBERON:0002544", "Thoracolumbosacral spina bifida aperta": "Orphanet:268384", "Constitutional hemolytic anemia due to acanthocytosis": "Orphanet:98366", "pulmonary plasma cell granuloma": "EFO:1001135", "Birdshot chorioretinopathy": "Orphanet:179", "Minimal pigment oculocutaneous albinism type 1": "Orphanet:352734", "OVSAHO": "EFO:0006727", "JIMT-1": "EFO:0005388", "Ehlers-Danlos syndrome, kyphoscoliotic and deafness type": "Orphanet:300179", "langerin-negative dermal  dendritic cell": "CL:0002459", "Lissencephaly due to LIS1 mutation": "Orphanet:95232", "46,XY partial gonadal dysgenesis": "Orphanet:251510", "3-dehydro-6-deoxoteasterone": "CHEBI:20710", "milligram per day": "EFO:0004419", "Disorder of urea cycle metabolism and ammonia detoxification": "Orphanet:79167", "Congenital entropion": "Orphanet:98568", "GM08928 {http": "CLO:0011237", "Familial isolated hypoparathyroidism": "Orphanet:2238", "JHH-7": "EFO:0006603", "central core myopathy": "EFO:1000855", "Stereotypy {http": "HP:0000733", "B140P": "EFO:0002043", "Hereditary myopathy with lactic acidosis due to ISCU deficiency": "Orphanet:43115", "genome": "EFO:0004420", "Lung Inflammatory Myofibroblastic Tumor": "EFO:1000333", "interleukin 9 measurement": "EFO:0008192", "acinar cell carcinoma": "EFO:0000216", "Immunodeficiency due to absence of thymus": "Orphanet:331220", "Trichodermodysplasia - dental alterations": "Orphanet:3353", "birth measurement": "EFO:0006921", "PARE-Seq": "EFO:0008846", "Corallus": "NCBITaxon:51859", "GM17237 {http": "CLO:0014330", "Pyruvate kinase hyperactivity": "EFO:0005840", "siRNA library": "EFO:0007564", "Guanarito virus": "NCBITaxon:45219", "retinal cell": "CL:0009004", "Plum pox virus": "NCBITaxon:12211", "word list delayed recall measurement": "EFO:0006805", "derived mass unit": "EFO:0001703", "DPAGT1-CDG": "Orphanet:86309", "ILSXISS24/TejJ": "EFO:0002980", "Arnold-Chiari malformation type I": "Orphanet:268882", "Faciocardiorenal syndrome": "Orphanet:1973", "laterality measurement": "EFO:0008372", "Okihiro syndrome": "Orphanet:93293", "vanillylmandelate {http": "CHEBI:27622", "O-acetylhomoserine {http": "CHEBI:7671", "oppositional defiant disorder measurement": "EFO:0007679", "Autosomal recessive spastic paraplegia type 60": "Orphanet:401800", "ovarian serous cystadenocarcinoma": "EFO:1000043", "rosette leaf {http": "PO:0000014", "Thyroid Gland Oncocytic Follicular Carcinoma": "EFO:1000592", "glial brain cell": "EFO:1001464", "insulin-like growth factor-binding protein 7 measurement": "EFO:0008161", "Abnormality of the digestive system": "HP:0025031", "filament": "PO:0009067", "splenic marginal zone macrophage": "CL:0000872", "Sulfolobus solfataricus P2": "NCBITaxon:273057", "Congenital pseudoarthrosis of the fibula": "Orphanet:295022", "Pinus sylvestris": "NCBITaxon:3349", "Sporadic infantile bilateral striatal necrosis": "Orphanet:225147", "Coxoauricular syndrome": "Orphanet:1508", "Ureter Carcinoma": "EFO:1000609", "levetiracetam": "CHEBI:6437", "auditory system disease": "EFO:1001455", "Fibular hemimelia, unilateral": "Orphanet:295081", "Hibiscus chlorotic ringspot virus infection": "EFO:0000782", "incontinentia pigmenti achromians": "EFO:1000716", "Brown Norway": "EFO:0005290", "aggressive behavior": "EFO:0003015", "serine/threonine-protein kinase 17B measurement": "EFO:0008281", "GM17833 {http": "CLO:0016519", "Roseolovirus infectious disease": "EFO:0007474", "Staphylococcus epidermidis": "NCBITaxon:1282", "coffee consumption": "EFO:0004330", "Neonatal glycine encephalopathy": "Orphanet:289857", "Autosomal recessive limb-girdle muscular dystrophy type 2A": "Orphanet:267", "Colon Mucosa-Associated Lymphoid Tissue Lymphoma": "EFO:1000186", "Selaginella": "NCBITaxon:3246", "genetic modification design": "EFO:0001758", "ML-DmD23": "EFO:0007113", "Vitis amurensis": "NCBITaxon:103351", "vitamin B measurement": "EFO:0004843", "intermediate monocyte": "CL:0002393", "post-operative sign or symptom": "EFO:0005323", "sensory perception of taste": "GO:0050909", "Spinocerebellar ataxia type 4": "Orphanet:98765", "MEL cell line": "EFO:0003971", "pericyte": "CL:0000669", "Maternally-inherited spastic paraplegia": "Orphanet:320360", "Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome": "EFO:0009009", "Neonatal adrenoleukodystrophy": "Orphanet:44", "Hypomyelination - hypogonadotropic hypogonadism - hypodontia": "Orphanet:88637", "Congenital absence of both forearm and hand": "Orphanet:294979", "in vitro transcription": "EFO:0009013", "Saethre-Chotzen syndrome": "Orphanet:794", "age at breast cancer diagnosis": "EFO:0005603", "GM17268 {http": "CLO:0013177", "multinucleated giant cell": "CL:0000647", "carbaryl": "CHEBI:3390", "Rhabditinae": "NCBITaxon:55887", "Slender bone dysplasia": "Orphanet:93440", "c3d": "EFO:0008543", "Distal myopathy": "Orphanet:599", "Yarrowia lipolytica": "NCBITaxon:4952", "dyspepsia": "EFO:0008533", "YCC1": "EFO:0002876", "tartrate(1-) {http": "CHEBI:35397", "interleukin 7 measurement": "EFO:0008189", "Locusta migratoria manilensis": "NCBITaxon:229990", "Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement": "Orphanet:352309", "Proteinuria": "HP:0000093", "proximal": "EFO:0001661", "Qualitative or quantitative defects of telethonin": "Orphanet:209056", "OE33": "EFO:0002310", "brachiocephalic artery": "UBERON:0001529", "Xp22.3 microdeletion syndrome": "Orphanet:1643", "leukoplakia of penis": "EFO:1001015", "3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form": "Orphanet:79351", "Epstein-Barr virus infection": "EFO:0000769", "recombination rate": "EFO:0004863", "Frey Syndrome": "EFO:1000940", "herbicide": "CHEBI:24527", "Spondyloepimetaphyseal dysplasia, Irapa type": "Orphanet:93351", "HH": "EFO:0002194", "Geospiza scandens": "NCBITaxon:48886", "Coats disease": "Orphanet:190", "rotenone": "CHEBI:28201", "CS57692": "EFO:0000062", "HSD10 disease, neonatal type": "Orphanet:391457", "iodoform": "CHEBI:37758", "head mesenchyme from mesoderm": "UBERON:0006904", "pollen sperm cell {http": "PO:0025121", "Rare palpebral disease": "Orphanet:98560", "microsecond": "UO:0000029", "Familial drusen": "Orphanet:75376", "site": "BFO:0000029", "regeneration epithelium": "ZFA:0001389", "Pseudo-seq": "EFO:0008872", "Angiomatous Meningioma": "EFO:1000086", "NCI-H2452": "EFO:0006680", "farm exposure measurement": "EFO:0008362", "Vitamin B12-unresponsive methylmalonic acidemia": "Orphanet:27", "IM-95": "EFO:0006446", "TruePrime": "EFO:0008977", "hepatitis C induced liver cirrhosis": "EFO:0005129", "stromal cell-derived factor 1 alpha measurement": "EFO:0008293", "Spondyloperipheral dysplasia - short ulna": "Orphanet:1856", "SK-MM-1": "EFO:0005457", "3-aminoisobutyrate {http": "CHEBI:49096", "Richieri Costa-Pereira syndrome": "Orphanet:3102", "Eosinophilia-Myalgia Syndrome": "EFO:1001316", "tricuspid valve stenosis": "EFO:0007525", "Alagille syndrome due to a NOTCH2 point mutation": "Orphanet:261629", "Piscirickettsiaceae Infections": "EFO:1001397", "D,L-2-hydroxyglutaric aciduria": "Orphanet:356978", "Lactobacillus panis": "NCBITaxon:47493", "field study": "EO:0007256", "plastid membrane": "GO:0042170", "Fried syndrome": "Orphanet:85335", "Spondylodysplastic dysplasia": "Orphanet:93434", "median fin fold": "UBERON:2000040", "CS57512": "EFO:0000003", "Paraganglioma": "EFO:1000453", "(+)-abscisic acid": "CHEBI:2365", "MHC-II-negative classical monocyte": "CL:0002469", "area": "EFO:0001696", "oral squamous cell carcinoma": "EFO:0000199", "Brachydactyly - elbow wrist dysplasia": "Orphanet:1275", "Escherichia fergusonii": "NCBITaxon:564", "Dysplasia in Ulcerative Colitis": "EFO:1000226", "vascular sarcoma": "EFO:0003967", "Alpers syndrome": "Orphanet:726", "Myhre syndrome": "Orphanet:2588", "primordial vasculature": "UBERON:0014903", "Familial benign flecked retina": "Orphanet:363989", "Ruegeria pomeroyi DSS-3": "NCBITaxon:246200", "Multiple epiphyseal dysplasia type 5": "Orphanet:93311", "chondroblastoma": "EFO:0000331", "GP5d": "EFO:0006576", "opercle": "UBERON:2000250", "Camptodactyly - tall stature - scoliosis - hearing loss": "Orphanet:85164", "Dermatitis, Perioral": "EFO:1001305", "Autosomal dominant cerebellar ataxia type 1": "Orphanet:94145", "carpel {http": "PO:0009030", "Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome": "Orphanet:369939", "latanoprost free acid": "CHEBI:63925", "nucleus accumbens": "UBERON:0001882", "Urothelial Dysplasia": "EFO:1000611", "Shigella sonnei": "NCBITaxon:624", "Coenzyme Q10 deficiency": "Orphanet:35656", "(R)-2-hydroxypalmitate {http": "CHEBI:75927", "Lactobacillus reuteri F275": "NCBITaxon:299033", "larval day 6": "EFO:0001306", "typhoid fever": "EFO:0006789", "Bohring-Opitz syndrome": "Orphanet:97297", "Familial retinal arterial macroaneurysm": "Orphanet:284247", "Congenital factor II deficiency": "Orphanet:325", "spermatocele": "EFO:1001189", "MKN28": "EFO:0002831", "inferior vagus X ganglion {http": "UBERON:0005363", "ferric ammonium citrate": "CHEBI:31604", "prepuce of penis": "UBERON:0001332", "hypaphorine {http": "CHEBI:5832", "Partial duplication of the long arm of chromosome 1": "Orphanet:262833", "GM14509 {http": "CLO:0031609", "N1 lymph node stage": "EFO:0004933", "GM14582 {http": "CLO:0031666", "sRNA-Seq": "EFO:0008947", "sex design": "EFO:0001752", "HCC1428": "EFO:0001171", "cystadenocarcinoma": "EFO:0006387", "sRAGE measurement": "EFO:0007622", "Abnormality of nitrogen compound homeostasis": "HP:0004364", "Machupo virus": "NCBITaxon:11628", "Autosomal recessive spastic ataxia of Charlevoix-Saguenay": "Orphanet:98", "Puerperal Infection": "EFO:1001407", "Tendon Sheath Fibroma": "EFO:1000561", "Porokeratotic eccrine ostial and dermal duct nevus": "Orphanet:166286", "Disorder of phenylalanin or tyrosine metabolism": "Orphanet:79190", "Overgrowth - macrocephaly - facial dysmorphism": "Orphanet:137634", "megacolon": "HP:0002251", "Distal monosomy 7q36": "Orphanet:1636", "Microcephaly - seizures - intellectual disability - heart disease": "Orphanet:2519", "polyp": "EFO:0000662", "Adamantinomatous Craniopharyngioma": "EFO:1000069", "Gyrate atrophy of choroid and retina": "Orphanet:414", "Coloboma of iris": "Orphanet:98944", "pregnancy": "EFO:0002950", "Isobutyryl-CoA dehydrogenase deficiency": "Orphanet:79159", "Reticular dystrophy of the retinal pigment epithelium": "Orphanet:99002", "JHH-2": "EFO:0006600", "dorsolateral prefrontal cortex functional measurement": "EFO:0008358", "double negative memory B cell": "CL:0000981", "blood pressure change measurement": "EFO:0006943", "Bos indicus": "NCBITaxon:9915", "CS57515": "EFO:0000004", "Charcot-Marie-Tooth disease type 4B1": "Orphanet:99955", "Ptosis - syndactyly - learning difficulties": "Orphanet:238766", "anti-centromere-antibody-positive systemic scleroderma": "EFO:0008536", "targeted mutation": "EFO:0004019", "alcohol consumption measurement": "EFO:0007878", "Humero-radial synostosis, bilateral": "Orphanet:295211", "Roberts syndrome": "Orphanet:3103", "Syndromic nail anomaly": "Orphanet:79370", "Fatal multiple mitochondrial dysfunction syndrome": "Orphanet:289573", "Microcephaly - brain defect - spasticity - hypernatremia": "Orphanet:2523", "asymmetric dimethylarginine": "CHEBI:17929", "COG8-CDG": "Orphanet:95428", "Intellectual disability - hypotonia - spasticity - sleep disorder": "Orphanet:356996", "Split foot, bilateral": "Orphanet:295126", "Upper thoracic spina bifida cystica": "Orphanet:268770", "Autosomal dominant childhood-onset cortical cataract": "Orphanet:306561", "Dahl salt-resistant": "EFO:0001349", "GM17163 {http": "CLO:0013996", "Pu-seq": "EFO:0008875", "2-butoxyethanol": "CHEBI:63921", "WI38": "EFO:0001260", "Umbilical cord ulceration - intestinal atresia": "Orphanet:3405", "Streptococcus pyogenes M49 591": "NCBITaxon:294934", "AIDS dementia": "EFO:0002608", "ncRNA": "SO:0000655", "Hodgkins lymphoma": "EFO:0000183", "ear": "UBERON:0001690", "Oculomotor palsy": "Orphanet:98685", "Cystic leukoencephalopathy without megalencephaly": "Orphanet:85136", "UACC-62": "EFO:0005377", "Manduca sexta": "NCBITaxon:7130", "cot filtration for highly repetitive genomic DNA": "EFO:0004173", "Facial dysmorphism - immunodeficiency - livedo - short stature": "Orphanet:352712", "myofascial pain syndrome": "EFO:1001054", "disease cell type": "EFO:0005934", "Langer-Giedion syndrome": "Orphanet:502", "647V": "EFO:0002098", "mandibular muscle": "UBERON:0011648", "cinidon ethyl": "CHEBI:63927", "Metachromatic leukodystrophy": "Orphanet:512", "schizophrenia": "EFO:0000692", "Spastic paraplegia-optic atrophy-neuropathy syndrome": "Orphanet:320406", "Adducted thumbs - arthrogryposis, Christian type": "Orphanet:2952", "GM17246 {http": "CLO:0014416", "S49": "EFO:0001234", "appendicular skeleton": "UBERON:0002091", "erythrocyte count": "EFO:0004305", "discretized differential expression": "EFO:0004034", "Magnetospirillum magneticum AMB-1": "NCBITaxon:342108", "bone quantitative ultrasound measurement": "EFO:0004514", "Gray platelet syndrome": "Orphanet:721", "N-methyl-N'-nitro-N-nitrosoguanidine": "CHEBI:21759", "purine nucleoside monophosphate biosynthetic process": "GO:0009127", "Beckwith-Wiedemann syndrome due to imprinting defect of 11p15": "Orphanet:231117", "gallstones": "EFO:0004210", "Theiler stage 6": "EFO:0004398", "AG11364 {http": "CLO:0021597", "bird fancier's lung": "EFO:0007170", "Ataxia - tapetoretinal degeneration": "Orphanet:1178", "Columba livia": "NCBITaxon:8932", "nucleated thrombocyte": "CL:0000762", "Parotid Gland Carcinoma": "EFO:1000460", "Hereditary palmoplantar keratoderma": "Orphanet:79357", "NTera2": "EFO:0002959", "uterine leiomyosarcoma": "EFO:1001974", "GM14477 {http": "CLO:0031531", "thrombocytopenia": "HP:0001873", "Low-set ears {http": "HP:0000369", "dietary potassium intake measurement": "EFO:0008470", "Partial deletion of the short arm of chromosome 11": "Orphanet:261947", "array": "EFO:0002698", "M059J": "EFO:0005697", "Stenocarpella maydis": "NCBITaxon:238245", "membrane-enclosed lumen": "GO:0031974", "Propionic acidemia": "Orphanet:35", "circadian rhythm": "EFO:0004354", "sporadic amyotrophic lateral sclerosis": "EFO:0001357", "GM17273 {http": "CLO:0013197", "Bl-1": "EFO:0005173", "Brachydactyly type A4": "Orphanet:93394", "NCI-H28": "EFO:0006686", "JURKAT E-6.1 cell": "BTO:0001948", "neuroblast (sensu Vertebrata)": "CL:0000337", "reproductive process": "GO:0000003", "Glycoproteinosis": "Orphanet:309279", "forced expiratory volume": "EFO:0004314", "gemfibrozil": "CHEBI:5296", "Grade III Prostatic Intraepithelial Neoplasia": "EFO:1000283", "Leukocyte adhesion deficiency type I": "Orphanet:99842", "rosette growth complete stage": "PO:0007078", "toxascariasis": "EFO:0007515", "lactose intolerance adult type": "EFO:1000063", "Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes": "EFO:1000329", "epibranchial 5": "ZFA:0001244", "AVL induced bursal lymphoma": "EFO:0005923", "histidine {http": "CHEBI:27570", "male breast carcinoma": "EFO:0006861", "Autosomal dominant spastic paraplegia type 37": "Orphanet:171612", "Low Grade Vulvar Intraepithelial Neoplasia": "EFO:1000330", "azithromycin": "CHEBI:2955", "Dentin dysplasia type II": "Orphanet:99791", "monolayer-surrounded lipid storage body": "GO:0012511", "1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid": "CHEBI:50138", "extraction protocol": "EFO:0000490", "colony forming unit per milliliter": "UO:0000213", "Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome": "Orphanet:363429", "aspartate(1-) {http": "CHEBI:35391", "Congenital cataract - ichthyosis": "Orphanet:1376", "centimeter": "UO:0000015", "Caulobacter crescentus CB15": "NCBITaxon:190650", "serum alanine aminotransferase measurement": "EFO:0004735", "height growth measurement": "EFO:0005201", "Acute Leukemia": "EFO:1000068", "cellular response to stimulus": "GO:0051716", "Ehlers-Danlos syndrome with periventricular heterotopia": "Orphanet:82004", "PAIR": "EFO:0008841", "seminal root {http": "PO:0000046", "Acheiria": "Orphanet:294983", "Dysostosis of genetic origin with limb anomaly as a major feature": "Orphanet:404571", "GM12236": "EFO:0001143", "logarithmic phase culture": "BTO:0001903", "Autosomal dominant optic atrophy": "Orphanet:98672", "Polysomy of X chromosome": "Orphanet:263723", "Qualitative or quantitative defects of delta-sarcoglycan": "Orphanet:207070", "Oculoauriculofrontonasal syndrome": "Orphanet:398156", "Mycobacterium avium subsp. paratuberculosis": "NCBITaxon:1770", "risperidone": "CHEBI:8871", "Congenital absence of thigh and lower leg with foot present": "Orphanet:294977", "Congenital eyelid retraction": "Orphanet:99176", "superficial blastomere": "ZFA:0001484", "Mixed Cell Uveal Melanoma": "EFO:1000380", "HCC1395": "EFO:0002185", "Male infertility with spermatogenesis disorder due to single gene mutation": "Orphanet:399786", "Bacteria": "NCBITaxon:2", "Qualitative or quantitative defects of fukutin": "Orphanet:207122", "interleukin (Mus musculus)": "EFO:0003792", "2,4-dinitrophenol": "CHEBI:42017", "Genetic frontotemporal degeneration with dementia": "Orphanet:276061", "Capsicum annuum": "NCBITaxon:4072", "Lissencephaly with cerebellar hypoplasia": "Orphanet:86823", "Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency": "Orphanet:276598", "premature chromatid separation trait": "EFO:0009077", "Mohr-Tranebjaerg syndrome": "Orphanet:52368", "N-acetyl-L-glutamate(2-) {http": "CHEBI:44337", "host": "EFO:0000532", "Autosomal recessive cerebellar ataxia - blindness - deafness": "Orphanet:95433", "mature conventional dendritic cell": "CL:0000841", "interleukin 13 measurement": "EFO:0008171", "Obesity due to congenital leptin resistance": "Orphanet:179490", "Henipavirus infectious disease": "EFO:0007300", "CS57586": "EFO:0000023", "teratozoospermia": "EFO:0002625", "Agouti-related protein measurement": "EFO:0008016", "meningococcal infection": "EFO:0004249", "estrogen": "CHEBI:50114", "Retinohepatoendocrinologic syndrome": "Orphanet:3087", "Kasumi2": "EFO:0002224", "immature CD8_alpha-low Langerhans cell": "CL:0001018", "Primary hypomagnesemia with secondary hypocalcemia": "Orphanet:30924", "plastid envelope": "GO:0009526", "GM17235 {http": "CLO:0014334", "restless legs syndrome": "EFO:0004270", "Immunodeficiency due to a late component of complements deficiency": "Orphanet:169150", "Ramos": "EFO:0002077", "lung disease": "EFO:0003818", "Therapy-Related Myeloid Neoplasm": "EFO:1000575", "lymphatic vessel": "UBERON:0001473", "sebaceous gland disease": "EFO:1000763", "hydroxy-leucine measurement": "EFO:0005276", "Eyelid border anomaly": "Orphanet:98564", "Spinocerebellar ataxia type 20": "Orphanet:101110", "lipopolysaccharide": "CHEBI:16412", "Polyploidy": "Orphanet:96321", "Muscular glycogenosis": "Orphanet:206959", "response to interferon": "EFO:0007859", "eye neoplasm": "EFO:0003824", "Gray": "UO:0000134", "pars planitis": "EFO:1001088", "Isolated Dandy-Walker malformation without hydrocephalus": "Orphanet:269215", "Maxillary Sinus Adenoid Cystic Carcinoma": "EFO:1000365", "nevus count": "EFO:0004632", "Glutathione synthetase deficiency with 5-oxoprolinuria": "Orphanet:289846", "mandibular cancer": "EFO:0007356", "brain neoplasm": "EFO:0003833", "Hereditary sclerosing poikiloderma, Weary type": "Orphanet:221039", "Other immunodeficiency syndrome due to defects in adaptive immunity": "Orphanet:331217", "esophageal endoderm": "EFO:0002575", "Double outlet right ventricle, Fallot type": "Orphanet:99043", "Spinocerebellar ataxia - dysmorphism": "Orphanet:1185", "Disorder of lysosomal-related organelles": "Orphanet:309340", "native plant cell {http": "PO:0025606", "Schneckenbecken dysplasia": "Orphanet:3144", "multipotent stem cell": "CL:0000048", "interleukin 8 measurement": "EFO:0008191", "Thermoanaerobacter sp. X514": "NCBITaxon:399726", "Myoclonus-dystonia syndrome": "Orphanet:36899", "amphotericin B": "CHEBI:2682", "Marin-Amat syndrome": "Orphanet:101104", "orotic acid": "CHEBI:16742", "Congenital alpha2 antiplasmin deficiency": "Orphanet:79", "HCC202": "EFO:0001176", "Staphylococcus aureus subsp. aureus Mu50": "NCBITaxon:158878", "Zea mays subsp. parviglumis": "NCBITaxon:76912", "Martuba ecotype": "EFO:0006960", "GM17159 {http": "CLO:0013964", "3P-Seq": "EFO:0008644", "posterior midgut proper primordium": "EFO:0003370", "T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta": "Orphanet:169160", "Cloverleaf skull - multiple congenital anomalies": "Orphanet:93267", "Aspartylglucosaminuria": "Orphanet:93", "CS57520": "EFO:0000005", "green house study": "EO:0007248", "Autosomal dominant nail dysplasia": "Orphanet:79153", "Genetic macular dystrophy": "Orphanet:98664", "soluble P-selectin measurement": "EFO:0004519", "Familial hypodysfibrinogenemia": "Orphanet:248408", "Fuchs endothelial corneal dystrophy": "Orphanet:98974", "AGO-CLIP": "EFO:0008651", "response to methylphenidate": "GO:0036271", "Carnitine palmitoyl transferase 1A deficiency": "Orphanet:156", "Ebstein anomaly": "EFO:0007244", "cell component comparison design": "EFO:0001743", "pulmonary subvalvular stenosis": "EFO:1001137", "Rare genetic respiratory disease": "Orphanet:156610", "CLN4B disease": "Orphanet:228343", "Salmonella enterica subsp. enterica serovar Java": "NCBITaxon:224729", "polylysine substrate coating": "EFO:0005071", "blastula 512-cell": "EFO:0001278", "adolescent idiopathic scoliosis": "EFO:0005423", "albumin": "EFO:0005128", "Pneumonia, Aspiration": "EFO:1001399", "splenocyte": "CL:2000074", "HCC1195": "EFO:0005371", "body weights and measures": "EFO:0004324", "G\u00c3\u00b3mez-L\u00c3\u00b3pez-Hern\u00c3\u00a1ndez syndrome": "Orphanet:1532", "vascular malformation": "EFO:0006888", "GM14465 {http": "CLO:0031275", "iatrogenic Kaposi's sarcoma": "EFO:0002613", "Arthropoda {http": "NCBITaxon:6656", "N-allyl-1-phenyl-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide": "CHEBI:63978", "HPL1C": "EFO:0006908", "Lethal arthrogryposis - anterior horn cell disease": "Orphanet:53696", "methyl (-)-jasmonate": "CHEBI:15929", "yolk sac": "UBERON:0001040", "R11": "EFO:0002849", "infant": "EFO:0001355", "drug psychosis": "EFO:1000902", "OVCAR4": "EFO:0005442", "Congenital ichthyosis - microcephalus - tetraplegia": "Orphanet:2271", "eccrine acrospiroma": "EFO:1000912", "Mesomelic and rhizo-mesomelic dysplasia": "Orphanet:93438", "St\u00c3\u00bcve-Wiedemann syndrome": "Orphanet:3206", "caryopsis": "EFO:0006814", "CAL851": "EFO:0005359", "Cardiac disease with cataract": "Orphanet:98647", "Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency": "Orphanet:331226", "purine nucleotide metabolic process": "GO:0006163", "SD minus nitrogen": "EFO:0007028", "GRO-seq": "EFO:0005227", "Adult-onset dystonia-parkinsonism": "Orphanet:199351", "cystic, mucinous, and serous neoplasm": "EFO:1000889", "germ cell tumor": "EFO:0000514", "stromal corneal pigmentation": "EFO:1000770", "Crohn's disease": "EFO:0000384", "X-linked Ehlers-Danlos syndrome": "Orphanet:75497", "sensory perception of bitter taste": "GO:0050913", "Braddock syndrome": "Orphanet:52047", "pirinixic acid": "CHEBI:32509", "unit per kilogram": "EFO:0002931", "INC-2 cell": "BTO:0004264", "G61": "EFO:0006410", "idiopathic CD4-positive T-lymphocytopenia": "EFO:0007322", "Leri pleonosteosis": "Orphanet:2900", "ear inflorescence {http": "PO:0020136", "Sporisorium reilianum f. sp. zeae {http": "NCBITaxon:72740", "gene list": "OBI:0000118", "Oscheius myriophila": "NCBITaxon:281680", "GM12043": "EFO:0001132", "ovarian neoplasm": "EFO:0003893", "O-tiglylcarnitine {http": "CHEBI:71179", "Woolly hair - hypotrichosis - everted lower lip - outstanding ears": "Orphanet:1409", "Autosomal ichthyosis syndrome with other associated signs": "Orphanet:281244", "benzo(a)pyrene": "CHEBI:29865", "PHAVER syndrome": "Orphanet:2876", "Tay-Sachs disease": "Orphanet:845", "Cortical pulverulent cataract": "HP:0007780", "Syndromic anorectal malformation": "Orphanet:117573", "villitis": "EFO:0003110", "GM08388 {http": "CLO:0010521", "Glanzmann thrombasthenia": "Orphanet:849", "gestational serum measurement": "EFO:0007964", "Generalized resistance to thyroid hormone": "Orphanet:3221", "lower epidermis": "BTO:0000488", "Spinocerebellar ataxia type 41": "EFO:0009058", "neuropsychological test": "EFO:0003926", "Familial focal epilepsy with variable foci": "Orphanet:98820", "precursor B cell": "CL:0000817", "Thalassiosira pseudonana": "NCBITaxon:35128", "BEN": "EFO:0006537", "bulbar polio": "EFO:0007186", "Acro-cardio-facial syndrome": "Orphanet:2008", "IgD-positive CD38-positive IgG memory B cell": "CL:0002106", "Sertoli Cell-Only Syndrome": "EFO:1001422", "Pulmonary Infarction": "EFO:1001408", "Gyps africanus": "NCBITaxon:43490", "Recurrent infection of the gastrointestinal tract": "HP:0004798", "D-glyceric aciduria": "Orphanet:941", "GM17753 {http": "CLO:0016560", "Benign recurrent intrahepatic cholestasis type 1": "Orphanet:99960", "Telecanthus": "Orphanet:98575", "hindgut proper primordium": "FBbt:00000441", "Ehlers-Danlos syndrome type 11": "Orphanet:2295", "Partial deletion of the long arm of chromosome 20": "Orphanet:262164", "C57BL/10": "EFO:0000604", "Medullomyoblastoma with Myogenic Differentiation": "EFO:1000368", "Late-onset primary lymphedema": "Orphanet:289825", "ONT MinION": "EFO:0008632", "Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency": "Orphanet:90793", "Shewanella oneidensis": "NCBITaxon:70863", "Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA": "Orphanet:254767", "hemojuvelin measurement": "EFO:0008148", "Syndromic renal or urinary tract malformation": "Orphanet:93547", "P wave terminal force measurement": "EFO:0008379", "galactoside 34-L-fucosyltransferase measurement": "EFO:0008136", "binding site identification design": "EFO:0004664", "Nathalie syndrome": "Orphanet:2663", "validation high content screen": "EFO:0007558", "infectious colitis": "EFO:1000035", "hypokalemia": "HP:0002900", "granuloma annulare": "EFO:1000704", "Transitional Cell Carcinoma": "EFO:1000601", "Transitional Meningioma": "EFO:1000602", "chitin octamer": "EFO:0003237", "888-mel": "EFO:0006531", "C-C motif chemokine 1 measurement": "EFO:0008041", "Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency": "Orphanet:325529", "in situ oligo": "EFO:0005073", "endometrial adenosquamous carcinoma": "EFO:1001952", "bed nucleus of stria terminalis": "UBERON:0001880", "Perinatal lethal hypophosphatasia": "Orphanet:247623", "malignant peripheral nerve sheath tumor": "EFO:0000760", "Gordon syndrome": "Orphanet:376", "progranulin measurement": "EFO:0004625", "NCI-H838": "EFO:0002307", "ductal adenocarcinoma": "EFO:0000430", "GM15144 {http": "CLO:0029916", "Rh isoimmunization": "EFO:1001159", "Moniliophthora perniciosa": "NCBITaxon:153609", "ectopterygoid": "UBERON:0011634", "HT144": "EFO:0006443", "atrial heart septal defect": "EFO:1000825", "periapical granuloma": "EFO:1001096", "GM17785 {http": "CLO:0016686", "Cleidocranial dysplasia and isolated cranial ossification defect": "Orphanet:93451", "organism": "OBI:0100026", "Bowing of the long bones {http": "HP:0006487", "Carnosinemia": "Orphanet:1361", "psoriasis": "EFO:0000676", "DB": "EFO:0002158", "Congenital lethal myopathy, Compton-North type": "Orphanet:210163", "Foveal hypoplasia - presenile cataract": "Orphanet:2253", "Ovarian Squamous Cell Carcinoma": "EFO:1000432", "X-linked distal spinal muscular atrophy": "Orphanet:139557", "Angioma serpiginosum": "Orphanet:95429", "Eastern Indian": "EFO:0003158", "brain blood vessel": "UBERON:0003499", "metastasis to lymph node": "EFO:0004906", "CCRFCEM": "EFO:0002128", "CS57783": "EFO:0000117", "phospholipase A2, membrane associated measurement": "EFO:0008259", "Abnormality of the urinary system": "HP:0000079", "host intracellular part": "GO:0033646", "CD94-positive Ly49CI-positive natural killer cell": "CL:0002449", "osteoarthritis, knee": "EFO:0004616", "newborn respiratory distress syndrome": "EFO:1000644", "protein secretion": "GO:0009306", "Parkinson's disease": "EFO:0002508", "GM14455 {http": "CLO:0031256", "urinary 1,3-butadiene measurement": "EFO:0007957", "Primary osteolysis": "Orphanet:93449", "Brachydactyly of toes, bilateral": "Orphanet:295134", "Bacteroides ovatus": "NCBITaxon:28116", "lateral geniculate body": "UBERON:0001926", "MEDNIK syndrome": "Orphanet:171851", "HER2 status": "EFO:0005514", "endocrine tuberculosis": "EFO:1000917", "Extensor tendons of finger anomalies": "Orphanet:3294", "personality trait": "EFO:0004365", "D4 glioblastoma derived primary cell line": "EFO:0002051", "Pseudohypoparathyroidism": "Orphanet:97593", "Autosomal dominant Charcot-Marie-Tooth disease type 2G": "Orphanet:99941", "anti-social behavior": "EFO:0004890", "torsades de pointes": "EFO:0005307", "Short chain acyl-CoA dehydrogenase deficiency": "Orphanet:26792", "Strongylida infectious disease": "EFO:0007500", "Mitochondrial DNA depletion syndrome, hepatocerebrorenal form": "Orphanet:363534", "seed development stage {http": "PO:0001170", "hyperosmotic salinity response": "GO:0042538", "GM1 gangliosidosis": "Orphanet:354", "Bladder Inflammatory Myofibroblastic Tumor": "EFO:1000127", "Genetic skin vascular disorder": "Orphanet:183478", "Montastraea faveolata": "NCBITaxon:48498", "Juvenile sialidosis type 2": "Orphanet:93399", "Mitochondrial non-syndromic sensorineural deafness": "Orphanet:90641", "Raynaud disease": "EFO:1001145", "Oculocutaneous albinism type 7": "Orphanet:352745", "iris cancer": "EFO:1000996", "Venous abnormality": "HP:0002624", "corneo-scleral junction": "UBERON:0006761", "Childhood-onset autosomal recessive myopathy with external ophthalmoplegia": "Orphanet:363677", "Radiation Pneumonitis": "EFO:1001411", "neoplasm": "EFO:0000616", "temperament and character inventory": "EFO:0004825", "platelet distribution width": "EFO:0007984", "Generalized arterial calcification of infancy": "Orphanet:51608", "NCI-H748": "EFO:0002304", "response to high-dose melphalan": "EFO:0006314", "JAR": "EFO:0002211", "Callicebus cupreus": "NCBITaxon:202457", "X-linked Charcot-Marie-Tooth disease type 1": "Orphanet:101075", "F1": "EFO:0007032", "pollen {http": "PO:0025281", "Vitamin B12-unresponsive methylmalonic acidemia type mut0": "Orphanet:289916", "mercury poisoning": "EFO:1001810", "medial geniculate body": "UBERON:0001927", "delta wave measurement": "EFO:0006872", "adrenal gland": "CL:0000336", "endothelial cell of umbilical vein": "CL:0002618", "Disorder of amino acid absorption and transport": "Orphanet:79166", "Palmoplantar keratoderma-deafness syndrome": "Orphanet:2202", "Familial capillary hemangioma": "Orphanet:91415", "PC-1": "EFO:0002842", "Peroxisomal disease": "Orphanet:68373", "ARH77": "EFO:0002111", "oxBS-Seq": "EFO:0008840", "IgG isotype profile measurement": "EFO:0008366", "body weight loss": "EFO:0005245", "boutonneuse fever": "EFO:0007179", "Familial partial lipodystrophy due to AKT2 mutations": "Orphanet:79085", "kynurenine": "EFO:0008530", "VMRC-LCD": "EFO:0006773", "Steroid dehydrogenase deficiency - dental anomalies": "Orphanet:3196", "response to high fat food intake": "EFO:0007684", "corm": "PO:0025355", "Rhamphochromis sp. 'chilingali'": "NCBITaxon:454631", "embryonal rhabdomyosarcoma": "EFO:0000437", "pioglitazone": "CHEBI:8228", "benzene-1,2,4-triol": "CHEBI:16979", "estrogen receptor modulator": "CHEBI:50739", "Hereditary dentin defect": "Orphanet:167759", "Blumeria graminis f. sp. tritici {http": "NCBITaxon:62690", "Hereditary breast cancer": "Orphanet:227535", "Macrocephaly-developmental delay syndrome": "Orphanet:397612", "granulins measurement": "EFO:0008141", "silk gland": "UBERON:0011146", "CS57789": "EFO:0000119", "Lactobacillus reuteri 100-23": "NCBITaxon:349123", "CS57595": "EFO:0000026", "immature T cell": "CL:0002420", "Distal trisomy 18q": "Orphanet:1716", "inflammation": "MP:0001845", "integumental system": "UBERON:0002416", "Muir-Torre syndrome": "Orphanet:587", "Nidovirales infectious disease": "EFO:0007396", "Kostmann syndrome": "Orphanet:99749", "OVKATE": "EFO:0006725", "Tracheo-esophageal fistula - hypospadias": "Orphanet:2042", "GM17103 {http": "CLO:0014898", "Teleopsis quinqueguttata": "NCBITaxon:139650", "octadecanoate {http": "CHEBI:25629", "rhombomere 1 floor plate": "UBERON:0005566", "pancreatic tubular adenocarcinoma": "EFO:0006471", "brain connectivity measurement": "EFO:0005210", "C57BL/6-scid": "EFO:0002743", "status epilepticus": "EFO:0008526", "Partial deletion of the short arm of chromosome 7": "Orphanet:261911", "ChIP-chip by tiling array": "EFO:0002762", "urinary arsenic measurement": "EFO:0004880", "Cataract, Hutterite type": "Orphanet:98987", "Upslanted palpebral fissure {http": "HP:0000582", "QG56": "EFO:0002848", "pneumococcal meningitis": "EFO:1001114", "anterior uveitis": "EFO:1000811", "B-1b B cell": "CL:0000821", "a disintegrin and metalloproteinase with thrombospondin motifs 13": "EFO:0008011", "4475": "EFO:0002808", "Beckwith-Wiedemann syndrome due to 11p15 microdeletion": "Orphanet:231127", "ocular hypertension": "EFO:1001069", "CS57658": "EFO:0000054", "Mytilus californianus": "NCBITaxon:6549", "N2": "EFO:0004028", "Bent bone dysplasia": "Orphanet:93439", "Meningeal Melanocytoma": "EFO:1000370", "Lactococcus garvieae": "NCBITaxon:1363", "HGADFN167": "EFO:0005909", "Caffey disease": "Orphanet:1310", "Blepharophimosis - epicanthus inversus - ptosis": "Orphanet:126", "Primary bone dysplasia with multiple joint dislocations": "Orphanet:93441", "uncultured prokaryote": "NCBITaxon:198431", "Laubry-Pezzi syndrome": "Orphanet:99094", "Lactobacillus paraplantarum": "NCBITaxon:60520", "Craniofacial anomaly with cataract": "Orphanet:98650", "Male infertility due to sperm disorder": "Orphanet:399771", "adrenocortical carcinoma": "EFO:0003093", "impetigo herpetiformis": "EFO:1000715", "X-linked intellectual disability - hypotonia - facial dysmorphism - aggressive behavior": "Orphanet:85329", "Staphylococcus aureus subsp. aureus COL": "NCBITaxon:93062", "Spondylometaphyseal dysplasia, Czarny-Ratajczak type": "Orphanet:370019", "Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation": "EFO:1000361", "organism part": "EFO:0000635", "SW954": "EFO:0002376", "Congenital disorder of glycosylation-related bone disorder": "Orphanet:371195", "renal branch of vagus nerve": "FMA:6670", "oroficial granulomatosis": "EFO:1001820", "Monocytopenia with susceptibility to infections": "Orphanet:228423", "Severe X-linked mitochondrial encephalomyopathy": "Orphanet:238329", "Barcode-Seq": "EFO:0008655", "Familial LCAT deficiency": "Orphanet:79293", "Spondyloepiphyseal dysplasia tarda": "Orphanet:93284", "49,XYYYY syndrome": "Orphanet:99330", "albuminuria": "EFO:0004285", "pro-T cell": "CL:0000827", "LIG4 syndrome": "Orphanet:99812", "Peptic ulcer perforation": "EFO:1001389", "embryonic dorsal epidermis": "FBbt:00005744", "cystathionine {http": "CHEBI:17755", "Rare genetic endocrine disease": "Orphanet:156638", "CCD-29Lu": "EFO:0005365", "osteoarthritis biomarker measurement": "EFO:0005890", "azelaate(2-) {http": "CHEBI:78208", "NCI-H1435": "EFO:0006658", "Ring chromosome 3": "Orphanet:96172", "Cleft lip - retinopathy": "Orphanet:1995", "aspirin hydrolysis measurement": "EFO:0005211", "Progressive myoclonic epilepsy type 6": "Orphanet:280620", "mesenchyme derived from head neural crest": "UBERON:0007213", "Autosomal dominant Larsen syndrome": "Orphanet:503", "Huntington disease": "Orphanet:399", "Depressed nasal bridge {http": "HP:0005280", "Ly-76 high reticulocyte": "CL:0002019", "cytochalasin D": "CHEBI:529996", "hepatitis C virus induced hepatocellular carcinoma": "EFO:0008504", "infectious disease biomarker": "EFO:0006843", "egg allergy measurement": "EFO:0007018", "vancomycin": "CHEBI:28001", "Bartholin Gland Squamous Cell Carcinoma": "EFO:1000104", "hypopituitarism": "EFO:0001380", "CD38-positive IgG-negative class switched memory B cell": "CL:0002119", "large cell neuroendocrine carcinoma": "EFO:0000563", "GM17765 {http": "CLO:0016602", "embryonic stage 9": "EFO:0005869", "Epidermolysis bullosa simplex due to plakophilin deficiency": "Orphanet:158668", "clofibrate": "CHEBI:3750", "Childhood-onset hypophosphatasia": "Orphanet:247667", "Genetic syndromic Pierre Robin syndrome": "Orphanet:363294", "GM17108 {http": "CLO:0014889", "sphingomyelin": "CHEBI:17636", "Cholecystitis {http": "HP:0001082", "obstructive lung disease": "HP:0006536", "medullary breast carcinoma": "EFO:0000580", "labial sensory complex primordium": "FBbt:00005545", "Alar cartilages hypoplasia - coloboma - telecanthus": "Orphanet:2007", "Taurodontism": "Orphanet:3289", "leaf vascular tissue": "EFO:0001037", "cholesterol": "CHEBI:16113", "appendicular lean mass": "EFO:0004980", "eye measurement": "EFO:0004731", "continuous dark (no light) regimen": "EO:0007270", "chronic myelogenous leukemia cell line": "EFO:0005294", "3-(1H-indol-3-yl)propanoate {http": "CHEBI:82916", "chancre": "EFO:1001247", "BFTC-909": "EFO:0006538", "CS57886": "EFO:0000158", "DMS153": "EFO:0002163", "chemotherapy-induced alopecia": "EFO:0005400", "SK-N-SH": "EFO:0003072", "diastolic blood pressure change measurement": "EFO:0006945", "Rhodobacter sphaeroides 2.4.1": "NCBITaxon:272943", "Recurrent thrombophlebitis": "HP:0004419", "Bartter syndrome": "Orphanet:112", "ligament cell": "CL:0000384", "Polymicrogyria with optic nerve hypoplasia": "Orphanet:250972", "gliadin seropositivity": "EFO:0007049", "ALG11-CDG": "Orphanet:280071", "Familial hypoaldosteronism": "Orphanet:427", "Herpes Zoster": "EFO:0006510", "mouse neural progenitor cell": "EFO:0004039", "esophageal carcinoma": "EFO:0002916", "RNA-Seq": "EFO:0008896", "Brassica napus": "NCBITaxon:3708", "G22": "EFO:0006406", "scMT-Seq": "EFO:0008911", "succinate(1-) {http": "CHEBI:30779", "Lolium perenne": "NCBITaxon:4522", "spindle": "GO:0005819", "Brachycephaly {http": "HP:0000248", "GM10266": "EFO:0005335", "Trichorhinophalangeal syndrome type 1 and 3": "Orphanet:77258", "hidradenitis suppurativa": "EFO:1000710", "Pseudohypoaldosteronism type 2E": "Orphanet:300530", "Partial deletion of chromosome 12": "Orphanet:282124", "Citrullinemia": "Orphanet:187", "opportunistic Moraxellaceae infectious disease": "EFO:1001072", "Leuconostoc citreum": "NCBITaxon:33964", "Frasier syndrome": "Orphanet:347", "Collimonas fungivorans": "NCBITaxon:158899", "TCR-LA-MC PCR": "EFO:0008967", "Autosomal recessive spastic paraplegia type 75": "EFO:0009018", "Congenitally uncorrected transposition of the great arteries with cardiac malformation": "Orphanet:216729", "Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation": "Orphanet:300570", "Urinary incontinence": "HP:0000020", "triple-A syndrome": "EFO:1001997", "Mini-International Neuropsychiatric Interview": "EFO:0004786", "Focal palmoplantar keratoderma with joint keratoses": "Orphanet:370002", "transcriptomic data": "EFO:0004601", "GM17172 {http": "CLO:0014025", "CD34-positive, GlyA-negative erythroid progenitor cell": "CL:0002003", "Sylvia communis": "NCBITaxon:216193", "citrulline {http": "CHEBI:18211", "AL amyloidosis": "Orphanet:85443", "Formiminoglutamic aciduria": "Orphanet:51208", "Polar Spongioblastoma": "EFO:1000488", "Combined oxidative phosphorylation defect type 13": "Orphanet:319514", "Combined oxidative phosphorylation defect type 7": "Orphanet:254930", "Metarhizium": "NCBITaxon:5529", "Atrophy": "EFO:1000096", "endometrioid carcinoma": "EFO:0000466", "cell communication": "GO:0007154", "DKMG": "EFO:0002161", "Penicillium viridicatum": "NCBITaxon:60134", "Pasteurella multocida subsp. multocida str. Pm70": "NCBITaxon:272843", "Talipes equinovarus {http": "HP:0001762", "NOIR": "EFO:0008829", "muscular hypotonia {http": "HP:0001252", "platelet": "CL:0000233", "MEF cell line": "EFO:0004037", "Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type": "Orphanet:363444", "1,4-dichlorobenzene": "CHEBI:28618", "flag leaf {http": "PO:0020103", "immature CD11c-low plasmacytoid dendritic cell": "CL:0000992", "behavioral stimulus": "EFO:0000283", "Hereditary thrombophilia due to congenital protein C deficiency": "Orphanet:745", "marginal zone B cell": "CL:0000845", "Lateolabrax japonicus": "NCBITaxon:8164", "Cervical spina bifida cystica": "Orphanet:268762", "Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies": "Orphanet:397758", "Infantile hypophosphatasia": "Orphanet:247651", "Clostridia": "NCBITaxon:186801", "Osteoporosis - oculocutaneous hypopigmentation syndrome": "Orphanet:2786", "Inherited Creutzfeldt-Jakob disease": "Orphanet:282166", "GM20000": "EFO:0005352", "Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome": "EFO:0009050", "Anaplasma phagocytophilum": "NCBITaxon:948", "Progressive supranuclear palsy - progressive non fluent aphasia": "Orphanet:240112", "Appendix Neuroendocrine Tumor G1": "EFO:1000092", "occipital cortex": "UBERON:0016540", "Amish nemaline myopathy": "Orphanet:98902", "Illumina NovaSeq 6000": "EFO:0008637", "cantharidin": "CHEBI:64213", "Partial duplication of the long arm of chromosome 17": "Orphanet:262968", "Congenital muscular dystrophy type 1B": "Orphanet:98893", "Epithelioid Malignant Peripheral Nerve Sheath Tumor": "EFO:1000245", "Double outlet right ventricle with subpulmonary ventricular septal defect": "Orphanet:99045", "Opsismodysplasia": "Orphanet:2746", "external encapsulating structure part": "GO:0044462", "CEL-Seq": "EFO:0008679", "Pili torti - developmental delay - neurological abnormalities": "Orphanet:2891", "juxtacortical osteosarcoma": "EFO:1001000", "skin aging": "EFO:0005422", "African American": "EFO:0003150", "Choroideremia - deafness - obesity": "Orphanet:1435", "hindlimb muscle": "UBERON:0003663", "vagal placode 2": "UBERON:2001298", "colon mucinous adenocarcinoma": "EFO:0000364", "SUM44PE": "EFO:0001245", "theophylline": "CHEBI:28177", "immature NK T cell stage III": "CL:0002041", "Drosophila pseudoobscura bogotana": "NCBITaxon:46244", "GM17123 {http": "CLO:0015119", "blastula stage": "UBERON:0000108", "response to endocrine therapy": "EFO:0007613", "Dandy-Walker syndrome": "EFO:1000890", "MBDCap-Seq": "EFO:0008798", "disease progression measurement": "EFO:0008336", "Extramammary Paget Disease": "EFO:1000249", "Multiple metaphyseal dysplasia": "Orphanet:93430", "Cryptococcus gattii": "NCBITaxon:552467", "Ascending Colon Neuroendocrine Tumor G1": "EFO:1000094", "CD27-low, CD11b-low immature natural killer cell": "CL:0002345", "2102Ep": "EFO:0002957", "Physarum polycephalum": "NCBITaxon:5791", "Dihydropyrimidinuria": "Orphanet:38874", "Cataract associated with a metabolic disease": "Orphanet:98644", "intestinal necrosis": "EFO:0005632", "Disorder of bilirubin metabolism and excretion": "Orphanet:309816", "CME-W1-Cl.8+": "EFO:0005743", "N-methyl-D-aspartic acid": "CHEBI:31882", "stage II endometrioid carcinoma": "EFO:0000206", "androecium development stage {http": "PO:0007605", "BALB/cAnN": "EFO:0005286", "anastrozole": "CHEBI:2704", "Chronic hepatic porphyria": "Orphanet:95161", "PEO14": "EFO:0005446", "sepal {http": "PO:0009031", "isovalerate {http": "CHEBI:48942", "response to exercise": "EFO:0007768", "GM12873": "EFO:0001160", "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency": "Orphanet:88618", "Autosomal recessive spastic paraplegia type 20": "Orphanet:101000", "Tapered finger {http": "HP:0001182", "Ovarian Endometriosis": "EFO:1000418", "ferritin measurement": "EFO:0004459", "immature CD8_alpha-negative CD11b-negative dendritic cell": "CL:0001001", "follicle cell": "CL:0000477", "MEHMO syndrome": "Orphanet:85282", "glioblastoma H54": "EFO:0002782", "arthralgia": "HP:0002829", "La Crosse virus": "NCBITaxon:11577", "Congenital myopathy, Paradas type": "Orphanet:199329", "thrombin": "EFO:0003183", "astrocyte": "CL:0000127", "CS57836": "EFO:0000139", "Arabidopsis halleri": "NCBITaxon:81970", "chorea": "EFO:0004152", "scRNA-seq": "EFO:0008913", "FL-cDNA": "EFO:0003755", "Sf-2": "EFO:0006970", "susceptibility to plantar warts measurement": "EFO:0008406", "tooth ankylosis": "EFO:1001215", "NCI-H2722": "EFO:0006684", "Non hereditary congenital primary lymphedema": "Orphanet:79450", "Spondyloepiphyseal dysplasia, Kimberley type": "Orphanet:93283", "Triploidy": "Orphanet:3376", "PARIS": "EFO:0008847", "autoimmune thyroid disease": "EFO:0006812", "interleukin-6 measurement": "EFO:0004810", "IgG bisecting N-acetyl glucosamine measurement": "EFO:0008426", "REC1": "EFO:0002317", "Short stature - intellectual disability - eye anomalies - cleft lip/palate": "Orphanet:2649", "Spastic paraplegia - Paget disease of bone": "Orphanet:329475", "post-hyoid pharyngeal arch": "UBERON:0008896", "pulmonary sclerosing hemangioma": "EFO:1001136", "MURCS association": "Orphanet:2578", "N-acetyl-L-glutamate(1-) {http": "CHEBI:21549", "Bacillus anthracis str. Ames": "NCBITaxon:198094", "Bilateral frontoparietal polymicrogyria": "Orphanet:101070", "Phocomelia - ectrodactyly - deafness - sinus arrhythmia": "Orphanet:2878", "primary progressive multiple sclerosis": "EFO:0008520", "drug role": "EFO:0001899", "interleukin-14 (Mus musculus)": "EFO:0003799", "ischemia reperfusion injury": "EFO:0002687", "Xenopus (Silurana) tropicalis": "NCBITaxon:8364", "4-hydroxy-2-nonenal": "CHEBI:32585", "optic papillitis": "EFO:1001074", "MAGE-TAB array data matrix file": "EFO:0004097", "Giardia intestinalis": "NCBITaxon:5741", "acute hemorrhagic leukoencephalitis": "EFO:0007132", "papillary carcinoma": "EFO:1000646", "Frontonasal dysplasia": "Orphanet:250", "Combined deficiency of factor V and factor VIII": "Orphanet:35909", "Theiler stage 11": "EFO:0002582", "Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain": "Orphanet:324585", "Pyruvate dehydrogenase deficiency": "Orphanet:765", "Aspergillus versicolor": "NCBITaxon:46472", "callus formation": "GO:1990110", "Paralysis, Obstetric": "EFO:1001385", "Wistar-Kyoto": "EFO:0001345", "mood disorder": "EFO:0004247", "1-naphthyl isothiocyanate": "CHEBI:35455", "Helianthus annuus": "NCBITaxon:4232", "Oguchi disease": "Orphanet:75382", "Partial duplication of the short arm of chromosome 8": "Orphanet:262758", "KYSE-510": "EFO:0006631", "symmetrical dimethylarginine measurement": "EFO:0006523", "GM19240": "EFO:0002790", "angiomyoma": "EFO:1000806", "Von Willebrand disease type 1": "Orphanet:166078", "Metaphyseal dysostosis - intellectual disability - conductive deafness": "Orphanet:2502", "Theiler stage 24": "EFO:0002586", "Autosomal recessive lymphoproliferative disease": "Orphanet:238505", "Saccharomyces pastorianus": "NCBITaxon:27292", "Marfan syndrome": "Orphanet:558", "sensory bristle": "EFO:0000938", "prazosin": "CHEBI:8364", "CD34-negative, CD41-positive, CD42-positive megakaryocyte cell": "CL:0002026", "polar aprotic solvent role": "CHEBI:48358", "branchiostegal ray 2": "UBERON:2001281", "Spinal cord injury": "EFO:1001919", "GM17212 {http": "CLO:0013895", "Danaus plexippus": "NCBITaxon:13037", "anti-H3k4-3Me": "EFO:0005029", "anterior compartment syndrome": "EFO:1000808", "GM17188 {http": "CLO:0013777", "Adult familial nephronophthisis - spastic quadriparesia": "Orphanet:2666", "X-linked creatine transporter deficiency": "Orphanet:52503", "Bleeding diathesis due to glycoprotein VI deficiency": "Orphanet:98885", "CS57876": "EFO:0000155", "GTP cyclohydrolase I deficiency": "Orphanet:2102", "CS57626": "EFO:0000042", "KG1": "EFO:0002218", "IgE short lived plasma cell": "CL:0000951", "floral organ differentiation stage {http": "PO:0007600", "ejection fraction measurement": "EFO:0005527", "proplastid": "GO:0009537", "Syndactyly type 8": "Orphanet:2498", "chordotonal organ": "UBERON:0001038", "ureteral neoplasm": "EFO:0003844", "quality": "BFO:0000019", "low affinity immunoglobulin gamma Fc region receptor II-a/b measurement": "EFO:0008211", "Cholesteryl ester storage disease": "Orphanet:75234", "interleukin 17 measurement": "EFO:0008174", "diencephalon": "UBERON:0001894", "Wistar-Furth": "EFO:0001343", "Aarskog-Scott syndrome": "Orphanet:915", "miCLIP-m6A": "EFO:0008807", "mature T cell": "CL:0002419", "GM14452 {http": "CLO:0031263", "HPAC": "EFO:0002197", "Prader-Willi syndrome due to imprinting mutation": "Orphanet:177910", "tamoxifen": "CHEBI:41774", "ATC Code P Antiparasitic products, insecticides and repellents": "EFO:0005644", "prochlorperazine": "CHEBI:8435", "Genetic keratinization disorder associated with ocular features": "Orphanet:98697", "Warsaw breakage syndrome": "Orphanet:280558", "trophoblast cell": "CL:0000351", "Aphalangy - syndactyly - microcephaly": "Orphanet:1113", "osteopenia": "HP:0000938", "Partial deletion of the long arm of chromosome 21": "Orphanet:262173", "slow muscle cell somite 4": "ZFA:0000972", "inner cell mass": "UBERON:0000087", "3-methyladipic acid {http": "CHEBI:68503", "SCH": "EFO:0002856", "Rana pirica": "NCBITaxon:79017", "Uterine Inversion": "EFO:1001446", "Congenital Horner syndrome": "Orphanet:91413", "fully-elongated embryo Ce": "EFO:0005504", "Caldicellulosiruptor saccharolyticus": "NCBITaxon:44001", "scirrhous adenocarcinoma": "EFO:0007478", "late embryonic stage": "UBERON:0007220", "increased amount": "PATO:0000470", "Vitis aestivalis": "NCBITaxon:3605", "inosine-5'-monophosphate dehydrogenase 2 measurement": "EFO:0008159", "1-O-oleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:28610", "Aspergillus chevalieri": "NCBITaxon:182096", "ulna fracture": "EFO:0003950", "GM17287 {http": "CLO:0013082", "TERV": "EFO:0001249", "Cervical Clear Cell Adenocarcinoma": "EFO:1000163", "response to efavirenz": "EFO:0006904", "Ralstonia solanacearum UW551": "NCBITaxon:342110", "Deafness - genital anomalies - metacarpal and metatarsal synostosis": "Orphanet:3224", "Ferroglobus placidus": "NCBITaxon:54261", "Porphyria": "Orphanet:738", "Col-3": "EFO:0005151", "Drosophila virilis": "NCBITaxon:7244", "menadione sodium sulfonate": "CHEBI:63928", "Streptomyces microflavus": "NCBITaxon:1919", "Eiken syndrome": "Orphanet:79106", "anticoagulant": "CHEBI:50249", "high output heart failure": "EFO:0003145", "mole per liter": "EFO:0004381", "Humeral agenesis/hypoplasia, unilateral": "Orphanet:295061", "Campylobacter jejuni": "NCBITaxon:197", "Hypomaturation amelogenesis imperfecta": "Orphanet:100033", "Abnormality of the toenails": "HP:0008388", "B-cell acute lymphoblastic leukemia": "EFO:0000094", "Myopathy with hexagonally cross-linked tubular arrays": "Orphanet:171889", "inorganic chemical treatment {http": "EO:0001004", "N-acylethanolamine": "CHEBI:52640", "Malignant Mesothelioma": "EFO:1000355", "Penicillium fellutanum": "NCBITaxon:70095", "X-linked congenital generalized hypertrichosis": "Orphanet:79495", "CIRS-seq": "EFO:0008690", "cleavage 8-cell": "EFO:0001289", "RC-Seq": "EFO:0008885", "Leptospira interrogans": "NCBITaxon:173", "prostatitis": "EFO:0003830", "Late-onset junctional epidermolysis bullosa": "Orphanet:79406", "Brachydactyly of fingers, bilateral": "Orphanet:295130", "Autosomal dominant spastic paraplegia type 6": "Orphanet:100988", "Huntington disease-like 1": "Orphanet:157941", "SKI-DCLC": "EFO:0005460", "epidermis": "UBERON:0001003", "Cryptorchidism - arachnodactyly - intellectual disability": "Orphanet:1548", "(S)-3-phenyllactate {http": "CHEBI:32979", "dead": "PATO:0001422", "Leydig cell hypoplasia due to LHB deficiency": "Orphanet:325448", "parachordal vessel": "UBERON:2005034", "Festuca rubra subsp. fallax": "NCBITaxon:98754", "head mesoderm anlage": "FBbt:00005548", "ALG6-CDG": "Orphanet:79320", "Retroperitoneal Inflammatory Myofibroblastic Tumor": "EFO:1000510", "1-methyladenosine {http": "CHEBI:16020", "urogenital neoplasm": "EFO:0003863", "OVCAR5": "EFO:0005443", "pernicious anemia": "EFO:0005576", "jaw cancer": "EFO:0007333", "CC531": "EFO:0001101", "cognitive behavioural therapy": "EFO:0007820", "6-deoxocastasterone": "CHEBI:20712", "Job's syndrome": "EFO:0003775", "Macrothrombocytopenia with mitral valve insufficiency": "Orphanet:220448", "langerin-positive dermal dendritic cell": "CL:0002458", "Status Asthmaticus": "EFO:0008590", "GM17290 {http": "CLO:0013140", "Neurogenic arthrogryposis multiplex congenita": "Orphanet:1143", "gall tissue": "EFO:0000995", "Streptococcus gordonii": "NCBITaxon:1302", "alpha peak frequency measurement": "EFO:0006883", "Ursus americanus": "NCBITaxon:9643", "splenic tingible body macrophage": "CL:0000877", "chorea gravidarum": "EFO:1001290", "syphilis": "EFO:0007504", "CS57827": "EFO:0000135", "neuromuscular disease": "EFO:1001902", "mouth mucosa": "UBERON:0003729", "GM12248": "EFO:0001145", "Leprosy, Paucibacillary": "EFO:1001358", "Deafness - intellectual disability, Martin-Probst type": "Orphanet:85321", "14q22q23 microdeletion syndrome": "Orphanet:264200", "arsenic oxide": "CHEBI:50527", "Acrorenal syndrome": "Orphanet:971", "ventral wall of dorsal aorta": "UBERON:0018549", "melanoma cell line": "BTO:0000849", "Craniolenticulosutural dysplasia": "Orphanet:50814", "splenic disease": "EFO:0009002", "GP2d": "EFO:0006575", "Non-distal monosomy 10q": "Orphanet:1581", "immature dendritic epithelial T cell precursor": "CL:0002218", "embryonic day 12": "EFO:0007640", "Isolated distichiasis": "Orphanet:99177", "alcohol withdrawal delirium": "EFO:1000800", "Combined oxidative phosphorylation defect type 17": "Orphanet:369913", "response to high sodium diet": "EFO:0005401", "Sanfilippo syndrome type A": "Orphanet:79269", "Familial acute necrotizing encephalopathy": "Orphanet:88619", "interleukin 17 receptor B measurement": "EFO:0008176", "SKNFI": "EFO:0002338", "Orofaciodigital syndrome": "Orphanet:140997", "Familial partial lipodystrophy, Dunnigan type": "Orphanet:2348", "HPL1A": "EFO:0006907", "superior cervical ganglion": "UBERON:0001989", "adrenal gland hyperfunction": "EFO:1000797", "CD8_alpha-negative CD11b-negative dendritic cell": "CL:0000998", "aldosterone": "CHEBI:27584", "Populus deltoides": "NCBITaxon:3696", "Lissencephaly with cerebellar hypoplasia type C": "Orphanet:100013", "Enoplea infectious disease": "EFO:0007253", "Genital neoplasm, female": "EFO:1001331", "Dinoroseobacter shibae DFL 12": "NCBITaxon:398580", "Bosley-Salih-Alorainy syndrome": "Orphanet:69737", "fGS/OSS": "EFO:0005745", "ML-DmBG2-c2": "EFO:0005822", "Partial autosomal trisomy/tetrasomy": "Orphanet:98132", "3-hydroxylaurate {http": "CHEBI:76616", "prokaryotic cell": "CL:0000520", "DMS-MapSeq": "EFO:0008713", "Spastic ataxia": "Orphanet:316226", "lymphangioendothelioma": "EFO:1001026", "early promyelocyte": "CL:0002154", "ITM": "EFO:0002061", "2-oleoylglycerol {http": "CHEBI:73990", "Truncal dystonia": "Orphanet:93956", "Subaortic stenosis - short stature": "Orphanet:3191", "birth weight": "EFO:0004344", "mesenchymoma": "EFO:1001042", "Coronary Vasospasm": "EFO:0004225", "response to reward": "EFO:0008396", "Xanthomonas oryzae pv. oryzae KACC10331": "NCBITaxon:291331", "Senecio chrysanthemifolius": "NCBITaxon:121541", "abnormality of blood and blood-forming tissues": "HP:0001871", "GM17745 {http": "CLO:0016567", "dorsal closure stage": "FBdv:00005331", "BY4741": "EFO:0000098", "GM17242 {http": "CLO:0014412", "nonsyndromic deafness": "EFO:0009076", "spondylolysis": "EFO:0005649", "PAL-seq": "EFO:0008843", "CS57742": "EFO:0000083", "blood chromium measurement": "EFO:0007579", "Spondyloepimetaphyseal dysplasia, Handigodu type": "Orphanet:99642", "1-linoleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:28733", "GM17789 {http": "CLO:0016688", "encephalomalacia": "EFO:1000915", "stem internode": "PO:0020142", "Vagus Nerve Paraganglioma": "EFO:1000621", "homocitrate (-1) {http": "CHEBI:36459", "Agrobacterium larrymoorei": "NCBITaxon:160699", "leukocyte count": "EFO:0004308", "neuromyelitis optica": "EFO:0004256", "Multiple congenital anomalies-hypotonia-seizures syndrome type 2": "Orphanet:300496", "neuropathic pain": "EFO:0005762", "Orofaciodigital syndrome type 5": "Orphanet:2919", "Arabidopsis lyrata": "NCBITaxon:59689", "continuous light regimen {http": "EO:0007162", "Progressive distal Muscle weakness {http": "HP:0009063", "Sanfilippo syndrome type D": "Orphanet:79272", "Porphyromonas gingivalis ATCC 33277": "NCBITaxon:431947", "BCBL-1": "EFO:0002048", "serous cystadenoma": "EFO:0002504", "mediastinal lipomatosis": "EFO:1000732", "Familial hypercholanemia": "Orphanet:238475", "B10.NOD_H2g7": "EFO:0002739", "Familial sick sinus syndrome": "Orphanet:166282", "L1-S8R": "EFO:0007600", "Lactococcus lactis subsp. lactis Il1403": "NCBITaxon:272623", "Qualitative or quantitative defects of protein glycosyltransferase-like": "Orphanet:209027", "HepaRG": "EFO:0001186", "Coloboma of superior eyelid": "Orphanet:155884", "Hydatidiform Mole": "EFO:1000298", "Congenital hydronephrosis": "Orphanet:2190", "primordial germ cell": "CL:0000670", "Autosomal recessive hereditary demyelinating motor and sensory neuropathy": "Orphanet:140459", "Blepharophimosis {http": "HP:0000581", "inverted follicular keratosis": "EFO:1000717", "ITM-E6E7": "EFO:0002062", "GM15851": "EFO:0006277", "Congenital deficiency in alpha-fetoprotein": "Orphanet:168612", "Subcutaneous hemorrhage": "HP:0001933", "phyllid": "PO:0025075", "lead": "CHEBI:25016", "NPHP3-related Meckel-like syndrome": "Orphanet:3032", "P3HR1": "EFO:0002312", "1-naphthylacetic acid": "CHEBI:32918", "MDA-MB-330": "EFO:0006454", "melanoma staging": "EFO:0004954", "lung structure": "EFO:0001986", "Galactosemia": "Orphanet:352", "SQ-5": "EFO:0002861", "Felty's syndrome": "EFO:0007269", "BT549": "EFO:0001096", "Adrenal Gland Neuroblastoma": "EFO:1000075", "(R)-2-hydroxyoctadecanoate {http": "CHEBI:57562", "drought environment": "EO:0007404", "GM17148 {http": "CLO:0013940", "NCI-H292": "EFO:0006690", "vitamin": "CHEBI:33229", "white wine liking measurement": "EFO:0006948", "DamID": "EFO:0008704", "Senecio cambrensis": "NCBITaxon:285720", "TC-Seq": "EFO:0008964", "Multiple epiphyseal dysplasia, with miniepiphyses": "Orphanet:166032", "Persistent combined dystonia": "Orphanet:391711", "Non-syndromic limb malformation": "Orphanet:109011", "pimelate(1-) {http": "CHEBI:17774", "mid-arm muscle circumference measurement": "EFO:0008452", "Platichthys flesus": "NCBITaxon:8260", "Primary myoclonus": "Orphanet:306750", "Hereditary sensorimotor neuropathy with hyperelastic skin": "Orphanet:280598", "Methicillin-Resistant Staphylococcus Aureus Infection": "EFO:0008555", "proteomic profiling by mass spectrometer": "EFO:0002766", "chitosan": "CHEBI:16261", "Leukonychia totalis": "Orphanet:2387", "Fucosidosis": "Orphanet:349", "fluconazole": "CHEBI:46081", "ILSXISS14/TejJ": "EFO:0002975", "maxillary sinus cholesteatoma": "EFO:1000731", "dysentery": "EFO:1001869", "cyfluthrin": "CHEBI:4034", "L3055": "EFO:0001198", "leukocyte": "CL:0000738", "iPS-18b": "EFO:0007106", "HIV-Associated Lipodystrophy Syndrome": "EFO:1001348", "UCH-1": "EFO:0004389", "Gastrocutaneous syndrome": "Orphanet:2069", "Plasmodium falciparum antigen IgG3 measurement": "EFO:0007811", "immature NK T cell stage II": "CL:0002040", "primitive mesencephalic artery": "UBERON:2001062", "operator variation design": "EFO:0001772", "Citrus sinensis": "NCBITaxon:2711", "8p11.2 deletion syndrome": "Orphanet:251066", "Familial idiopathic dilatation of the right atrium": "Orphanet:1677", "3',5'-cyclic AMP": "CHEBI:17489", "Isolated congenital hypogonadotropic hypogonadism": "Orphanet:238666", "CCD-8Lu": "EFO:0005367", "midbrain basal plate": "UBERON:0010285", "Genetic epidermal disorder": "Orphanet:183426", "Juberg-Marsidi syndrome": "Orphanet:93972", "keto-phenylpyruvate {http": "CHEBI:18005", "Porokeratosis plantaris palmaris et disseminata": "Orphanet:737", "MPRA": "EFO:0008822", "Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia": "Orphanet:313808", "Pseudomonas fluorescens": "NCBITaxon:294", "sialolithiasis": "EFO:1001180", "Hypergonadotropic hypogonadism - cataract syndrome": "Orphanet:2410", "Vici syndrome": "Orphanet:1493", "Hernia": "HP:0100790", "isoxazole": "CHEBI:35595", "Biphasic Mesothelioma": "EFO:1000124", "folic acid": "CHEBI:27470", "Staphylococcus aureus subsp. aureus USA300": "NCBITaxon:367830", "Distal tetrasomy 15q": "Orphanet:314588", "Partial deletion of chromosome 3": "Orphanet:261776", "cortical collecting duct {http": "UBERON:0004203", "Color-vision disease": "Orphanet:98658", "Cortisol-Producing Adrenal Cortex Adenoma": "EFO:1000208", "Bayreuth ecotype": "EFO:0005174", "Genetic muscular channelopathy": "Orphanet:352298", "kidney neoplasm": "EFO:0003865", "GM15221 {http": "CLO:0027487", "COLO 679": "EFO:0006372", "response to erlotinib": "EFO:0007868", "SCLC-22H": "EFO:0006750", "blood cell (sensu Nematoda and Protostomia)": "CL:0000390", "O-[(4Z)-decenoyl]carnitine {http": "CHEBI:73048", "caudal fin {http": "UBERON:4000164", "nucleoside monophosphate biosynthetic process": "GO:0009124", "temperature": "EFO:0001702", "palatal neoplasm": "EFO:0003849", "Autosomal dominant medullary cystic kidney disease with hyperuricemia": "Orphanet:88950", "smoking cessation": "EFO:0004319", "non-narcotic analgesic": "CHEBI:35481", "OK-Seq": "EFO:0008837", "N(6)-acetyl-L-lysine {http": "CHEBI:17752", "brain vasculature": "UBERON:0005284", "week": "UO:0000034", "Athelia rolfsii": "NCBITaxon:39291", "Oxidative Stress": "EFO:1001905", "SNU-484": "EFO:0006755", "B220-low CD38-positive naive B cell": "CL:0002110", "X-linked lethal multiple pterygium syndrome": "Orphanet:79447", "Genetic nail anomaly": "Orphanet:183454", "Functional abnormality of the gastrointestinal tract": "HP:0012719", "thymic cortical macrophage": "CL:0000883", "dentary": "UBERON:0004742", "Synpolydactyly type 1": "Orphanet:295195", "Systemic Mastocytosis with Associated Clonal Hematological non-Mast-Cell Lineage Disease": "EFO:1000559", "sweat gland carcinoma": "EFO:0005591", "Nager syndrome": "Orphanet:245", "secondary lymphoid organ macrophage": "CL:0000867", "rate": "PATO:0000161", "NCI-H2195": "EFO:0002283", "Glycogen storage disease due to glycogenin deficiency": "Orphanet:263297", "blood vessel endothelial cell": "CL:0000071", "Alpha-thalassemia and related diseases": "Orphanet:275745", "16p13.11 microduplication syndrome": "Orphanet:261243", "Disorder of fucoglycosan synthesis": "Orphanet:309505", "Attenuated Ch\u00c3\u00a9diak-Higashi syndrome": "Orphanet:352723", "stomach endoderm": "EFO:0002580", "tetrabenazine": "CHEBI:9467", "Cleidorhizomelic syndrome": "Orphanet:1453", "Malignant Bone Neoplasm": "EFO:1000350", "Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma": "EFO:1000537", "constipation": "HP:0002019", "OCI-LY19": "EFO:0006709", "response to immunochemotherapy": "EFO:0007754", "Breast Diffuse Large B-Cell Lymphoma": "EFO:1000144", "NCI-H1651": "EFO:0002261", "Alpha-N-acetylgalactosaminidase deficiency type 2": "Orphanet:79280", "Malignant hyperthermia - arthrogryposis - torticollis": "Orphanet:2215", "Autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency": "Orphanet:352479", "postweaning multisystemic wasting syndrome": "EFO:1000048", "Familial cold urticaria": "Orphanet:47045", "chronic venous insufficiency": "EFO:0007940", "Persistent M\u00c3\u00bcllerian duct syndrome": "Orphanet:2856", "degree": "UO:0000185", "thromboangiitis obliterans": "EFO:1001211", "Death in infancy {http": "HP:0001522", "Zinc deficiency": "EFO:1000003", "VDJ-Seq": "EFO:0008981", "Treacher-Collins syndrome": "Orphanet:861", "NCI-H2810": "EFO:0006689", "TK-10": "EFO:0006765", "group assignment": "OBI:0600015", "metergoline": "CHEBI:64216", "abnormality of the immune system": "HP:0002715", "Disorder of folate metabolism and transport": "Orphanet:285657", "gamma-linoleic acid measurement": "EFO:0008363", "Cronobacter": "NCBITaxon:413496", "Ruminococcus flavefaciens": "NCBITaxon:1265", "Familial spontaneous pneumothorax": "Orphanet:2903", "cystatin-D measurement": "EFO:0008103", "cerebral arterial disease": "EFO:1000859", "flufenamic acid": "CHEBI:42638", "APOE carrier status": "EFO:0007659", "8p inverted duplication/deletion syndrome": "Orphanet:96092", "Rhizobium leguminosarum": "NCBITaxon:384", "Sterkiella histriomuscorum": "NCBITaxon:94289", "Coloboma of eye lens": "Orphanet:98943", "Autosomal recessive spondylometaphyseal dysplasia, M\u00c3\u00a9garban\u00c3\u00a9 type": "Orphanet:401979", "Thomas syndrome": "Orphanet:3316", "ankle brachial index": "EFO:0003912", "Corpus callosum agenesis - neuronopathy": "Orphanet:1496", "NCI-H1395": "EFO:0002252", "Gossypium arboreum": "NCBITaxon:29729", "infant grey matter volume measurement": "EFO:0008368", "Geospiza magnirostris": "NCBITaxon:48885", "Camurati-Engelmann disease": "Orphanet:1328", "attention deficit hyperactivity disorder": "EFO:0003888", "Barrett adenocarcinoma": "EFO:1001939", "Hereditary sensory and autonomic neuropathy type 6": "Orphanet:314381", "Glycogen storage disease due to phosphoglucomutase deficiency": "Orphanet:711", "Male infertility due to gonadal dysgenesis or sperm disorder": "Orphanet:399764", "insulinoma": "EFO:0000549", "KMS-21-BM": "EFO:0006614", "bulimia nervosa": "EFO:0005204", "7p22.1 microduplication syndrome": "Orphanet:314034", "teratocarcinoma-derived growth factor 1 measurement": "EFO:0008297", "Neonatal inflammatory skin and bowel disease": "Orphanet:294023", "hematopoietic lineage restricted progenitor cell": "CL:0002031", "GM17283 {http": "CLO:0013095", "response to disappointment": "EFO:0008397", "WNT1-inducible-signaling pathway protein 1 measurement": "EFO:0008321", "zygote": "CL:0000365", "Mandibulofacial dysostosis-microcephaly syndrome": "Orphanet:79113", "59M": "EFO:0006358", "Postaxial polydactyly of fingers": "Orphanet:294942", "BEAS-2B": "EFO:0001089", "Summitt syndrome": "Orphanet:3210", "nephrogenic fibrosing dermopathy": "EFO:1001814", "dental pulp exposure": "EFO:1001782", "blastoma": "EFO:0005785", "Autosomal recessive spastic paraplegia type 14": "Orphanet:100995", "nuclear lumen": "GO:0031981", "abscisic acid treatment {http": "EO:0007105", "tetrachloromethane": "CHEBI:27385", "seed maturation stage {http": "PO:0007632", "Rana chensinensis": "NCBITaxon:79015", "small intestine serosal dendritic cell": "CL:0002466", "intellectual disability - sparse hair - brachydactyly": "Orphanet:3051", "array specific design": "EFO:0004668", "M\u00c3\u00bcllerian aplasia": "Orphanet:73217", "Paenibacillus": "NCBITaxon:44249", "Antley-Bixler syndrome": "Orphanet:83", "Hyperphenylalaninemia": "Orphanet:238583", "embryonic corpus cardiacum": "EFO:0000449", "TT2 {http": "EFO:0005485", "endocrine system disease": "EFO:0001379", "ECC-1": "EFO:0005231", "B-cell non-Hodgkin lymphoma cell line": "EFO:0005906", "Paraplegia - intellectual disability - hyperkeratosis": "Orphanet:2824", "pre-B-I cell": "CL:0000956", "Cutaneous Follicular Lymphoma": "EFO:1000211", "Glossopalatine ankylosis": "Orphanet:141163", "gastric intestinal type adenocarcinoma": "EFO:0000504", "Autosomal dominant rhegmatogenous retinal detachment": "Orphanet:209867", "sick building syndrome": "EFO:0007484", "DroNc-Seq": "EFO:0008720", "Autosomal recessive cutis laxa type 2A": "Orphanet:357058", "Ureaplasma urealyticum urethritis": "EFO:1001225", "Autosomal recessive distal renal tubular acidosis": "Orphanet:402041", "basal plate": "UBERON:0004064", "Drosophila erecta": "NCBITaxon:7220", "Ovarian Sex Cord Tumor with Annular Tubules": "EFO:1000430", "specimen with known storage state": "OBI:0001472", "Autosomal recessive spastic paraplegia type 63": "Orphanet:401805", "S-allylcysteine {http": "CHEBI:74077", "dedifferentiated liposarcoma": "EFO:0003085", "Thyroid Gland Hyalinizing Trabecular Tumor": "EFO:1000588", "Pasteurella multocida": "NCBITaxon:747", "flatfoot": "EFO:0003874", "Leuconostoc pseudomesenteroides": "NCBITaxon:33968", "Familial long QT syndrome": "Orphanet:768", "noise-induced hearing loss": "EFO:1001254", "Pontocerebellar hypoplasia type 9": "Orphanet:369920", "Familial primary pulmonary hypoplasia": "Orphanet:2257", "tumor necrosis factor receptor II measurement": "EFO:0008384", "progesterone receptor status": "EFO:0005513", "Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency": "Orphanet:329249", "N-acetyl-D-methionine {http": "CHEBI:85210", "intermediate density lipoprotein measurement": "EFO:0008595", "human herpesvirus 6 seropositivity": "EFO:0007048", "non polyA RNA": "EFO:0005017", "Bardet-Biedl syndrome": "Orphanet:110", "Autosomal dominant brachyolmia": "Orphanet:93304", "lipid measurement": "EFO:0004529", "encephalitozoonosis": "EFO:0007250", "dropped head syndrome": "EFO:1001987", "Endometrial Squamous Cell Carcinoma": "EFO:1000240", "MDA": "EFO:0008800", "Distal trisomy 15q": "Orphanet:1707", "Anophthalmia/microphthalmia - esophageal atresia": "Orphanet:77298", "MCC-Seq": "EFO:0008799", "N2 lymph node stage": "EFO:0004934", "GM17258 {http": "CLO:0014394", "Primary Intraosseous Squamous Cell Carcinoma": "EFO:1000492", "Ovarian Gonadoblastoma": "EFO:1000420", "Intellectual disability - cataracts - calcified pinnae - myopathy": "Orphanet:3042", "Steatocystoma multiplex - natal teeth": "Orphanet:3184", "Genetic motor neuron disease": "Orphanet:98505", "ND01737 {http": "CLO:0016362", "Prominent nasal bridge {http": "HP:0000426", "white adipose tissue": "UBERON:0001347", "GM14382 {http": "CLO:0031198", "GM07055": "EFO:0001113", "cytoplasmic vesicle part": "GO:0044433", "20-hydroxyecdysone": "CHEBI:16587", "Photorhabdus luminescens subsp. laumondii TTO1": "NCBITaxon:243265", "Ig-Seq": "EFO:0008777", "Amelogenesis imperfecta and gingival hyperplasia syndrome": "Orphanet:171836", "Archaea": "NCBITaxon:2157", "tubular adenocarcinoma": "EFO:0006500", "Clostridium perfringens str. 13": "NCBITaxon:195102", "Kashin-Beck disease": "EFO:0006511", "Distal trisomy 10q": "Orphanet:96102", "blood metabolite measurement": "EFO:0005664", "Leukoencephalopathy - thalamus and brainstem anomalies - high lactate": "Orphanet:314051", "MBD-seq": "EFO:0003750", "Ectodermal dysplasia - cutaneous syndactyly syndrome": "Orphanet:247827", "Nephrogenic syndrome of inappropriate antidiuresis": "Orphanet:93606", "transport": "GO:0006810", "monopoietic cell": "CL:0002194", "inflammatory biomarker measurement": "EFO:0004872", "Arbovirus Infections": "EFO:1001269", "cohort": "EFO:0004445", "abacavir": "CHEBI:2360", "Serotonin Syndrome": "EFO:1001842", "AG04351 {http": "CLO:0034796", "Small Intestinal Intraepithelial Neoplasia": "EFO:1000536", "persian gulf syndrome": "EFO:0007430", "head circumference": "EFO:0005114", "Brachyolmia type 1, Hobaek type": "Orphanet:93301", "Leber hereditary optic neuropathy": "Orphanet:104", "Salmonella enterica subsp. enterica serovar Emek": "NCBITaxon:286784", "diet": "EFO:0002755", "GM12003": "EFO:0001128", "HIV viral set point measurement": "EFO:0006319", "traumatic diaphragmatic hernia": "EFO:1001861", "Leydig cell hypoplasia": "Orphanet:755", "Constitutional megaloblastic anemia due to folate metabolism disorder": "Orphanet:98408", "fetal genotype effect measurement": "EFO:0007959", "EH": "EFO:0007748", "array scanner": "OBI:0400104", "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation": "Orphanet:300751", "Potocki-Shaffer syndrome": "Orphanet:52022", "PB-seq": "EFO:0008854", "articular cartilage of joint {http": "UBERON:0010996", "Duplex-Seq": "EFO:0008727", "passage number": "EFO:0007061", "Adrenal Hyperandrogenism": "EFO:0009007", "orchitis": "EFO:1001078", "Tay-Sachs disease, B variant, infantile form": "Orphanet:309178", "hair shape measurement": "EFO:0007824", "nucleoside monophosphate metabolic process": "GO:0009123", "Helicos sequencing": "OBI:0000697", "Miyoshi myopathy": "Orphanet:45448", "knee joint": "UBERON:0001485", "Early-onset progressive neurodegeneration - blindness - ataxia - spasticity": "Orphanet:352654", "L428": "EFO:0002225", "Tay-Sachs disease, B variant, adult form": "Orphanet:309192", "(S)-malate(2\u00e2\u0088\u0092) {http": "CHEBI:15589", "folate deficiency": "EFO:0001070", "Xeroderma pigmentosum complementation group B": "Orphanet:276252", "axial vasculature": "UBERON:2001073", "blood vessel": "UBERON:0001981", "speech perception": "EFO:0004336", "flower bud {http": "PO:0000056", "Genetic syndrome with a Dandy-Walker malformation as major feature": "Orphanet:269570", "Cavernous Hemangioma of the Face": "EFO:1000152", "vasoconstrictor agent": "CHEBI:50514", "Marchiafava-Bignami Disease": "EFO:1001809", "myeloid dendritic cell": "CL:0000782", "acute hemorrhagic conjunctivitis": "EFO:0007131", "X-linked intellectual disability, Stocco Dos Santos type": "Orphanet:85288", "nuc-ChIP-seq": "EFO:0008833", "Lissencephaly with cerebellar hypoplasia type E": "Orphanet:100015", "mixed connective tissue disease": "EFO:0007374", "Pfeiffer": "EFO:0006472", "Rectal Tubulovillous Adenoma": "EFO:1000505", "fC-Seal": "EFO:0008740", "Congenital disorder of glycosylation with neurological involvement": "Orphanet:371047", "N-acetyl-L-cysteine": "CHEBI:28939", "Autosomal recessive leukoencephalopathy with ischemic stroke-retinitis pigmentosa syndrome": "Orphanet:314572", "hair color": "EFO:0003924", "intracerebral hemorrhage": "EFO:0005669", "Chudley-Lowry-Hoar syndrome": "Orphanet:93971", "Japanese": "EFO:0003164", "osteoporosis": "EFO:0003882", "primary angle closure glaucoma": "EFO:1001506", "ATC Code H Systemic hormonal preparations, excluding sex hormones and insulins": "EFO:0005639", "photosynthetic cell": "CL:0000628", "(+)-dexrazoxane": "CHEBI:50223", "Streptococcus oralis": "NCBITaxon:1303", "Koolen-De Vries syndrome due to a point mutation": "Orphanet:363965", "Familial adenomatous polyposis due to 5q22.2 microdeletion": "Orphanet:261584", "type I NK T cell": "CL:0000921", "Euphorbia esula": "NCBITaxon:3993", "Atypical Endometrial Hyperplasia": "EFO:1000098", "pneumonia": "EFO:0003106", "Nematoda {http": "EO:0007337", "Distal monosomy 13q": "Orphanet:1590", "Machado-Joseph disease type 1": "Orphanet:276238", "iPS-11c": "EFO:0007101", "caudal vein plexus": "UBERON:2001286", "Organic aciduria": "Orphanet:289899", "thyroxine measurement": "EFO:0005130", "Tessier number 5 facial cleft": "Orphanet:141261", "Gossypium mustelinum": "NCBITaxon:34275", "Congenital stationary night blindness": "Orphanet:215", "immature NK T cell stage I": "CL:0002039", "Asian/Pacific Islander": "EFO:0003154", "Sickle cell disease and related diseases": "Orphanet:275752", "SU-DHL-8": "EFO:0006493", "Mycoplasma hyopneumoniae": "NCBITaxon:2099", "CS57715": "EFO:0000071", "abscisic acid": "CHEBI:22152", "suppurative otitis media": "EFO:0007503", "stem elongation stage {http": "PO:0007089", "H1-hESC": "EFO:0003042", "Congenitally uncorrected transposition of the great arteries with coarctation": "Orphanet:99042", "tuberculoid leprosy": "EFO:0001056", "adult midgut precursor": "EFO:0000244", "Spondyloepimetaphyseal dysplasia, aggrecan type": "Orphanet:171866", "Clostridium perfringens": "NCBITaxon:1502", "Tribolium castaneum": "NCBITaxon:7070", "GM17805 {http": "CLO:0016498", "Brain Stem Glioblastoma": "EFO:1000141", "GM17274 {http": "CLO:0013193", "coagulation factor V measurement": "EFO:0008087", "SUDHL6": "EFO:0002357", "alpha-tocopherol": "CHEBI:22470", "Spondyloepimetaphyseal dysplasia, Shohat type": "Orphanet:93352", "Lactobacillus plantarum WCFS1": "NCBITaxon:220668", "CAST-ChIP": "EFO:0008676", "Hyponatremia": "HP:0002902", "Primary lateral sclerosis": "Orphanet:35689", "morphologic finding": "EFO:0008513", "KP-3": "EFO:0006622", "KLM-1": "EFO:0006610", "adult muscle precursor primordium": "FBbt:00005516", "erythema infectiosum": "EFO:1000693", "X-linked complex spastic paraplegia": "Orphanet:98888", "Immunodeficiency with natural-killer cell deficiency and adrenal insufficiency": "Orphanet:75391", "dirofilariasis": "EFO:0007239", "Lissencephaly type 3": "Orphanet:102011", "Lipoma associated with neurospinal dysraphism": "Orphanet:268832", "non-classical monocyte": "CL:0000875", "Achondrogenesis type 1A": "Orphanet:93299", "Hippoglossus hippoglossus": "NCBITaxon:8267", "Syndromic aniridia": "Orphanet:98557", "Ectodermal dysplasia - sensorineural deafness": "Orphanet:1883", "alcoholic pancreatitis": "EFO:1002013", "carbohydrate derivative biosynthetic process": "GO:1901137", "ML-DmD16-c3": "EFO:0005825", "bark": "PO:0004518", "GM17284 {http": "CLO:0013092", "Coloboma of eyelid": "Orphanet:98946", "Complex Cyst of Kidney": "EFO:0008616", "hepatic methionine adenosyltransferase deficiency": "EFO:0009069", "DBTRG05MG": "EFO:0002159", "ST88-14": "EFO:0006295", "Rare genetic immune disease": "Orphanet:183770", "plasma trimethylamine N-oxide measurement": "EFO:0005691", "homovanillate (HVA) {http": "CHEBI:545959", "GM14501 {http": "CLO:0031504", "Amphimedon queenslandica": "NCBITaxon:400682", "Ajellomyces capsulatus": "NCBITaxon:5037", "Euphorbia pulcherrima": "NCBITaxon:37495", "Dermato-cardio-skeletal syndrome, Borrone type": "Orphanet:1266", "G120": "EFO:0006398", "round cell liposarcoma": "EFO:0003084", "Aniridia - cerebellar ataxia - intellectual disability": "Orphanet:1065", "WGA-X": "EFO:0008984", "MDAMB436": "EFO:0001214", "MIN6": "EFO:0002829", "Nijmegen breakage syndrome": "Orphanet:647", "Oenococcus oeni": "NCBITaxon:1247", "PENS syndrome": "Orphanet:313936", "Shigella flexneri 2a str. 301": "NCBITaxon:198214", "Low phospholipid associated cholelithiasis": "Orphanet:69663", "Autosomal uniparental disomy": "Orphanet:98152", "nucleoside biosynthetic process": "GO:0009163", "NCI-H596": "EFO:0006694", "Mosaic trisomy 5": "Orphanet:96060", "NCI-H226": "EFO:0002285", "Daphnia pulicaria": "NCBITaxon:35523", "Shigella flexneri": "NCBITaxon:623", "10q22.3q23.3 microduplication syndrome": "Orphanet:276422", "benzoic acid": "CHEBI:30746", "Syndactyly type 3": "Orphanet:93404", "somatic muscle primordium": "FBbt:00005518", "serum amyloid P-component measurement": "EFO:0008283", "knee peak torque measurement": "EFO:0007854", "A2780": "EFO:0006362", "Metabolic disease with dementia": "Orphanet:98543", "scrub typhus": "EFO:0007480", "SW948": "EFO:0002375", "PLB985": "EFO:0002313", "diffuse intrinsic pontine glioma": "EFO:1000026", "Klinefelter's syndrome": "EFO:1001006", "coffee consumption measurement": "EFO:0006781", "Epispadias": "Orphanet:93928", "urgency urinary incontinence": "EFO:0006865", "Falco chicquera": "NCBITaxon:495941", "alcoholic liver disease": "EFO:0008573", "GM12878": "EFO:0002784", "X-linked intellectual disability, Pai type": "Orphanet:85322", "lichen nitidus": "EFO:1000725", "renal cell carcinoma cell line": "BTO:0000383", "Hereditary persistence of alpha-fetoprotein": "Orphanet:168615", "severe global developmental delay {http": "HP:0011344", "vagal ganglion 1": "UBERON:2001302", "submitted": "EFO:0001794", "GM17850 {http": "CLO:0016450", "Deaf blind hypopigmentation syndrome, Yemenite type": "Orphanet:3214", "Limanda limanda": "NCBITaxon:27771", "Syndromic X-linked intellectual disability due to JARID1C mutation": "Orphanet:85279", "BMI-adjusted hip circumference": "EFO:0008039", "extraversion measurement": "EFO:0007913", "enrichment of methylated DNA": "EFO:0004185", "biosynthetic process": "GO:0009058", "Hereditary hypercarotenemia and vitamin A deficiency": "Orphanet:199285", "Intermediate osteopetrosis": "Orphanet:210110", "isoprenoid": "CHEBI:24913", "chemokine (C-C motif) ligand 27 measurement": "EFO:0008082", "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency": "Orphanet:319574", "helping behaviour": "EFO:0008540", "creatinine clearance measurement": "EFO:0007934", "Partial trisomy of the long arm of chromosome 9": "Orphanet:262905", "Ampulla of Vater Carcinoma": "EFO:1000079", "illness severity status": "EFO:0007863", "Prominent glabella - microcephaly - hypogenitalism": "Orphanet:2083", "carcinoid tumor": "EFO:0004243", "Arthrogryposis multiplex congenita - whistling face": "Orphanet:1150", "Pierre Robin syndrome associated with collagen disease": "Orphanet:138041", "physical activity measurement": "EFO:0008002", "geniculate ganglion": "UBERON:0001700", "Listeria monocytogenes 10403S": "NCBITaxon:393133", "SNU423": "EFO:0002348", "stylopod": "UBERON:0002472", "Autosomal recessive spondylocostal dysostosis": "Orphanet:2311", "cranial division of the internal carotid artery": "UBERON:2001059", "Aniridia - renal agenesis - psychomotor retardation": "Orphanet:1064", "population": "OBI:0000181", "Semilobar holoprosencephaly": "Orphanet:220386", "12,13-DiHOME {http": "CHEBI:72665", "Microcornea-myopic chorioretinal atrophy-telecanthus syndrome": "Orphanet:369970", "commensal Clostridium infectious disease": "EFO:1000874", "CD38-positive IgG memory B cell": "CL:0002105", "Subepithelial mucinous corneal dystrophy": "Orphanet:98959", "SHORT syndrome": "Orphanet:3163", "ecotype": "EFO:0000434", "Hypophosphatemic rickets": "Orphanet:437", "Cholecystitis, Acute": "EFO:1001289", "mosquito bite reaction size measurement": "EFO:0008378", "disturbed flow regions": "EFO:0002750", "membrane raft": "GO:0045121", "Mediastinal Cyst": "EFO:1001368", "Macrosomia - microphthalmia - cleft palate": "Orphanet:2432", "ME-1": "EFO:0006645", "Major Salivary Gland Carcinoma": "EFO:1000344", "AKR/J": "EFO:0007726", "magnesium dichloride": "CHEBI:6636", "Rare hyperlipidemia": "Orphanet:181422", "3H-1,2-dithiole-3-thione": "CHEBI:50866", "Hypercalcemia": "HP:0003072", "retina": "UBERON:0000966", "Mandibulofacial dysostosis - macroblepharon - macrostomia": "Orphanet:357158", "homocysteine measurement": "EFO:0004578", "Autosomal dominant epilepsy with auditory features": "Orphanet:101046", "bisphenol A": "CHEBI:33216", "Maternally-inherited mitochondrial myopathy": "Orphanet:254788", "CS57655": "EFO:0000053", "trimethylamine N-oxide {http": "CHEBI:15724", "Ceratitis capitata": "NCBITaxon:7213", "Placental Choriocarcinoma": "EFO:1000479", "arsenite(3-)": "CHEBI:29866", "Arachis hypogaea": "NCBITaxon:3818", "CD69-positive, CD8-positive single-positive thymocyte": "CL:0002435", "G4-seq": "EFO:0008751", "Fusarium equiseti": "NCBITaxon:61235", "trichomoniasis": "DOID:1947", "C0202": "EFO:0007072", "Tourette syndrome": "EFO:0004895", "Hartnup disease": "Orphanet:2116", "Lentinula edodes": "NCBITaxon:5353", "Short rib-polydactyly syndrome, Majewski type": "Orphanet:93269", "GM17831 {http": "CLO:0016522", "fibronectin fragment 4 measurement": "EFO:0008132", "malignant rhabdoid tumour": "EFO:0005701", "46,XY disorder of gonadal development": "Orphanet:325118", "GM17232 {http": "CLO:0014344", "oenocyte primordium": "FBbt:00017020", "VACTERL/VATER association": "Orphanet:887", "central brain primordium": "FBbt:00005542", "Ludwig's angina": "EFO:1000730", "Kidney Oncocytoma": "EFO:1000315", "Bone Epithelioid Hemangioma": "EFO:1000132", "N-acetyl-beta-alanine {http": "CHEBI:16682", "GM17799 {http": "CLO:0016490", "umbilical cord": "UBERON:0002331", "B6.H2_g7": "EFO:0002742", "Macrotia {http": "HP:0000400", "cerebral blood flow measurement": "EFO:0007980", "Parasteatoda tepidariorum": "NCBITaxon:114398", "loxtidine": "CHEBI:6550", "sporotrichosis": "EFO:0007494", "Lichstenstein syndrome": "Orphanet:2390", "X-linked intellectual disability - cerebellar hypoplasia": "Orphanet:137831", "Combined hyperlipidemia": "Orphanet:79211", "gene knock in": "EFO:0004963", "Double outlet right ventricle": "Orphanet:3426", "postprandial hyperlipidemia": "EFO:0007632", "GM17267 {http": "CLO:0013179", "staurosporine": "CHEBI:15738", "Heterotaxia": "EFO:0009081", "Postaxial polydactyly type A, bilateral": "Orphanet:295165", "Lycopersicon": "NCBITaxon:49274", "dorsal metathoracic disc": "UBERON:6001779", "NCI-H2198": "EFO:0006677", "Cenchrus americanus": "NCBITaxon:4543", "type 2 diabetes nephropathy": "EFO:0004997", "Drosophila mojavensis": "NCBITaxon:7230", "arabinonate {http": "CHEBI:22595", "trans fatty acid measurement": "EFO:0006821", "NCI-H196": "EFO:0006668", "Parietal foramina": "Orphanet:60015", "Laminopathy type Decaudain-Vigouroux": "Orphanet:137871", "response to mineral dust exposure": "EFO:0006993", "Methylmalonic acidemia with homocystinuria, type cblJ": "Orphanet:369955", "embryonic stage 8": "EFO:0005868", "Rare male infertility due to testicular endocrine disorder": "Orphanet:399685", "46,XY disorder of sex development due to testosterone synthesis defect": "Orphanet:90783", "spatial transcriptomics": "EFO:0008994", "Autosomal dominant slowed nerve conduction velocity": "Orphanet:140481", "Dysautonomia": "HP:0002459", "Propionibacterium acnes": "NCBITaxon:1747", "antimicrobial agent": "CHEBI:33281", "Pontocerebellar hypoplasia type 5": "Orphanet:166068", "capillary": "UBERON:0001982", "Autosomal recessive syndromic optic atrophy": "Orphanet:98677", "Mitochondrial disease with hypertrophic cardiomyopathy": "Orphanet:217587", "alpha-linolenic acid measurement": "EFO:0007759", "tocopherol measurement": "EFO:0004738", "Hemoglobin C disease": "Orphanet:2132", "Bos taurus": "NCBITaxon:9913", "Fischer 344": "EFO:0000176", "alveolar bone": "BTO:0001383", "Lateral meningocele syndrome": "Orphanet:2789", "meter": "UO:0000008", "antiphospholipid syndrome": "EFO:0002689", "Lowry-Wood syndrome": "Orphanet:1824", "cerebral small vessel disease": "EFO:0008493", "Lactobacillus curvatus": "NCBITaxon:28038", "purine nucleotide biosynthetic process": "GO:0006164", "brain hypoxia": "EFO:1001766", "viability": "PATO:0000169", "Duodenal Gastrin-Producing Neuroendocrine Tumor": "EFO:1000224", "ceftriaxone": "CHEBI:29007", "GM17272 {http": "CLO:0013214", "GM17768 {http": "CLO:0016597", "HIV-1 infection": "EFO:0000180", "estrone conjugate measurement": "EFO:0007971", "Autosomal recessive spastic paraplegia type 24": "Orphanet:101004", "FRT-Seq": "EFO:0008748", "antioxidant": "CHEBI:22586", "size": "EFO:0001695", "Citrullinemia type I": "Orphanet:247525", "(9R,13R)-12-oxo-phytodienoic acid": "CHEBI:34005", "Pseudonocardia dioxanivorans": "NCBITaxon:240495", "H0287": "EFO:0002776", "Spinocerebellar ataxia type 13": "Orphanet:98768", "generalised epilepsy": "EFO:0005917", "N-methylproline {http": "CHEBI:90344", "Coronary Restenosis": "EFO:0004224", "A431": "EFO:0006268", "Hereditary sensory and autonomic neuropathy": "Orphanet:140471", "Triticum mosaic virus {http": "NCBITaxon:431317", "reflex epilepsy": "EFO:1001146", "Congenital neuronal ceroid lipofuscinosis": "Orphanet:168486", "properdin measurement": "EFO:0008269", "reactive cutaneous fibrous lesion": "EFO:1000759", "risk status": "EFO:0000686", "ciprofibrate": "CHEBI:50867", "pneumatosis cystoides intestinalis": "EFO:1001113", "46,XY disorder of sex development of gynecological interest": "Orphanet:325632", "Mitochondrial disease with peripheral neuropathy": "Orphanet:225703", "GM11881": "EFO:0001122", "GM17209 {http": "CLO:0013875", "thymus neoplasm": "EFO:0002626", "Cystoid macular dystrophy": "Orphanet:75381", "Butyrylcholinesterase deficiency": "Orphanet:132", "KARPAS 1106P": "EFO:0006606", "thoracic aortic aneurysm": "EFO:0004282", "Carnitine palmitoyl transferase II deficiency, neonatal form": "Orphanet:228308", "Rare genetic skin disease": "Orphanet:68346", "diaphragmatic hernia": "EFO:0008561", "bladder calculus": "EFO:1000839", "Isotretinoin-like syndrome": "Orphanet:2306", "indoxyl sulfate {http": "CHEBI:43355", "GM17293 {http": "CLO:0013137", "aggressive insulitis": "EFO:0002498", "acalculous cholecystitis": "EFO:1000790", "intraepithelial lymphocyte": "CL:0002496", "infertility": "EFO:0000545", "Limb transversal defect - cardiac anomaly": "Orphanet:2492", "Streptomyces venezuelae": "NCBITaxon:54571", "Upper limb hypertrophy": "Orphanet:295049", "HT1376": "EFO:0002203", "tissue factor pathway inhibitor measurement": "EFO:0007968", "pleural tuberculosis": "EFO:0007446", "genital herpes": "EFO:0007282", "blastocyst": "UBERON:0000358", "Primary dystonia, DYT4 type": "Orphanet:98805", "YMB-1": "EFO:0006779", "Central precocious puberty": "EFO:0009029", "fludrocortisone": "CHEBI:50885", "SERKAL syndrome": "Orphanet:139466", "Early-onset autosomal dominant Alzheimer disease": "Orphanet:1020", "Parathyroid Gland Carcinoma": "EFO:1000456", "CD27-negative gamma-delta T cell": "CL:0002125", "Severe combined immunodeficiency due to CARD11 deficiency": "Orphanet:357237", "coagulation factor measurement": "EFO:0004634", "dracunculiasis": "EFO:0007241", "apomorphine hydrochloride": "CHEBI:31228", "acute erythroblastic leukemia": "EFO:1001257", "Thermoproteus tenax": "NCBITaxon:2271", "CD8alpha-positive thymic conventional dendritic cell": "CL:0002059", "Postthrombotic Syndrome": "EFO:1001405", "infection": "EFO:0000544", "Neonatal insulin-dependent diabetes mellitus {http": "HP:0000857", "Hydrolethalus": "Orphanet:2189", "Atelosteogenesis type II": "Orphanet:56304", "data set": "IAO:0000100", "bladder transitional cell carcinoma": "EFO:0006544", "specimen vial": "EFO:0005535", "postmenopausal osteoporosis": "EFO:0003854", "Bordetella holmesii": "NCBITaxon:35814", "Theiler stage 16": "EFO:0004407", "myeloperoxidase measurement": "EFO:0005243", "CS57924": "EFO:0000166", "neuromast": "UBERON:0008904", "splenic metallophillic macrophage": "CL:0000873", "Lotus corniculatus": "NCBITaxon:47247", "Ovarian Stromal Luteoma": "EFO:1000434", "Inflammation of the large intestine": "HP:0002037", "sleep quality": "EFO:0005272", "Severe combined immunodeficiency due to complete RAG1/2 deficiency": "Orphanet:331206", "Anas platyrhynchos": "NCBITaxon:8839", "Adrenal Gland Myelolipoma": "EFO:1000074", "apoptotic process": "GO:0006915", "FACS-seq": "EFO:0008735", "sodium cholate": "CHEBI:26711", "Blau syndrome": "Orphanet:90340", "Arthroderma otae": "NCBITaxon:63405", "Anonychia - onychodystrophy": "Orphanet:90390", "microglial cell": "CL:0000129", "Saccharomyces mikatae": "NCBITaxon:114525", "Xeroderma pigmentosum complementation group G": "Orphanet:276267", "Hurler-Scheie syndrome": "Orphanet:93476", "sensory neuron": "CL:0000101", "Primary immunodeficiency syndrome due to p14 deficiency": "Orphanet:90023", "Atypical hemolytic-uremic syndrome with B factor anomaly": "Orphanet:93578", "Antenatal Bartter syndrome": "Orphanet:93604", "neurodegeneration": "HP:0002180", "Myosclerosis": "Orphanet:289380", "cigarettes per day measurement": "EFO:0006525", "X-linked pure spastic paraplegia": "Orphanet:320332", "Oculootodental syndrome": "Orphanet:99806", "Juvenile glaucoma": "Orphanet:98977", "cholate {http": "CHEBI:29747", "ClickSeq": "EFO:0008694", "external encapsulating structure": "GO:0030312", "AN3CA": "EFO:0002110", "acute chest syndrome": "EFO:0007129", "Ct-1": "EFO:0006982", "Moebius syndrome": "Orphanet:570", "tumor necrosis factor beta measurement": "EFO:0008308", "Thermotoga petrophila": "NCBITaxon:93929", "plasma cell": "CL:0000786", "GM17840 {http": "CLO:0016524", "ES-I3": "EFO:0007076", "celastrol": "CHEBI:63959", "Chrysolophus pictus": "NCBITaxon:9089", "oligomycin": "CHEBI:25675", "AACOCF3": "CHEBI:2341", "Histophilus somni": "NCBITaxon:731", "Bromus inermis": "NCBITaxon:15371", "2-oleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:76071", "Staphylococcus lentus": "NCBITaxon:42858", "Trimethylaminuria {http": "HP:0003614", "uniconazole-P": "CHEBI:38000", "Microcornea - glaucoma - absent frontal sinuses": "Orphanet:2536", "cilium": "GO:0005929", "female genital tract polyp": "EFO:0008622", "Familial hyperthyroidism due to mutations in TSH receptor": "Orphanet:424", "SNU-719": "EFO:0006760", "shoot apical meristem": "PO:0020148", "Hypoplasia of the frontal lobes {http": "HP:0007333", "t-tau measurement": "EFO:0004760", "polyA RNA": "OBI:0000869", "Autosomal recessive degenerative and progressive cerebellar ataxia": "Orphanet:98098", "1182-4H": "EFO:0005648", "Superficial epidermolytic ichthyosis": "Orphanet:455", "Anolis carolinensis": "NCBITaxon:28377", "Ichthyosis hystrix of Curth-Macklin": "Orphanet:79503", "DV-90": "EFO:0006565", "Burkholderia multivorans": "NCBITaxon:87883", "caffeic acid 3-sulfate {http": "CHEBI:90242", "Thrombophlebitis": "HP:0004418", "Desulfovibrio alaskensis G20": "NCBITaxon:207559", "apocrine sweat gland": "UBERON:0000382", "Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation": "Orphanet:93214", "Biomphalaria glabrata": "NCBITaxon:6526", "parathyroid adenoma": "EFO:1001087", "brassinolide": "CHEBI:28277", "body composition measurement": "EFO:0005106", "Autosomal dominant striatal neurodegeneration": "Orphanet:228169", "pancreatic ductal adenocarcinoma": "EFO:0002517", "Distal lower limb Muscle weakness {http": "HP:0009053", "CD94-negative, Ly49CI-negative natural killer cell": "CL:0002442", "neural keel": "UBERON:0007135", "Biotin-responsive basal ganglia disease": "Orphanet:65284", "bone of lower extremity": "UBERON:0003464", "opisthorchiasis": "EFO:0007404", "vertebra": "UBERON:0002412", "Thermus thermophilus HB8": "NCBITaxon:300852", "CS57569": "EFO:0000017", "Heat Stroke": "EFO:1001340", "Otopalatodigital syndrome type 1": "Orphanet:90650", "latissimus dorsi": "EFO:0003067", "N231": "EFO:0002840", "intestine": "UBERON:0000160", "DArTSeq": "EFO:0008706", "array control empty": "EFO:0005435", "Theiler stage 5": "EFO:0004397", "S-sulfo-L-cysteine {http": "CHEBI:27891", "Gossypium darwinii": "NCBITaxon:34276", "oligodendroglioma": "EFO:0000632", "OVCA420": "EFO:0006720", "Thalassemia": "EFO:1001996", "response to cold pressor test": "EFO:0005404", "46,XX gonadal dysgenesis": "Orphanet:243", "dichloroacetate": "CHEBI:28240", "secondary hypertension": "EFO:1002034", "Netherton syndrome": "Orphanet:634", "vaccination": "EFO:0004292", "epitheloid cell": "CL:0002150", "presumptive rhombomere 4": "UBERON:0007291", "Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency": "Orphanet:217467", "Disorder of glycolysis": "Orphanet:308459", "anaplastic astrocytoma": "EFO:0002499", "stem cell derived cell line": "EFO:0002886", "retinal artery occlusion": "EFO:1001154", "T87": "EFO:0006305", "malignant epitheloid mesothelioma": "EFO:1000351", "CB184": "EFO:0004047", "RBBS": "EFO:0008883", "familial amyloid neuropathy": "EFO:0004129", "hypothyroidism": "EFO:0004705", "Benign Ovarian Neoplasm": "EFO:1000116", "Immunodeficiency syndrome with autoimmunity": "Orphanet:169355", "Theiler stage 7": "EFO:0004399", "milk allergic reaction": "EFO:0007369", "3-methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia": "EFO:0009014", "Glycine soja": "NCBITaxon:3848", "GM12146": "EFO:0001138", "CS57660": "EFO:0000055", "Legg-Calve-Perthes Disease": "EFO:0007341", "Metaphyseal chondrodysplasia - retinitis pigmentosa": "Orphanet:166035", "desferrioxamine B": "CHEBI:4356", "RC-K8": "EFO:0006742", "GM15510": "EFO:0005347", "response to calcium channel blocker": "EFO:0007767", "NCI-H524": "EFO:0002296", "Juvenile or adult CACH syndrome": "Orphanet:157719", "X-linked intellectual disability, Van Esch type": "Orphanet:163976", "skin and soft tissue Staphylococcus aureus infection": "EFO:1001489", "sarcoma": "EFO:0000691", "129S6": "EFO:0000598", "1 main shoot growth stage": "PO:0007112", "dodecanedioate(2-) {http": "CHEBI:76273", "Atypical Norrie disease due to monosomy Xp11.3": "Orphanet:261501", "Abnormality of the endocrine system": "HP:0000818", "vegetative apex": "EFO:0002519", "CH12.LX": "EFO:0005233", "assay by mass spectrometry": "EFO:0002774", "Sono-Seq": "EFO:0008942", "subthalamic nucleus": "UBERON:0001906", "intrahepatic cholangiocarcinoma": "EFO:1001961", "medulloblastoma": "EFO:0002939", "Microcephaly - deafness - intellectual disability": "Orphanet:2533", "cumulative dose response to bevacizumab": "EFO:0005944", "African iron overload": "Orphanet:139507", "nodular sclerosis Hodgkin lymphoma": "EFO:0004708", "Cerebellar ataxia - hypogonadism": "Orphanet:1173", "Lewy body dementia measurement": "EFO:0006799", "GTL-16": "EFO:0006578", "Melon necrotic spot virus": "NCBITaxon:11987", "carbuncle": "EFO:1000674", "Juvenile Osteochondrosis": "EFO:0008577", "Postaxial polydactyly - dental and vertebral anomalies": "Orphanet:2916", "cholangioma cell": "BTO:0002842", "epidural abscess": "EFO:0007260", "interleukin 1 receptor antagonist measurement": "EFO:0004754", "Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form": "Orphanet:308655", "endocarditis": "EFO:0000465", "Charcot-Marie-Tooth disease type 4": "Orphanet:64749", "Sensorineural hearing impairment": "HP:0000407", "length unit": "UO:0000001", "Familial episodic pain syndrome": "Orphanet:391384", "meninx": "UBERON:0002360", "Syndromic genetic deafness": "Orphanet:90642", "inflammatory bowel disease": "EFO:0003767", "Isovaleric acidemia": "Orphanet:33", "cutaneous melanoma": "EFO:0000389", "OSS": "EFO:0005835", "Methylcobalamin deficiency type cblE": "Orphanet:2169", "thalamus volume": "EFO:0006935", "DDOST-CDG": "Orphanet:300536", "Williams syndrome": "Orphanet:904", "hepatitis virus-related hepatocellular carcinoma": "EFO:0008505", "Bruck syndrome": "Orphanet:2771", "Distal trisomy 4q": "Orphanet:96096", "Synechococcus phage S-IO9": "NCBITaxon:375033", "nutrient": "CHEBI:33284", "Microlissencephaly": "Orphanet:1083", "OVCAR3": "EFO:0003061", "G-361": "EFO:0006394", "Darier disease": "Orphanet:218", "organic cyclic compound metabolic process": "GO:1901360", "ChIP-BS-seq": "EFO:0008685", "WT limb-blood syndrome": "Orphanet:3466", "cysticercosis": "EFO:0007231", "cerebral degeneration": "HP:0007313", "Genetic intestinal polyposis": "Orphanet:363314", "IgG monogalactosylation measurement": "EFO:0008423", "butein": "CHEBI:3237", "a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement": "EFO:0008326", "thallus": "PO:0030027", "goiter": "EFO:0004283", "tepal": "PO:0009033", "Posterior amorphous corneal dystrophy": "Orphanet:98971", "Tricho-oculo-dermo-vertebral syndrome": "Orphanet:3354", "Central polydactyly of fingers": "Orphanet:295004", "HCC2998": "EFO:0005370", "Drosophila yakuba": "NCBITaxon:7245", "medication adherence behavior": "EFO:0006344", "HPL1E": "EFO:0006910", "tectal ventricle": "UBERON:0002289", "Familial visceral myopathy": "Orphanet:2604", "Primary hemophagocytic lymphohistiocytosis": "Orphanet:158038", "Isolated Klippel-Feil syndrome": "Orphanet:2345", "16q24.1 microdeletion syndrome": "Orphanet:352629", "integrin alpha-I": "EFO:0008162", "SGC-7901": "EFO:0006293", "AG11498 {http": "CLO:0021565", "chronic interstitial cystitis": "EFO:1000869", "Epidermolysis bullosa simplex superficialis": "Orphanet:89839", "Sheldon-Hall syndrome": "Orphanet:1147", "Fusarium sporotrichioides": "NCBITaxon:5514", "Aggrecan-related bone disorder": "Orphanet:364817", "portion of meristem tissue {http": "PO:0009013", "Palmoplantar keratoderma-sclerodactyly syndrome": "Orphanet:384", "Pelizaeus-Merzbacher disease, classic form": "Orphanet:280219", "suppressor macrophage": "CL:0000862", "LP.16 sixteen leaves visible stage": "PO:0007119", "Medich giant platelet syndrome": "Orphanet:370127", "Mastomys natalensis": "NCBITaxon:10112", "Cataract - hypertrichosis - intellectual disability": "Orphanet:1375", "Spinal Cord Ischemia": "EFO:1001426", "Inherited ichthyosis": "Orphanet:183435", "SUDHL1": "EFO:0005461", "Laurence-Moon syndrome": "Orphanet:2377", "Histiocytosis": "HP:0100727", "neonatal abstinence syndrome": "EFO:0005799", "CORL279": "EFO:0002143", "Hereditary glaucoma": "Orphanet:359", "hypersplenism": "EFO:1000975", "Cerebral malformation with epilepsy": "Orphanet:166478", "CROAP2": "EFO:0002145", "Spastic paraparesis {http": "HP:0002313", "Hereditary cerebral hemorrhage with amyloidosis, Arctic type": "Orphanet:324723", "Partial deletion of the short arm of chromosome 16": "Orphanet:261956", "Hyper-beta-alaninemia": "Orphanet:309147", "Chronic granulomatous disease": "Orphanet:379", "Populus trichocarpa": "NCBITaxon:3694", "6-pyruvoyl-tetrahydropterin synthase deficiency": "Orphanet:13", "pectoral fin musculature": "ZFA:0000563", "Hamel cerebro-palato-cardiac syndrome": "Orphanet:93946", "Exfoliative ichthyosis": "Orphanet:289586", "Ataxia neuropathy spectrum": "Orphanet:254818", "pulmonary edema": "EFO:1001134", "alveolus of lung": "UBERON:0002299", "Inherited renal cancer-predisposing syndrome": "Orphanet:319328", "triglyceride": "CHEBI:17855", "Oryzias latipes": "NCBITaxon:8090", "Syndromic multisystem autoimmune disease due to Itch deficiency": "Orphanet:228426", "Cerebral disease with cataract": "Orphanet:98645", "anlage": "UBERON:0007688", "Infantile axonal neuropathy": "Orphanet:2679", "Ventriculomegaly {http": "HP:0002119", "Microcebus murinus": "NCBITaxon:30608", "Obesity due to prohormone convertase I deficiency": "Orphanet:71528", "phenylalanine measurement": "EFO:0005001", "NCI-H1618": "EFO:0002258", "Leucoraja erinacea": "NCBITaxon:7782", "unipolar depression": "EFO:0003761", "Disorder of bile acid synthesis": "Orphanet:79168", "Synophrys {http": "HP:0000664", "Isolated Dandy-Walker malformation": "Orphanet:217", "alveolar rhabdomyosarcoma": "EFO:0000248", "renal transplant outcome measurement": "EFO:0005199", "Staphylococcus aureus subsp. aureus RN4220": "NCBITaxon:561307", "dermal dendritic cell": "CL:0001006", "Isolated spina bifida": "Orphanet:823", "nanogram per liter": "EFO:0004382", "glucitol": "CHEBI:30911", "dissection protocol": "EFO:0005519", "dyshidrosis": "EFO:1000688", "Bannayan-Riley-Ruvalcaba syndrome": "Orphanet:109", "carbohydrate": "CHEBI:16646", "sinoatrial nodal reentry tachycardia": "EFO:1001843", "Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement": "Orphanet:90301", "brachial plexus neuritis": "EFO:1000843", "Rheumatic Nodule": "EFO:1001416", "phenylalanine": "CHEBI:28044", "Coloboma of macula - brachydactyly type B": "Orphanet:1471", "superior frontal gyrus grey matter volume measurement": "EFO:0006516", "Lobular Breast Carcinoma In Situ": "EFO:1000326", "Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies": "Orphanet:369897", "ChEC-seq": "EFO:0008682", "Autosomal recessive congenital ichthyosis": "Orphanet:281097", "Langerhans cell sarcoma": "EFO:0007336", "Parotid Gland Squamous Cell Carcinoma": "EFO:1000463", "Malposition of external canthus": "Orphanet:98576", "PLC/PRF/5": "EFO:0006291", "Hereditary motor and sensory neuropathy": "Orphanet:140450", "Non-syndromic respiratory or mediastinal malformation": "Orphanet:108993", "HTR8/SVneo": "EFO:0005709", "2,3-dimethoxynaphthalene-1,4-dione": "CHEBI:64215", "COFS syndrome": "Orphanet:1466", "Familial gastric cancer": "Orphanet:26106", "Autosomal dominant hypocalcemia": "Orphanet:428", "cheekbone morphology measurement": "EFO:0007847", "eye movement measurement": "EFO:0007699", "Hereditary periodic fever syndrome": "Orphanet:324924", "Tay-Sachs disease, B variant, juvenile form": "Orphanet:309185", "mature CD1a-positive dermal dendritic cell": "CL:0002531", "bronchiole": "UBERON:0002186", "Non-distal trisomy 13q": "Orphanet:1702", "Familial papillary renal cell carcinoma": "Orphanet:47044", "Illumina HiSeq 1000": "EFO:0004204", "cardiovascular event measurement": "EFO:0006919", "NCI-H460": "EFO:0003044", "Corneogoniodysgenesis": "Orphanet:98635", "GM15213 {http": "CLO:0027493", "NCI-H2009": "EFO:0002273", "Posterior urethral valve": "Orphanet:93110", "Mosaic monosomy X": "Orphanet:99228", "X-linked myopathy with excessive autophagy": "Orphanet:25980", "glucosamine": "CHEBI:5417", "m1A mapping": "EFO:0008788", "CB4932": "EFO:0004057", "Focal facial dermal dysplasia type III": "Orphanet:1807", "lysobisphosphatidic acid": "CHEBI:60815", "Hs 766T": "EFO:0006590", "Mixed Epithelial Stromal Tumor of the Kidney": "EFO:1000381", "ascorbic acid deficiency": "EFO:1000822", "cataract": "EFO:0001059", "T3b tumor stage": "EFO:0004942", "Agenesis of corpus callosum {http": "HP:0001274", "Syndromic myopia": "Orphanet:98620", "humerus": "UBERON:0000976", "human african trypanosomiasis": "EFO:0005225", "plasma beta-amyloid 1-42 measurement": "EFO:0005660", "Malme3M": "EFO:0002243", "Pedriza ecotype": "EFO:0007609", "interleukin 1 receptor-like 2 measurement": "EFO:0008169", "daytime rest measurement": "EFO:0007828", "posterior cingulate cortex {http": "UBERON:0022353", "2p21 microdeletion syndrome": "Orphanet:163693", "B220-low CD38-positive unswitched memory B cell": "CL:0002116", "ONT PremethION": "EFO:0008634", "Hypotonia - cystinuria syndrome": "Orphanet:163690", "Inherited epidermolysis bullosa": "Orphanet:79361", "sulfate measurement": "EFO:0007864", "Clostridium thermocellum ATCC 27405": "NCBITaxon:203119", "follicular dendritic cell": "CL:0000442", "GM17144 {http": "CLO:0013936", "animal viral hepatitis": "EFO:0007540", "Barrett's esophagus": "EFO:0000280", "Trismus - pseudocamptodactyly": "Orphanet:3377", "Methanobacteria": "NCBITaxon:183925", "Disorder of asparagine metabolism": "Orphanet:391381", "fertilized egg stage": "EFO:0001322", "MARS-seq": "EFO:0008796", "N-cinnamoylglycine {http": "CHEBI:68616", "Natal teeth - intestinal pseudoobstruction - patent ductus": "Orphanet:1654", "Heinz body anemia": "Orphanet:178330", "cell line": "EFO:0000322", "cystatin-SA measurement": "EFO:0008105", "hour": "UO:0000032", "DMS-Seq": "EFO:0008714", "Connective tissue disorder due to lysyl hydroxylase-3 deficiency": "Orphanet:300284", "Robinow-like syndrome": "Orphanet:3105", "balanced reciprocal translocation": "EFO:0004013", "Spinocerebellar ataxia type 36": "Orphanet:276198", "Humeral agenesis/hypoplasia": "Orphanet:294973", "Arthroderma racemosum": "NCBITaxon:231010", "Senior-Loken syndrome": "Orphanet:3156", "ventral hernia": "EFO:1001866", "Autosomal trisomy": "Orphanet:98130", "Non-dystrophic myopathy": "Orphanet:206656", "epidermal Langerhans cell": "CL:0002457", "ganglioneuroma": "EFO:0000500", "Hypomandibular faciocranial dysostosis": "Orphanet:1790", "infectious disease": "EFO:0005741", "N-acetylcarnosine {http": "CHEBI:67249", "relapsing-remitting multiple sclerosis": "EFO:0003929", "Developmental and speech delay due to SOX5 deficiency": "Orphanet:313892", "clear cell sarcoma of the kidney": "EFO:0000350", "Adult hypophosphatasia": "Orphanet:247676", "ST Elevation Myocardial Infarction": "EFO:0008585", "embryo": "UBERON:0000922", "DNA shearing": "EFO:0004189", "D283Med": "EFO:0002156", "bronchial epithelial cell derived cell line": "EFO:0005728", "chronic periodontitis": "EFO:0006343", "Melanocytoma of the Eyeball": "EFO:1000369", "Tursiops truncatus": "NCBITaxon:9739", "Tubular aggregate myopathy": "Orphanet:2593", "chronic childhood arthritis": "EFO:0002609", "xenobiotic": "CHEBI:35703", "GM12815": "EFO:0001158", "Simple Cyst of Kidney": "EFO:0008619", "pharyngula stage": "UBERON:0004707", "Campylobacter": "NCBITaxon:194", "microbiome measurement": "EFO:0007882", "blood cobalt measurement": "EFO:0007577", "pulmonary nodular amyloidosis": "EFO:1001911", "Colorectal Juvenile Polyp": "EFO:1000194", "Synpolydactyly type 2": "Orphanet:295197", "asthenia": "EFO:0007625", "langerin-negative, CD103-negative lymph node dendritic cell": "CL:0002508", "mesectoderm anlage": "FBbt:00000109", "hematological measurement": "EFO:0004503", "external ear": "UBERON:0001691", "CB4857": "EFO:0004056", "fast muscle tissue": "UBERON:0006908", "acetazolamide": "CHEBI:27690", "tag protein fusion library": "EFO:0007565", "chloroplast membrane": "GO:0031969", "Syndromic intestinal malformation": "Orphanet:108969", "polyuria": "HP:0000103", "Autism spectrum disorder-epilepsy-arthrogryposis syndrome": "Orphanet:370943", "Optic atrophy-intellectual disability syndrome": "Orphanet:401777", "protein measurement": "EFO:0004747", "Leukoencephalopathy with mild cerebellar ataxia and white matter edema": "Orphanet:363540", "Porphyromonas gingivalis": "NCBITaxon:837", "homocitrate (3-) {http": "CHEBI:36457", "Saccharum sp.": "NCBITaxon:15819", "Eucalyptus camaldulensis x Eucalyptus grandis": "NCBITaxon:538997", "Rare eyebrow/eyelashes anomaly": "Orphanet:98594", "Perrault syndrome": "Orphanet:2855", "behavioural inhibitory control measurement": "EFO:0008467", "Rohon-Beard neuron": "ZFA:0009150", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency": "Orphanet:404493", "Rhizoctonia solani": "NCBITaxon:456999", "cumulus cell": "CL:0000711", "melanocyte": "CL:0000148", "colon carcinoma": "EFO:1001950", "purine ribonucleotide biosynthetic process": "GO:0009152", "Sillence syndrome": "Orphanet:3168", "Pontocerebellar hypoplasia type 7": "Orphanet:284339", "fulvestrant": "CHEBI:31638", "CD94-negative natural killer cell": "CL:0002447", "Hypoxanthine guanine phosphoribosyltransferase partial deficiency": "Orphanet:79233", "ML-DmD20-c5": "EFO:0005828", "Cystinuria type A": "Orphanet:93612", "phimosis": "EFO:1001104", "renal system process": "GO:0003014", "other organism part": "GO:0044217", "Fc-epsilon RIalpha-low mast cell progenitor": "CL:0002029", "fever": "HP:0001945", "pathogenicity design": "EFO:0001761", "propionylglycine {http": "CHEBI:89836", "Hereditary thrombocytosis with transverse limb defect": "Orphanet:329319", "Gorilla gorilla": "NCBITaxon:9593", "head and neck malignant neoplasia": "EFO:0006859", "ST486": "EFO:0002353", "Splenic Hodgkin Lymphoma": "EFO:1000548", "GM14569 {http": "CLO:0031581", "NLRP12-associated hereditary periodic fever syndrome": "Orphanet:247868", "liquid handler": "OBI:0400112", "Zoarces viviparus": "NCBITaxon:48416", "Recessive intellectual disability - motor dysfunction - multiple joint contractures": "Orphanet:280384", "STRT-seq-2i": "EFO:0008954", "Congenital bile acid synthesis defect type 3": "Orphanet:79302", "Properdin deficiency": "Orphanet:2966", "Bacillus thuringiensis Bt407": "NCBITaxon:527021", "Joint formation defects": "Orphanet:294949", "NCI-H1373": "EFO:0006657", "Pretibial dystrophic epidermolysis bullosa": "Orphanet:79410", "medial": "EFO:0001660", "CS57710": "EFO:0000069", "antimalarial": "CHEBI:38068", "Tc1 cell": "CL:0000917", "amyloid deposition measurement": "EFO:0008351", "breast cancer anti-estrogen resistance protein 3 measurement": "EFO:0008040", "taxane": "CHEBI:36064", "Hepatitis C virus": "NCBITaxon:11103", "Generalized peeling skin syndrome type C": "Orphanet:263558", "Partial duplication of chromosome 2": "Orphanet:262196", "sleep apnea measurement during non-REM sleep": "EFO:0008456", "age": "EFO:0000246", "cellular modification": "EFO:0000325", "J-774 cell": "BTO:0002279", "islet cell tumor": "EFO:0007331", "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency": "Orphanet:319569", "Multiple sulfatase deficiency": "Orphanet:585", "Congenital ectropion": "Orphanet:98570", "Biotinidase deficiency": "Orphanet:79241", "Vibrio alginolyticus": "NCBITaxon:663", "JHH-1": "EFO:0006599", "Cervicothoracic spina bifida aperta": "Orphanet:268397", "ChaGoK1": "EFO:0002155", "embryonic central brain surface glia": "FBbt:00005664", "Ghosal hematodiaphyseal dysplasia": "Orphanet:1802", "Peeling skin syndrome": "Orphanet:817", "Streptomyces antibioticus": "NCBITaxon:1890", "Idiopathic and/or familial pulmonary arterial hypertension": "Orphanet:422", "aldicarb": "CHEBI:2555", "Malformation of the neurenteric canal, spinal cord and column": "Orphanet:268843", "S2-DRSC": "EFO:0005836", "Lactobacillus amylovorus": "NCBITaxon:1604", "nucleotide metabolic process": "GO:0009117", "putamen": "UBERON:0001874", "dorsal root ganglion": "UBERON:0000044", "3-isobutyl-1-methyl-7H-xanthine": "CHEBI:34795", "flucloxacillin": "CHEBI:5098", "bradykinin {http": "CHEBI:3165", "Glomerulonephritis - sparse hair - telangiectasis": "Orphanet:2087", "SCLC-21H": "EFO:0006749", "pyrethroid ester insecticide": "CHEBI:39116", "Glutathione synthetase deficiency without 5-oxoprolinuria": "Orphanet:289849", "polster": "UBERON:2000058", "periventricular leukomalacia": "EFO:1001101", "Cataract - ataxia - deafness": "Orphanet:1368", "Otopalatodigital syndrome type 2": "Orphanet:90652", "Oliver syndrome": "Orphanet:2920", "type II NK T cell secreting interleukin-4": "CL:0000933", "high content screen of cells in treated with a compound library": "EFO:0007553", "SLAF-Seq": "EFO:0008927", "Olivopontocerebellar atrophy - deafness": "Orphanet:2732", "common bile duct neoplasm": "EFO:1000876", "Plasmodium falciparum antigen IgG1 measurement": "EFO:0007810", "CB491": "EFO:0004049", "Distal trisomy 5q": "Orphanet:96097", "Porokeratosis of Mibelli": "Orphanet:735", "Congenital disorder of glycosylation with skin involvement": "Orphanet:371200", "Weissella confusa": "NCBITaxon:1583", "AG09699 {http": "CLO:0021913", "acute monocytic leukemia": "EFO:0000221", "OCI-LY1": "EFO:0005907", "Multiple acyl-CoA dehydrogenation deficiency, mild type": "Orphanet:394532", "vegetating cicatricial pemphigoid": "EFO:0008612", "hypopigmentation of eyelid": "EFO:1000713", "Enteromyxum leei": "NCBITaxon:188704", "calcium ion homeostasis": "GO:0055074", "4-\\\\\\{[(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)carbonyl]amino\\\\\\}benzoic acid": "CHEBI:64210", "Autosomal dominant Opitz G/BBB syndrome": "Orphanet:306588", "Methylmalonic acidemia with homocystinuria": "Orphanet:26", "microgram per day": "EFO:0004378", "Human T-lymphotropic virus 2 infectious disease": "EFO:1001349", "Lathosterolosis": "Orphanet:46059", "Polyomavirus infectious disease": "EFO:0007451", "Medullary Cystic Kidney Disease Type II": "EFO:0008618", "NCI-H1048": "EFO:0002248", "Spectrin-associated autosomal recessive cerebellar ataxia": "Orphanet:352403", "Selective IgM deficiency": "Orphanet:331235", "Sialidosis type 1": "Orphanet:812", "peanut allergy measurement": "EFO:0007017", "mean fractional anisotropy measurement": "EFO:0008399", "Brown-Sequard Syndrome": "EFO:1001279", "cystic renal cell carcinoma": "EFO:0006388", "body height": "EFO:0004339", "addictive behaviour": "EFO:0004347", "retroarticular": "UBERON:2000422", "optic nerve neoplasm": "EFO:1001073", "Charcot-Marie-Tooth disease type 4D": "Orphanet:99950", "N(2),N(2)-dimethylguanosine {http": "CHEBI:19289", "cholinergic urticaria": "EFO:1000679", "plant nutrient treatment {http": "EO:0007241", "5-fluorouridine": "CHEBI:185922", "bacterial vaginosis": "EFO:0003932", "Adenosine monophosphate deaminase deficiency": "Orphanet:45", "acute lung injury": "EFO:0004610", "Rare genetic cardiac disease": "Orphanet:98054", "mesenteric lymph node": "UBERON:0002509", "Sulfation-related bone disorder": "Orphanet:93423", "Papillary Tumor of the Pineal Region": "EFO:1000451", "Congenital tracheal stenosis": "Orphanet:141127", "serum alpha-1-antitrypsin measurement": "EFO:0005415", "GM17256 {http": "CLO:0014396", "Early-onset cerebellar ataxia with retained tendon reflexes": "Orphanet:1177", "Hemochromatosis type 2": "Orphanet:79230", "Ulna metaphyseal dysplasia syndrome": "Orphanet:1837", "cerebral malaria": "EFO:0006857", "ulcerative colitis": "EFO:0000729", "red blood cell density measurement": "EFO:0007978", "hematopoietic multipotent progenitor cell": "CL:0000837", "Mycobacterium bovis BCG str. Pasteur 1173P2": "NCBITaxon:410289", "atmosphere unit": "EFO:0005212", "6q25 microdeletion syndrome": "Orphanet:251056", "3-methylglutaconic aciduria type 1": "Orphanet:67046", "Genetic porokeratosis": "Orphanet:183444", "ILSXISS100/TejJ": "EFO:0003003", "8-bromo-3',5'-cyclic AMP": "CHEBI:64211", "Tessier number 6 facial cleft": "Orphanet:141265", "Creutzfeldt Jacob Disease": "EFO:0004226", "PAT\u00e2\u0080\u0093ChIP": "EFO:0008852", "10q22.3q23.3 microdeletion syndrome": "Orphanet:276413", "CLN5 disease": "Orphanet:228360", "J185a {http": "EFO:0005486", "ostertagiasis": "EFO:0007414", "Carney complex": "Orphanet:1359", "CINCA syndrome": "Orphanet:1451", "N-acetyl-L-alanine {http": "CHEBI:40992", "JT709": "EFO:0004088", "root cap": "PO:0020123", "Caco-2/TC7": "EFO:0002817", "childhood onset asthma": "EFO:0004591", "quinolinate(2-) {http": "CHEBI:29959", "Polymicrogyria": "Orphanet:35981", "severe acute respiratory syndrome": "EFO:0000694", "response to temozolomide": "GO:1990054", "Acro-pectoral syndrome": "Orphanet:85203", "kallikrein-7 measurement": "EFO:0008195", "taxonomic microbiome measurement": "EFO:0007883", "Congenital generalized hypertrichosis, Ambras type": "Orphanet:1023", "mediastinal lymph node": "UBERON:0002524", "Mel-2183": "EFO:0005706", "metalloproteinase inhibitor 3 measurement": "EFO:0008231", "Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency": "Orphanet:91135", "gum cancer": "EFO:0005557", "prognostic subgroup": "EFO:0000672", "Rare disorder with dystonia and other neurologic or systemic manifestation": "Orphanet:370106", "visual cortical surface area measurement": "EFO:0004771", "folic acid metabolic process": "GO:0046655", "Thymic Undifferentiated Carcinoma": "EFO:1000580", "Rhizomelic syndrome, Urbach type": "Orphanet:3098", "N-methyl-L-alanine {http": "CHEBI:17519", "male homosexuality": "EFO:0008486", "BV173": "EFO:0002118", "Bar-Seq": "EFO:0008654", "Gonadal Teratoma": "EFO:1000282", "Pool-Seq": "EFO:0008867", "6q terminal deletion syndrome": "Orphanet:75857", "Chromosome Y structural anomaly": "Orphanet:98158", "osteitis deformans": "EFO:0004261", "extracellular vesicular exosome": "GO:0070062", "Endocrine-cerebro-osteodysplasia syndrome": "Orphanet:199332", "LP.09 nine leaves visible": "PO:0007101", "Qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase -": "Orphanet:209203", "gastrointestinal inflammation": "HP:0004386", "NCI-H510A": "EFO:0006693", "Ara-C-resistant murine leukemia": "EFO:0002032", "large intestine primordium": "FBbt:00005505", "cholic acid": "CHEBI:16359", "Early pro-B cell": "CL:0002046", "anterior endoderm anlage": "FBbt:00000210", "Streptomyces coelicolor A3(2)": "NCBITaxon:100226", "response to sertraline": "EFO:0006327", "spleen cancer": "EFO:0007491", "Hypogonadotrophic hypogonadism {http": "HP:0000044", "Cleft lip/palate - intestinal malrotation - cardiopathy": "Orphanet:2001", "crystal cell": "CL:0000392", "EBC-1": "EFO:0003115", "CMRF35-like molecule 6 measurement": "EFO:0008086", "Progressive muscular dystrophy": "Orphanet:206644", "Familial hypocalciuric hypercalcemia type 3": "Orphanet:101050", "Behr syndrome": "Orphanet:1239", "long term hematopoietic stem cell": "CL:0002034", "biliary liver cirrhosis": "EFO:0004267", "copper(2+) sulfate": "CHEBI:23414", "Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells": "Orphanet:331240", "shell of nucleus accumbens": "UBERON:0012171", "PC-7": "EFO:0002846", "Curcuma longa": "NCBITaxon:136217", "urinary albumin excretion rate": "EFO:0005667", "DR40": "EFO:0004082", "Pyruvate dehydrogenase E3 deficiency": "Orphanet:2394", "limited phosphate treatment {http": "EO:0001046", "Arterio-Arterial Fistula": "EFO:1001270", "spleen": "UBERON:0002106", "Infantile muscular hypotonia {http": "HP:0008947", "Episodic ataxia type 1": "Orphanet:37612", "Benign Smooth Muscle Neoplasm": "EFO:1000121", "Intestinal disease due to vitamin absorption anomaly": "Orphanet:104004", "congenital disorder of glycosylation type II": "EFO:0005546", "Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11": "Orphanet:96193", "Spondylocarpotarsal synostosis": "Orphanet:3275", "Hypothyroidism due to TSH receptor mutations": "Orphanet:90673", "HT": "EFO:0002200", "ATRFLOX": "EFO:0006535", "GM17192 {http": "CLO:0013796", "DDT metabolite measurement": "EFO:0007886", "Epileptic encephalopathy with global cerebral demyelination": "Orphanet:353217", "sulforaphane": "CHEBI:47807", "Pan troglodytes": "NCBITaxon:9598", "leaf base {http": "PO:0020040", "ALG12-CDG": "Orphanet:79324", "Self-healing collodion baby": "Orphanet:281122", "ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement": "EFO:0008014", "lepromatous leprosy": "EFO:0001057", "Mandibuloacral dysplasia with type B lipodystrophy": "Orphanet:90154", "Disorder of mitochondrial fatty acid oxidation": "Orphanet:309115", "GM17735 {http": "CLO:0017046", "tumor necrosis factor-alpha measurement": "EFO:0004684", "Hirschsprung disease": "Orphanet:388", "symptomatic heart failure": "EFO:0003146", "Cherubism": "Orphanet:184", "Heavy Chain Disease": "EFO:1001341", "Hypermethioninemia due to glycine N-methyltransferase deficiency": "Orphanet:289891", "Autosomal dominant Charcot-Marie-Tooth disease type 2A2": "Orphanet:99947", "hemolytic anemia": "EFO:0005558", "Purpura Fulminans": "EFO:1001913", "dense area measurement": "EFO:0006503", "Human papillomavirus": "NCBITaxon:10566", "contagious pleuropneumonia": "EFO:0007221", "Illumina MiSeq standard manufacturer's protocol": "EFO:0005087", "caudal ganglionic eminence": "UBERON:0004026", "Congenital enterocyte heparan sulfate deficiency": "Orphanet:103910", "3-dehydroteasterone": "CHEBI:20000", "Severe combined immunodeficiency due to adenosine deaminase deficiency": "Orphanet:277", "BL41K3": "EFO:0001091", "Maternal uniparental disomy of chromosome 13": "Orphanet:97678", "Qualitative or quantitative defects of TRIM32": "Orphanet:207107", "Rapture": "EFO:0008881", "non-alcoholic fatty liver": "EFO:1001248", "JMP syndrome": "Orphanet:324999", "Uncombable hair syndrome": "Orphanet:1410", "granulocyte count": "EFO:0007987", "aortic valve calcification": "EFO:0005239", "Omphalocele syndrome, Shprintzen-Goldberg type": "Orphanet:3164", "Vesicular stomatitis Indiana virus": "NCBITaxon:11277", "Combined cervical dystonia": "Orphanet:370114", "chemotherapy-induced oral mucositis": "EFO:0006313", "Blount disease": "Orphanet:2768", "angiopoietin-2 measurement": "EFO:0006901", "methyl beta-D-glucopyranoside {http": "CHEBI:320055", "Total autosomal monosomy": "Orphanet:98141", "soft tissue sarcoma": "EFO:1001968", "Mesomelic dwarfism - cleft palate - camptodactyly": "Orphanet:2631", "Partial deletion of the short arm of chromosome 18": "Orphanet:261974", "vein": "UBERON:0001638", "response to gemcitabine": "GO:0036272", "X-linked dominant chondrodysplasia, Chassaing-Lacombe type": "Orphanet:163966", "Chronic respiratory distress with surfactant metabolism deficiency": "Orphanet:217566", "pancreactic component": "EFO:0003861", "Congenital trochlear nerve palsy": "Orphanet:98686", "Insulin-resistance syndrome type A": "Orphanet:2297", "Dengue Hemorrhagic Fever": "EFO:0004227", "MCF-7aro": "EFO:0002072", "ND00151 {http": "CLO:0030688", "Eye Injuries, Penetrating": "EFO:1001323", "thymic conventional dendritic cell": "CL:0000941", "Arabidopsis lyrata subsp. petraea": "NCBITaxon:59691", "Streptococcus pyogenes MGAS5005": "NCBITaxon:293653", "female fertility": "EFO:0006918", "DNA methylation": "GO:0006306", "Aspergillus fumigatus Af293": "NCBITaxon:330879", "RKN": "EFO:0006745", "HMY-1": "EFO:0006582", "Progressive retinal dystrophy due to retinol transport defect": "Orphanet:352718", "Hypertelorism {http": "HP:0000316", "NCI-H446": "EFO:0002293", "anaplastic large cell lymphoma": "EFO:0003032", "caMAB-seq": "EFO:0008670", "methyl filtration": "EFO:0004169", "GM12892": "EFO:0002786", "larval day 14-20": "EFO:0001307", "Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency": "Orphanet:319563", "sphenoid sinusitis": "EFO:0007489", "placode": "EFO:0001650", "Alport syndrome - intellectual disability - midface hypoplasia - elliptocytosis": "Orphanet:86818", "Carbamoyl-phosphate synthase deficiency": "Orphanet:147", "Pyrus communis": "NCBITaxon:23211", "Amish infantile epilepsy syndrome": "Orphanet:171714", "ritanserin": "CHEBI:64195", "sleep latency": "EFO:0005280", "susceptibility to Mycobacterium tuberculosis infection measurement": "EFO:0008407", "Banki syndrome": "Orphanet:1228", "Neurometabolic disease": "Orphanet:68385", "swim bladder": "UBERON:0006860", "Actinobacillus pleuropneumoniae serovar 3": "NCBITaxon:434270", "magnesium deficiency": "EFO:1001029", "Congenital muscular dystrophy with cerebellar involvement": "Orphanet:370959", "Autosomal recessive spastic paraplegia type 69": "Orphanet:401830", "gamma-Glu-Gln {http": "CHEBI:73707", "Hypophthalmichthys molitrix": "NCBITaxon:13095", "embryonic hindgut": "FBbt:00005630", "eccrine sweat gland cancer": "EFO:0005553", "Peutz-Jeghers Polyp of the Stomach": "EFO:1000471", "parental longevity": "EFO:0007796", "immature neutrophil": "CL:0000776", "DR1564": "EFO:0004084", "Exercise-induced hyperinsulinism": "Orphanet:165991", "2-linoleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:76084", "fenazaquin": "CHEBI:38593", "Multiple synostoses syndrome": "Orphanet:3237", "Rickettsia prowazekii Rp22": "NCBITaxon:449216", "HCC1493": "EFO:0006427", "Congenital hereditary facial paralysis with variable hearing loss": "Orphanet:306530", "left ventricular ejection fraction measurement": "EFO:0008373", "Kindler syndrome": "Orphanet:2908", "Pure or complex autosomal recessive spastic paraplegia": "Orphanet:320346", "antennal disc": "UBERON:6001767", "lymph node macrophage": "CL:0000868", "Accessory pancreas": "Orphanet:674", "Atypical Lobular Breast Hyperplasia": "EFO:1000100", "morphology": "PATO:0000051", "X-linked lymphoproliferative disease": "Orphanet:2442", "subphrenic abscess": "EFO:1001854", "carotid artery thrombosis": "EFO:1000853", "genotype": "EFO:0000513", "recombination measurement": "EFO:0005919", "hardware variation design": "EFO:0001767", "GABAergic neuron": "CL:0000617", "Brachymorphism - onychodysplasia - dysphalangism": "Orphanet:1292", "CD8_alpha-positive plasmactyoid dendritic cell": "CL:0002456", "Maternal uniparental disomy of chromosome 9": "Orphanet:96183", "Cataract - intellectual disability - anal atresia - urinary defects": "Orphanet:1381", "plasma cell neoplasm": "EFO:0000200", "smooth endoplasmic reticulum": "GO:0005790", "hemopericardium": "EFO:0007298", "pulmonary mucoepidermoid carcinoma": "EFO:0006740", "Spea bombifrons": "NCBITaxon:233779", "Irish": "EFO:0003163", "GM2-gangliosidosis, AB variant": "Orphanet:309246", "joule per square meter": "EFO:0004414", "embryonic stage 15": "EFO:0005875", "amnioserosa primordium": "FBbt:00017000", "lymph node": "UBERON:0000029", "Picornaviridae infectious disease": "EFO:0007438", "ventral hyoid arch": "UBERON:0011153", "Drosophila persimilis": "NCBITaxon:7234", "Citrullinemia type II": "Orphanet:247585", "Polydactyly of a triphalangeal thumb, unilateral": "Orphanet:295148", "valproic acid": "CHEBI:39867", "orbital cancer": "EFO:0007408", "pseudouridine {http": "CHEBI:17802", "Ws-2": "EFO:0005158", "HGF": "EFO:0002792", "Polysyndactyly, unilateral": "Orphanet:295159", "Congenital dyserythropoietic anemia": "Orphanet:85", "GM17241 {http": "CLO:0014411", "Spinal muscular atrophy associated with central nervous system anomaly": "Orphanet:207012", "Conjunctival tumor": "Orphanet:98616", "cardiac conduction defect": "EFO:1001497", "delayed reward discounting measurement": "EFO:0008476", "HPAF1": "EFO:0006279", "Familial nonmedullary thyroid carcinoma": "Orphanet:319494", "Hypohidrotic ectodermal dysplasia": "Orphanet:238468", "type II diabetes mellitus with acanthosis nigricans": "EFO:1001503", "Congenital myopathy with cores": "Orphanet:172976", "Echinochloa glabrescens {http": "NCBITaxon:1292002", "hyoid muscle": "UBERON:0005493", "auxin role": "CHEBI:22676", "Hemimegalencephaly": "Orphanet:99802", "binge eating": "EFO:0005924", "Hearing loss - familial salivary gland insensitivity to aldosterone": "Orphanet:3225", "Stickler syndrome": "Orphanet:828", "pericoronitis": "EFO:1001098", "homeostatic process": "GO:0042592", "SW900": "EFO:0002374", "aminosilane substrate coating": "EFO:0005070", "Mus spretus": "NCBITaxon:10096", "ophthalmic herpes zoster": "EFO:0007403", "milliliter per liter": "UO:0000207", "Ring chromosome 14": "Orphanet:1440", "NUGC-4": "EFO:0006703", "LbetaT2": "EFO:0002070", "Primary ciliary dyskinesia - retinitis pigmentosa": "Orphanet:247522", "refractory anemia with excess blasts": "EFO:0003811", "X-linked intellectual disability, Stevenson type": "Orphanet:85325", "Maple syrup urine disease": "Orphanet:511", "Dejerine-Sottas syndrome": "Orphanet:64748", "Zoster Sine Herpete": "EFO:1001453", "Neurodegenerative disease with chorea": "Orphanet:306719", "embryonic cell": "CL:0002321", "experimental cell": "EFO:0002958", "Plasmodium chabaudi chabaudi": "NCBITaxon:31271", "Hepadnaviridae infectious disease": "EFO:0007301", "early T lineage precursor": "CL:0002425", "strongyloidiasis": "EFO:0007501", "skeletal muscle tissue": "UBERON:0001134", "asthma": "EFO:0000270", "Feingold syndrome": "Orphanet:1305", "Familial paroxysmal ataxia": "Orphanet:97", "Methanosarcina barkeri": "NCBITaxon:2208", "blood toxic metal measurement": "EFO:0007574", "adrenergic uptake inhibitor": "CHEBI:35640", "frontal theta oscillation measurement": "EFO:0004800", "Macrodactyly of fingers, unilateral": "Orphanet:295239", "very low density lipoprotein cholesterol measurement": "EFO:0008317", "cryoglobulinemia": "EFO:0005846", "ILSXISS62/TejJ": "EFO:0002990", "female gonad": "UBERON:0000992", "HUES63": "EFO:0007088", "acetyltaurine {http": "CHEBI:84415", "Blue rubber bleb nevus": "Orphanet:1059", "Entamoeba histolytica": "NCBITaxon:5759", "Rabson-Mendenhall syndrome": "Orphanet:769", "Glycogen storage disease due to glycogen debranching enzyme deficiency": "Orphanet:366", "GM17288 {http": "CLO:0013080", "alpha wave measurement": "EFO:0006870", "Familial isolated hypoparathyroidism due to impaired PTH secretion": "Orphanet:189466", "flavin adenine dinucleotide {http": "CHEBI:24040", "Acral peeling skin syndrome": "Orphanet:263534", "cDNA library construction": "EFO:0004187", "chordamesoderm": "UBERON:0004880", "Blanes ecotype": "EFO:0005166", "HS578T": "EFO:0001192", "MRI defined brain infarct": "EFO:0004715", "CS57847": "EFO:0000143", "C-X-C motif chemokine 5 measurement": "EFO:0008058", "Orofaciodigital syndrome type 11": "Orphanet:141000", "embryonic stem cell derived neuronal stem cell": "EFO:0002968", "ILSXISS50/TejJ": "EFO:0002986", "Lipoyl transferase 1 deficiency": "Orphanet:401862", "Heterodera glycines": "NCBITaxon:51029", "nutraceutical": "CHEBI:50733", "hereditary nephritis": "EFO:0004128", "lower leg skin": "UBERON:0004264", "Mosaic trisomy 17": "Orphanet:1711", "ZF4": "EFO:0001261", "prostate gland": "UBERON:0002367", "Acrogeria": "Orphanet:2500", "cerebrovascular disorder": "EFO:0003763", "Pyrococcus furiosus": "NCBITaxon:2261", "orbital plasma cell granuloma": "EFO:1001077", "vanillate {http": "CHEBI:16632", "exome": "EFO:0004422", "calf": "FMA:24984", "Waardenburg-Shah syndrome": "Orphanet:897", "myeloproliferative disorder": "EFO:0004251", "embryonic corpus allatum": "EFO:0000448", "FL.01 1/4 of flowers open stage": "EFO:0005793", "erythrocyte cadmium measurement": "EFO:0007807", "Distal spinal muscular atrophy": "Orphanet:206713", "Listeria innocua": "NCBITaxon:1642", "Anonychia {http": "HP:0001798", "macrophage colony stimulating factor measurement": "EFO:0008217", "pulmonary blastoma": "EFO:0007458", "Familial pseudohyperkalemia": "Orphanet:90044", "(R)-3-phenyllactate {http": "CHEBI:11009", "ES cell line": "EFO:0003074", "CS57722": "EFO:0000075", "STATseq": "EFO:0008951", "mantle cell": "EFO:1001468", "Sphingomonas sp. NM05": "NCBITaxon:352164", "X-linked intellectual disability, Siderius type": "Orphanet:85287", "Rare genetic neurological disorder": "Orphanet:71859", "Sturge-Weber syndrome": "Orphanet:3205", "cyclooxygenase inhibitor": "CHEBI:35544", "abnormality of the musculature": "HP:0003011", "response to platinum-based neoadjuvant chemotherapy": "EFO:0007943", "iminodiacetate {http": "CHEBI:24785", "Mitochondrial DNA depletion syndrome, myopathic form": "Orphanet:254875", "CA46": "EFO:0002124", "tumor necrosis factor-inducible gene 6 protein measurement": "EFO:0008311", "Autosomal recessive spastic paraplegia type 71": "Orphanet:401840", "Congenital dyserythropoietic anemia type III": "Orphanet:98870", "M6A-RIP": "EFO:0008789", "emphysematous cholecystitis": "EFO:0007249", "Alpha-mannosidosis, infantile form": "Orphanet:309282", "naphthalene": "CHEBI:16482", "Glomus Jugulare Tumor": "EFO:1001796", "Fibrochondrogenesis": "Orphanet:2021", "free androgen index": "EFO:0007005", "white matter hyperintensity measurement": "EFO:0005665", "Pomacentrus moluccensis": "NCBITaxon:80956", "visceral abdominal adipose tissue": "UBERON:0014454", "leaf tip": "PO:0025142", "Postaxial polydactyly type B, bilateral": "Orphanet:295169", "insulin secretion rate measurement": "EFO:0008001", "Geranium dissectum": "NCBITaxon:326028", "N stage": "EFO:0004927", "ovarian carcinoma": "EFO:0001075", "SNU1": "EFO:0002343", "annexin A2 measurement": "EFO:0008027", "Weismann-Netter syndrome": "Orphanet:3344", "early gestational weight gain": "EFO:0008437", "Inborn errors of metabolism": "Orphanet:68367", "Spinocerebellar ataxia type 38": "EFO:0009056", "Rare disease with thoracic aortic aneurysm and aortic dissection": "Orphanet:285014", "Spinocerebellar ataxia type 8": "Orphanet:98760", "limited scleroderma": "EFO:1001017", "Lactobacillus paracasei": "NCBITaxon:1597", "Mitochondrial DNA depletion syndrome, encephalomyopathic form": "Orphanet:254803", "Actinobacillus pleuropneumoniae serovar 5": "NCBITaxon:44294", "embryonic day 11.5": "EFO:0002562", "cervical cancer cell line": "BTO:0001967", "Schistosoma mansoni": "NCBITaxon:6183", "macrophage dendritic cell progenitor": "CL:0002009", "(1R,3S)-3-(adamantan-1-yl)-1-(aminomethyl)-3,4-dihydroisochromene-5,6-diol hydrochloride": "CHEBI:64078", "Liddle syndrome": "Orphanet:526", "CaptureSeq": "EFO:0008675", "mixed sex population": "EFO:0001271", "blastula 128-cell": "EFO:0001273", "Crouzon disease": "Orphanet:207", "Bulbospinal muscular atrophy": "Orphanet:206701", "PRO-cap": "EFO:0008868", "Asian Indian": "EFO:0003153", "non-high density lipoprotein cholesterol measurement": "EFO:0005689", "nanogram per microliter": "EFO:0004383", "Tubular renal disease - cardiomyopathy": "Orphanet:73224", "short sleep": "EFO:0004807", "Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency": "Orphanet:79240", "3-methylxanthine {http": "CHEBI:62205", "Australian bat lyssavirus": "NCBITaxon:90961", "plant egg": "CL:0000025", "Oculodental syndrome, Rutherfurd type": "Orphanet:2709", "temporal lobe epilepsy": "EFO:0000773", "MOLT-4": "EFO:0001220", "Waardenburg syndrome type 2": "Orphanet:895", "family history of lung cancer": "EFO:0006953", "pyrenocyte": "CL:0002358", "antidepressant-induced sexual dysfunction": "EFO:0006322", "CD34-positive, CD38-positive granulocyte monocyte progenitor": "CL:0002001", "IgG/IgA pemphigus": "EFO:0008605", "Brittle cornea syndrome": "Orphanet:90354", "linoleic acid measurement": "EFO:0006807", "doxorubicin": "CHEBI:28748", "Congenital factor XIII deficiency": "Orphanet:331", "Non-syndromic visceral malformation": "Orphanet:108971", "Frontotemporal dementia with motor neuron disease": "Orphanet:275872", "3-hydroxy-3-methylglutaric acid {http": "CHEBI:16831", "Lysosomal glycogen storage disease": "Orphanet:309337", "Pili torti": "Orphanet:2889", "phosphate ion homeostasis": "GO:0055062", "Congenital myopathy": "Orphanet:97245", "glycine betaine {http": "CHEBI:17750", "adipocyte of breast": "CL:0002617", "macrophage migration inhibitory factor measurement": "EFO:0008221", "Rhipicephalus microplus": "NCBITaxon:6941", "leaf sheath": "PO:0020104", "language impairment": "EFO:0005425", "uterine fibroid": "EFO:0000731", "Activated PIK3-delta syndrome": "Orphanet:397596", "ossification of the posterior longitudinal ligament of the spine": "EFO:0005895", "Vaginal Melanoma": "EFO:1000619", "Lymphocytic choriomeningitis virus": "NCBITaxon:11623", "skin of pelvis": "UBERON:0001415", "receptacle {http": "PO:0009064", "Gr1-high myeloid suppressor cell": "CL:0002467", "Microphthalmia with linear skin defects syndrome": "Orphanet:2556", "psychosis": "EFO:0005407", "Triphalangeal thumbs - brachyectrodactyly": "Orphanet:2947", "Partial cryptophthalmia": "Orphanet:98950", "COR-L47": "EFO:0006556", "ribonucleoside metabolic process": "GO:0009119", "drug": "CHEBI:23888", "proliferating embryo Ce": "EFO:0005501", "Juvenile Huntington disease": "Orphanet:248111", "aspirin induced asthma": "HP:0012042", "Autosomal recessive limb-girdle muscular dystrophy type 2L": "Orphanet:206549", "Diaphanospondylodysostosis": "Orphanet:66637", "Festuca rubra subsp. littoralis": "NCBITaxon:98755", "ovarian adenocarcinoma": "EFO:0006460", "Rare genetic intellectual disability": "Orphanet:183757", "Megalocornea-intellectual disability syndrome": "Orphanet:2479", "GM17285 {http": "CLO:0013090", "myeloid white cell count": "EFO:0007988", "CB6F1": "EFO:0001339", "4-(4-methylpiperazin-1-yl)-7-(trifluoromethyl)pyrrolo[1,2-a]quinoxaline dimaleate": "CHEBI:64053", "INA-6": "EFO:0005386", "N-benzyladenine": "CHEBI:29022", "Renal tubular dysgenesis of genetic origin": "Orphanet:97369", "Human herpesvirus 1": "NCBITaxon:10298", "Autosomal recessive spastic paraplegia type 35": "Orphanet:171629", "temporal arteritis": "EFO:1001209", "Maternal uniparental disomy of chromosome 21": "Orphanet:96187", "Pyruvate dehydrogenase E2 deficiency": "Orphanet:79244", "Theiler stage 20": "EFO:0004410", "abnormality of brain morphology {http": "HP:0012443", "Junctional epidermolysis bullosa": "Orphanet:305", "langerin-positive lymph node dendritic cell": "CL:0002507", "GM07056": "EFO:0001114", "Polydactyly": "Orphanet:2913", "Otopalatodigital syndrome": "Orphanet:669", "osteoprotegerin measurement": "EFO:0005918", "acetic acid": "CHEBI:15366", "O-linoleyl-L-carnitine {http": "CHEBI:84098", "thiopurine immunosuppressant-induced pancreatitis": "EFO:0006315", "monogenic diabetes": "EFO:1001511", "Spinocerebellar ataxia type 42": "EFO:0009059", "Bifunctional enzyme deficiency": "Orphanet:300", "apical": "EFO:0001653", "NCI-H2171": "EFO:0002282", "cotinine N-oxide {http": "CHEBI:89087", "iPS-20b": "EFO:0007108", "Atrial septal defect, ostium primum type": "Orphanet:99106", "skeletal muscle myoblast": "CL:0000515", "alcohol and nicotine codependence": "EFO:0004776", "Leishmania infantum": "NCBITaxon:5671", "Nephrogenic diabetes insipidus - intracranial calcification": "Orphanet:3145", "Populus tremula": "NCBITaxon:113636", "internal carotid artery": "UBERON:0001532", "icSHAPE": "EFO:0008775", "17q12 microdeletion syndrome": "Orphanet:261265", "Partial duplication of the long arm of chromosome 15": "Orphanet:262950", "RAPADILINO syndrome": "Orphanet:3021", "ciglitazone": "CHEBI:64227", "NOD/ShiLtJ": "EFO:0007736", "Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome": "Orphanet:391376", "picometer": "UO:0000020", "GM19099": "EFO:0005350", "Male infertility due to large-headed multiflagellar polyploid spermatozoa": "Orphanet:137893", "Aspergillus carbonarius": "NCBITaxon:40993", "white matter microstructure measurement": "EFO:0005674", "HUES53": "EFO:0007085", "Abnormal blistering of the skin {http": "HP:0008066", "Perlecan-related bone disorder": "Orphanet:93424", "cell concentration unit": "UO:0000200", "Desulfovibrio vulgaris str. Hildenborough": "NCBITaxon:882", "Zea mays cv. B73": "EFO:0007022", "Synechococcus phage S-IO21": "NCBITaxon:375052", "GM17140 {http": "CLO:0013935", "Congenital disorder of glycosylation with nephropathy as a major feature": "Orphanet:371207", "PAGOD syndrome": "Orphanet:991", "GM17106 {http": "CLO:0014902", "activated CD4-positive, alpha-beta T cell": "CL:0000896", "urinary uromodulin measurement": "EFO:0005663", "Stapes ankylosis with broad thumbs and toes": "Orphanet:140917", "Phaseolus vulgaris": "NCBITaxon:3885", "jejunum": "UBERON:0002115", "Combined immunodeficiency with facio-oculo-skeletal anomalies": "Orphanet:221139", "information entity": "IAO:0000030", "nucellus {http": "PO:0020020", "Fatal post-viral neurodegenerative disorder": "Orphanet:391343", "lung cancer cell line": "EFO:0002934", "choledocholithiasis": "EFO:1000865", "Ovarian Leydig Cell Tumor": "EFO:1000423", "amyotrophic lateral sclerosis": "EFO:0000253", "Genetic cerebrovascular dementia": "Orphanet:371439", "nephrosclerosis": "EFO:1000041", "investigator": "EFO:0001739", "OCI-AML3": "EFO:0006289", "Ring chromosome 12": "Orphanet:1439", "Ehlers-Danlos syndrome, cardiac valvular type": "Orphanet:230851", "Micrognathia {http": "HP:0000347", "CD38-negative naive B cell": "CL:0002102", "Leydig Cell Tumor": "EFO:1000321", "core of nucleus accumbens": "UBERON:0012170", "Antisynthetase syndrome": "EFO:1001982", "Congenital intestinal disease due to an enzymatic defect": "Orphanet:104006", "ionomycin": "CHEBI:63954", "Disorder of pyrimidine metabolism": "Orphanet:79193", "F4/80-negative adipose macrophage": "CL:0002478", "Rare strabismus and restriction syndrome": "Orphanet:98681", "diabetic retinopathy": "EFO:0003770", "rectal adenocarcinoma": "EFO:0005631", "CS57753": "EFO:0000088", "Rare genetic systemic or rheumatologic disease": "Orphanet:271870", "CS57901": "EFO:0000161", "Adie syndrome": "EFO:0004126", "Autosomal recessive limb-girdle muscular dystrophy type 2S": "Orphanet:369840", "Rolandic epilepsy": "Orphanet:1945", "bacterial nucleoid": "GO:0043590", "cell division": "GO:0051301", "animal developmental tissue": "EFO:0000795", "GM17757 {http": "CLO:0016606", "Trypanosoma vivax": "NCBITaxon:5699", "Malformation syndrome with connective tissue involvement": "Orphanet:139030", "streptococcal infection": "EFO:1001476", "Rare genetic headache": "Orphanet:183509", "B220-positive CD38-positive unswitched memory B cell": "CL:0002115", "phloem {http": "PO:0005417", "KIF5": "EFO:0002712", "Congenital cataract, Volkmann type": "Orphanet:98983", "Trisomy 4p": "Orphanet:1738", "Dwarfism - intellectual disability - eye abnormality": "Orphanet:2650", "Sparus aurata": "NCBITaxon:8175", "proximal portion of anterior interventricular branch of left coronary artery": "FMA:3866", "basibranchial bone": "UBERON:0004740", "Emanuel syndrome": "Orphanet:96170", "Pelger-Huet anomaly": "EFO:1001093", "Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis": "Orphanet:93279", "smooth muscle": "EFO:0000889", "GM07345": "EFO:0001115", "presumptive shield": "UBERON:0007283", "Callorhinchus milii": "NCBITaxon:7868", "absent or delayed speech development": "EFO:0009083", "16p11.2p12.2 microdeletion syndrome": "Orphanet:261211", "Familial Dupuytren contracture": "Orphanet:79142", "MN1": "EFO:0007601", "Ataxia with dementia": "Orphanet:98538", "Papillon-Lef\u00c3\u00a8vre syndrome": "Orphanet:678", "sinusitis": "EFO:0007486", "Intellectual disability - obesity - brain malformations - facial dysmorphism": "Orphanet:352530", "Prunus necrotic ringspot virus": "NCBITaxon:37733", "all-cis-octadeca-6,9,12,15-tetraenoic acid {http": "CHEBI:32389", "whole plant fruit ripening complete stage {http": "PO:0007038", "Young syndrome": "Orphanet:3471", "milliliter per kilogram": "UO:0000198", "material supplier": "EFO:0004443", "Polydactyly of an index finger, unilateral": "Orphanet:295152", "female athlete triad syndrome": "EFO:1001790", "Congenital onychodysplasia": "Orphanet:79144", "Enterococcus faecalis": "NCBITaxon:1351", "NG Capture-C": "EFO:0008827", "Drosophila": "NCBITaxon:7215", "microgametophyte vegetative cell {http": "PO:0020099", "Progressive myoclonic epilepsy": "Orphanet:98261", "Diaphyseal medullary stenosis - bone malignancy": "Orphanet:85182", "vascular disease": "EFO:0004264", "plant reproductive system structure": "EFO:0000998", "Partial trisomy/tetrasomy of chromosome 18": "Orphanet:262682", "hexaploid {http": "PATO:0001384", "N,N-dimethylformamide": "CHEBI:17741", "fruit size 50 to 70% stage {http": "PO:0025507", "type II hypersensitivity reaction disease": "EFO:0005809", "cutaneous mastocytosis": "EFO:1000886", "neurofibroma": "EFO:0000622", "MeDIP-seq": "EFO:0003749", "S wave amplitude": "EFO:0007740", "Alagille syndrome due to 20p12 microdeletion": "Orphanet:261600", "Autosomal recessive sideroblastic anemia": "Orphanet:260305", "Noonan syndrome-like disorder with loose anagen hair": "Orphanet:2701", "Hypogonadotropic hypogonadism associated with other endocrinopathies": "Orphanet:181390", "Conjunctival hemangioma or hemolymphangioma": "Orphanet:98612", "ND06229 {http": "CLO:0029036", "narcolepsy without cataplexy": "EFO:0005855", "A-549 cell": "BTO:0000018", "hyperthyroxinemia": "EFO:0004127", "Stiff skin syndrome": "Orphanet:2833", "Hypochondrogenesis": "Orphanet:93297", "cholangiocyte": "CL:1000488", "Hidrotic ectodermal dysplasia, Christianson-Fourie type": "Orphanet:1808", "mural granulosa cell": "EFO:0005289", "transcription profiling by array": "EFO:0002768", "cytotoxicity measurement": "EFO:0006952", "Leuconostoc mesenteroides": "NCBITaxon:1245", "Acid phosphatase deficiency": "Orphanet:35121", "Oculo-auriculo-vertebral spectrum": "Orphanet:141132", "Chronic diarrhea with villous atrophy": "Orphanet:1670", "maleate (-2) {http": "CHEBI:30780", "X-linked intellectual disability, Nascimento type": "Orphanet:163956", "NCI-H1155": "EFO:0002250", "Rapid-onset childhood obesity - hypothalamic dysfunction - hypoventilation - autonomic dysregulation syndrome": "Orphanet:293987", "oral lichen planus": "EFO:0008517", "Oculomotor apraxia or related oculomotor disease": "Orphanet:98688", "Hirsutism {http": "HP:0001007", "Combined oxidative phosphorylation defect type 4": "Orphanet:254925", "COASY protein-associated neurodegeneration": "Orphanet:397725", "Ring chromosome": "Orphanet:363203", "Paroxysmal Hemicrania": "EFO:1001822", "X-linked progressive cerebellar ataxia": "Orphanet:1175", "SKLMS1": "EFO:0002331", "lateral root meristem": "EFO:0001010", "information processing speed": "EFO:0004363", "Okihiro syndrome due to a point mutation": "Orphanet:261647", "otic lateral line neuromast": "UBERON:2000136", "Machado-Joseph disease type 2": "Orphanet:276241", "DNA synthesis inhibitor": "CHEBI:59517", "atrial natriuretic factor measurement": "EFO:0004789", "Leukoencephalopathy - dystonia - motor neuropathy": "Orphanet:163684", "RNA": "CHEBI:33697", "Rare pervasive developmental disorder": "Orphanet:168778", "dopaminergic antagonist": "CHEBI:48561", "adrenergic antagonist": "CHEBI:37887", "Microphthalmia - brain atrophy": "Orphanet:77299", "Deinococcus radiodurans R1": "NCBITaxon:243230", "phosphorus measurement": "EFO:0004861", "Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly": "Orphanet:93576", "SLC35A1-CDG": "Orphanet:238459", "Autosomal dominant hypophosphatemic rickets": "Orphanet:89937", "Syndromic visceral malformation": "Orphanet:108973", "serum albumin": "PR:000003918", "GM17154 {http": "CLO:0013961", "Partial deletion of chromosome 20": "Orphanet:261846", "Split foot": "Orphanet:294994", "CLN3 disease": "Orphanet:228346", "employment status": "EFO:0005241", "Brucella abortus": "NCBITaxon:235", "Fibrofolliculoma": "HP:0030436", "behavioral abnormality": "HP:0000708", "Isolated CoQ-cytochrome C reductase deficiency": "Orphanet:1460", "Schistosomiasis mansoni": "EFO:1001420", "hematopoietic stem cell": "CL:0000037", "RPL": "EFO:0008899", "ES2": "EFO:0002177", "U937": "EFO:0001257", "DLAF": "EFO:0008712", "asbestos exposure measurement": "EFO:0004806", "culture condition": "BTO:0000332", "presumptive ventral fin fold": "UBERON:2005103", "X-linked myopathy with postural muscle atrophy": "Orphanet:178461", "Minor Salivary Gland Adenocarcinoma": "EFO:1000379", "Hypertrichosis lanuginosa congenita": "Orphanet:2222", "stem cell": "CL:0000034", "reduced representation preparation": "EFO:0004178", "Tracheal neoplasm": "EFO:1001437", "spontaneous preterm birth": "EFO:0006917", "HCC1319": "EFO:0006425", "Multinodular goiter - cystic kidney - polydactyly": "Orphanet:2091", "Achenbach syndrome": "EFO:1000661", "Rare parkinsonian syndrome due to genetic neurodegenerative disease": "Orphanet:307055", "Channelopathy with epilepsy": "Orphanet:182083", "MUTZ-3": "EFO:0005395", "Superficial Fibromatosis": "EFO:1000556", "SW1990": "EFO:0002365", "Pisum sativum": "NCBITaxon:3888", "GA10": "EFO:0002181", "Rigid spine syndrome": "Orphanet:97244", "primary hypertension": "EFO:1002032", "Ovarioleukodystrophy": "Orphanet:99853", "non-small cell lung adenocarcinoma": "EFO:0005288", "infectious meningitis": "EFO:0000584", "microgram": "UO:0000023", "Primary bone dysplasia with defective bone mineralization": "Orphanet:93447", "GM17289 {http": "CLO:0013077", "Atrial septal defect, coronary sinus type": "Orphanet:99104", "Combined immunodeficiency T+ B+ due to partial RAG1 deficiency": "Orphanet:231154", "Gangliosidosis": "Orphanet:309144", "Peliosis Hepatis": "EFO:1001387", "Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm": "EFO:1000392", "Oculo-skeletal-renal syndrome": "Orphanet:2716", "Xenopus laevis": "NCBITaxon:8355", "Epidermal Inclusion Cyst": "EFO:1000243", "J774.2 cell": "BTO:0001030", "TraDIS sequencing": "EFO:0005219", "Columbia ecotype": "EFO:0005147", "Tuber melanosporum": "NCBITaxon:39416", "DoTc2": "EFO:0002171", "gibberellin A3": "CHEBI:28833", "GM14447 {http": "CLO:0031260", "Familial infantile myoclonic epilepsy": "Orphanet:352582", "Esophagitis": "HP:0100633", "Ehlers-Danlos syndrome": "Orphanet:98249", "EPLC-272H": "EFO:0006573", "Escherichia coli str. K-12 substr. MG1655": "NCBITaxon:511145", "Alagille syndrome": "Orphanet:52", "aristolochic acid": "CHEBI:2825", "Mitochondrial oxidative phosphorylation disorder": "Orphanet:223713", "twin design": "EFO:0001431", "embryonic foregut": "FBbt:00005606", "Paternal uniparental disomy of chromosome 5": "Orphanet:96190", "Radiation-induced nausea and vomiting": "EFO:0006912", "second": "UO:0000010", "acneiform dermatitis": "EFO:1000662", "diethylstilbestrol": "CHEBI:41922", "Ehlers-Danlos syndrome, progeroid type": "Orphanet:75496", "(S)-alpha-methyl-4-carboxyphenylglycine": "CHEBI:43876", "Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons": "Orphanet:401964", "GM18505": "EFO:0005332", "arachidonate {http": "CHEBI:32395", "Varicella Zoster infection": "EFO:0006509", "T84": "EFO:0002084", "salivary gland lesion": "EFO:0007124", "Autoimmune lymphoproliferative syndrome": "Orphanet:3261", "campylobacteriosis": "EFO:0007190", "I-YSL": "UBERON:2000712", "HPAM1": "EFO:0006280", "Idiopathic CD4 lymphocytopenia": "Orphanet:228000", "Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy": "Orphanet:1369", "Kleefstra syndrome due to a point mutation": "Orphanet:261652", "Hereditary arterial and articular multiple calcification syndrome": "Orphanet:289601", "NCI-H1092": "EFO:0002249", "Motor developmental delay due to 14q32.2 paternally expressed gene defect": "Orphanet:254516", "Drechslera sp.": "NCBITaxon:67606", "urinary uric acid to creatinine ratio": "EFO:0007935", "Amyotrophic lateral sclerosis type 4": "Orphanet:357043", "Keutel syndrome": "Orphanet:85202", "Susceptibility to respiratory infections associated with CD8alpha chain mutation": "Orphanet:169085", "embryonic stage 5": "EFO:0005864", "Thiopurine S-methyltransferase deficiency": "Orphanet:3315", "anterior spiracle specific anlage": "EFO:0000263", "M\u00c3\u00b6bius syndrome - axonal neuropathy - hypogonadotropic hypogonadism": "Orphanet:2560", "3-nitropropionic acid": "CHEBI:16348", "Adrenal Medullary Hyperplasia": "EFO:1000076", "lymphoma or leukaemia cell line": "EFO:0002937", "choroid plexus": "UBERON:0001886", "embryonic day 13": "EFO:0007642", "Distal Muscle weakness {http": "HP:0002460", "Vgamma1.1-positive, Vdelta6.3-positive thymocyte": "CL:0002412", "Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia": "Orphanet:2005", "Congenital isolated thyroxine-binding globulin deficiency": "Orphanet:209893", "CS57731": "EFO:0000077", "Sirenomelia": "Orphanet:3169", "acute myeloblastic leukemia without maturation": "EFO:0003027", "Intrahepatic cholestasis of pregnancy": "EFO:0009048", "embryonic day 12.5": "EFO:0002563", "GM18951": "EFO:0005349", "Autosomal dominant secondary polycythemia": "Orphanet:247511", "Distal monosomy 10p": "Orphanet:1580", "Peyer's patch macrophage": "CL:0000870", "Rubinstein-Taybi syndrome due to EP300 haploinsufficiency": "Orphanet:353284", "Hirschsprung disease - ganglioneuroblastoma": "Orphanet:2151", "vas deferens": "UBERON:0001000", "Salmonella Infections": "EFO:1001418", "pimelate(2-) {http": "CHEBI:36165", "CODAS syndrome": "Orphanet:1458", "Thyrocerebrorenal syndrome": "Orphanet:3327", "cocaine": "CHEBI:27958", "caudal tuberal nucleus": "UBERON:2000482", "Geospiza difficilis": "NCBITaxon:87173", "Familial hyperinsulinism": "Orphanet:276525", "Ma-Mel-11 cell": "BTO:0005339", "dipetalonemiasis": "EFO:0007237", "Lactobacillus rossiae": "NCBITaxon:231049", "DPM1-CDG": "Orphanet:79322", "lymphoid lineage restricted progenitor cell": "CL:0000838", "Autosomal dominant chondrodysplasia punctata": "Orphanet:79344", "suicide ideation measurement": "EFO:0007619", "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form": "Orphanet:315311", "Male hypergonadotropic hypogonadism - intellectual disability - skeletal anomalies": "Orphanet:2234", "Hyperinsulinism due to HNF1A deficiency": "Orphanet:324575", "CD38-negative IgG memory B cell": "CL:0002108", "dorsal pharyngeal muscle primordium": "FBbt:00005498", "Genetic multiple congenital anomalies/dysmorphic syndrome - variable intellectual disability": "Orphanet:330197", "dorsum": "UBERON:0001137", "CS57778": "EFO:0000115", "cleavage stage": "UBERON:0000107", "initial time point": "EFO:0004425", "GM17228 {http": "CLO:0014359", "renal leiomyoma": "EFO:1000050", "replicate design": "EFO:0001776", "secondary hyperparathyroidism": "EFO:1001173", "Disorder of beta and omega amino acid metabolism": "Orphanet:308407", "Partial duplication of chromosome 19": "Orphanet:262687", "NCI-H2461": "EFO:0006681", "anxiety disorder": "EFO:0006788", "sensory system disease": "EFO:0001058", "epidermal growth factor": "EFO:0003298", "Clostridium difficile": "NCBITaxon:1496", "small adipocyte": "EFO:0002573", "Leu-Gly {http": "CHEBI:74534", "preBCR-positive large pre-B-II cell": "CL:0000952", "bacterial meningitis": "EFO:1000831", "prostate specific antigen measurement": "EFO:0004624", "YCC6": "EFO:0002881", "lysozyme C measurement": "EFO:0008216", "2p15p16.1 microdeletion syndrome": "Orphanet:261349", "fear of pain measurement": "EFO:0008330", "Cucumber mosaic virus (strain FNY)": "NCBITaxon:12307", "psoriasis vulgaris": "EFO:1001494", "chondromyxoid fibroma": "EFO:0000332", "piperidin-2-one {http": "CHEBI:77761", "Hereditary gingival fibromatosis": "Orphanet:2024", "labeled specimen": "OBI:0000924", "Midline interhemispheric variant of holoprosencephaly": "Orphanet:93926", "Dermatofibrosarcoma protuberans": "Orphanet:31112", "leukocyte activation": "GO:0045321", "Farage": "EFO:0006393", "Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema": "Orphanet:69088", "CS57581": "EFO:0000021", "Lung Signet Ring Cell Carcinoma": "EFO:1000338", "Burkholderia pseudomallei K96243": "NCBITaxon:272560", "etoposide": "CHEBI:4911", "age of onset": "HP:0011007", "liver CD103-negative dendritic cell": "CL:0002505", "Testicular agenesis": "Orphanet:325124", "retinal cancer": "EFO:0005716", "glycosylation": "GO:0070085", "response to tamsulosin": "GO:1901905", "calcium/calmodulin-dependent protein kinase type 1D measurement": "EFO:0008063", "NALM1": "EFO:0002244", "Madelung deformity, unilateral": "Orphanet:295221", "response to aspirin": "GO:1903492", "Autosomal dominant Charcot-Marie-Tooth disease type 2E": "Orphanet:99939", "hydroxymalonate(1-) {http": "CHEBI:30844", "SeqZip": "EFO:0008920", "potassium chloride": "CHEBI:32588", "secretory granule membrane": "GO:0030667", "1,7-dimethylxanthine {http": "CHEBI:25858", "Gingival fibromatosis-hypertrichosis syndrome": "Orphanet:2026", "sampling time": "EFO:0000689", "deafness": "EFO:0001063", "flower meristem {http": "PO:0000229", "AG10941 {http": "CLO:0021459", "NOME-Seq": "EFO:0008830", "myxosarcoma": "EFO:1001056", "3,3',5-triiodo-L-thyronine": "CHEBI:18258", "invertebrate limb": "EFO:0000884", "Cone rod dystrophy": "Orphanet:1872", "polychromatophilic erythroblast": "CL:0000550", "protein C measurement": "EFO:0004633", "basophil progenitor cell": "CL:0000613", "somatic nervous system": "CL:0000111", "facial pigmentation measurement": "EFO:0006942", "rhegmatogenous retinal detachment": "EFO:0005240", "psychotic symptoms": "EFO:0005940", "GM17179 {http": "CLO:0014028", "conventional dendritic cell": "CL:0000990", "Schistosomiasis japonica": "EFO:1001419", "gondoic acid measurement": "EFO:0007975", "GM17115 {http": "CLO:0014952", "NCI-H1770": "EFO:0002265", "late pro-B cell": "CL:0002048", "BMI-adjusted waist circumference": "EFO:0007789", "Qualitative or quantitative defects of plectin": "Orphanet:209196", "Hyaluronidase deficiency": "Orphanet:67041", "Pseudopseudohypoparathyroidism": "Orphanet:79445", "SLBS": "EFO:0008928", "Clinodactyly {http": "HP:0030084", "Autosomal recessive limb-girdle muscular dystrophy type 2T": "Orphanet:363623", "Eastern equine encephalitis": "EFO:0007242", "interleukin-1 beta (Rattus norvegicus)": "EFO:0003796", "picomole": "UO:0000042", "Neurospora crassa": "NCBITaxon:5141", "embryo stage": "EFO:0007725", "CHP212": "EFO:0002133", "Penicillium islandicum": "NCBITaxon:28573", "array control buffer": "EFO:0005434", "progesterone receptor binding": "GO:0033142", "Non-Functional Pancreatic Neuroendocrine Tumor": "EFO:1000398", "day": "UO:0000033", "caerulein": "CHEBI:59219", "Hereditary sensory and autonomic neuropathy with spastic paraplegia": "Orphanet:139578", "compound treatment design": "EFO:0001755", "Distal monosomy 4q": "Orphanet:96145", "lipoprotein-associated phospholipase A(2) change measurement": "EFO:0008432", "Partial deletion of chromosome 5": "Orphanet:261786", "Syndromic craniosynostosis": "Orphanet:139393", "acute basophilic leukemia": "EFO:0003029", "phobic disorder": "EFO:1001908", "Larynx atresia": "Orphanet:1202", "Syndromic palpebral coloboma": "Orphanet:98566", "HEL": "EFO:0006579", "paroxetine": "CHEBI:7936", "Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency": "Orphanet:329314", "cimetidine": "CHEBI:3699", "Infantile epilepsy syndrome": "Orphanet:98258", "subacute sclerosing panencephalitis": "EFO:0007502", "CB30": "EFO:0004044", "1-stearoyl-2-arachidonoyl-sn-glycero-3-phosphocholine {http": "CHEBI:74965", "SW1353": "EFO:0002360", "Notophthalmus viridescens": "NCBITaxon:8316", "Phosphoenolpyruvate carboxykinase 2 deficiency": "Orphanet:79317", "enterocolitis": "EFO:1001481", "benign monoclonal gammopathy": "EFO:1000836", "Isolated autosomal dominant hypomagnesemia, Glaudemans type": "Orphanet:199326", "chronic pancreatitis": "EFO:0000342", "spindle organization": "GO:0007051", "GM17764 {http": "CLO:0016604", "Autosomal dominant optic atrophy and cataract": "Orphanet:67036", "CLIP-seq": "EFO:0003143", "Familial afibrinogenemia": "Orphanet:98880", "embryonic day 14.5": "EFO:0002565", "Occipital pachygyria and polymicrogyria": "Orphanet:280640", "Agrotis segetum": "NCBITaxon:47767", "granulocyte": "CL:0000094", "Anaplastic Large Cell Lymphoma, ALK-Negative": "EFO:1000083", "ventral thoracic disc": "UBERON:6001780", "Isolated congenital hypoglossia/aglossia": "Orphanet:141152", "hyperlipidemia": "EFO:0003774", "Candida glabrata": "NCBITaxon:5478", "Dilated cardiomyopathy with ataxia": "Orphanet:66634", "invasive ductal and lobular carcinoma": "EFO:0000552", "lateral medullary syndrome": "EFO:1001011", "Prata-Liberal-Goncalves syndrome": "Orphanet:2956", "Globodera pallida": "NCBITaxon:36090", "iPS-18a": "EFO:0007105", "Buschke-Ollendorff syndrome": "Orphanet:1306", "axial length measurement": "EFO:0005318", "Postpartum Thyroiditis": "EFO:1001403", "MM.1S": "EFO:0005724", "Autosomal dominant hereditary axonal motor and sensory neuropathy": "Orphanet:140456", "purine nucleoside triphosphate metabolic process": "GO:0009144", "response to virus": "GO:0009615", "SARS coronavirus Tor2": "NCBITaxon:227984", "Pili bifurcati": "Orphanet:720", "Primary dystonia, DYT2 type": "Orphanet:99657", "Autosomal recessive intermediate Charcot-Marie-Tooth disease type B": "Orphanet:254334", "Ovarian Endometrioid Adenocarcinoma with Squamous Differentiation": "EFO:1000417", "GM17807 {http": "CLO:0016503", "Craniofacial conodysplasia": "Orphanet:85168", "Amish lethal microcephaly": "Orphanet:99742", "macromolecule glycosylation": "GO:0043413", "Bj\u00c3\u00b6rnstad syndrome": "Orphanet:123", "Autosomal recessive non-syndromic sensorineural deafness type DFNB": "Orphanet:90636", "Fusarium incarnatum": "NCBITaxon:298378", "rhombomere 8": "UBERON:0005527", "myoepithelial cell": "CL:0000185", "HIV enteropathy": "EFO:0007311", "Coxopodopatellar syndrome": "Orphanet:1509", "Congenital primary megaureter, obstructed form": "Orphanet:238646", "Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus": "Orphanet:83473", "urinary schistosomiasis": "EFO:0007530", "mitochondrial envelope": "GO:0005740", "NCI-H1703": "EFO:0002264", "Intellectual disability-developmental delay-contractures syndrome": "Orphanet:3454", "Cal-0": "EFO:0005165", "chronic obstructive pulmonary disease": "EFO:0000341", "3-hydroxy-3-methylglutaryl-CoA synthase deficiency": "Orphanet:35701", "sodium nitroprusside": "CHEBI:29321", "Leydig cell": "CL:0000178", "Complement component 3 deficiency": "Orphanet:280133", "Malignant atrophic papulosis": "Orphanet:679", "Ferro-cerebro-cutaneous syndrome": "Orphanet:397922", "definitive endoderm": "UBERON:0005439", "neonatal systemic lupus erthematosus": "EFO:0004537", "acute retinal necrosis syndrome": "EFO:1000795", "interleukin 2 measurement": "EFO:0008331", "Autosomal dominant intermediate Charcot-Marie-Tooth disease": "Orphanet:90114", "posterior lateral line system": "UBERON:2001471", "3q29 microdeletion syndrome": "Orphanet:65286", "Autosomal recessive spastic paraplegia type 54": "Orphanet:320380", "part per billion": "UO:0000170", "Caucasian": "EFO:0003156", "mass percent": "UO:0000163", "blood cadmium measurement": "EFO:0007576", "pancreas primordium": "UBERON:0003921", "Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification": "Orphanet:93358", "WM793": "EFO:0002873", "B220-low CD38-positive IgG-negative class switched memory B cell": "CL:0002123", "Juvenile Myelomonocytic Leukemia": "EFO:1000309", "RR interval": "EFO:0004831", "Central polydactyly of toes": "Orphanet:295010", "Common Hematopoietic Neoplasm": "EFO:1000201", "substance withdrawal syndrome": "EFO:0005800", "cubic centimeter": "UO:0000097", "Maylandia": "NCBITaxon:143623", "Congenital plasminogen activator inhibitor type 1 deficiency": "Orphanet:465", "coronary artery calcification": "EFO:0004723", "CD4-positive, alpha-beta cytotoxic T cell": "CL:0000934", "Congenital factor V deficiency": "Orphanet:326", "prolonged QT interval": "HP:0001657", "C1R cell": "BTO:0003699", "sigmoid colon": "UBERON:0001159", "measurement": "EFO:0001444", "Hemolytic anemia due to glutathione reductase deficiency": "Orphanet:90030", "ciprofloxacin": "CHEBI:100241", "Alpha delta granule deficiency": "Orphanet:734", "Postaxial tetramelic oligodactyly": "Orphanet:2730", "Eukaryota": "NCBITaxon:2759", "Phanerochaete chrysosporium": "NCBITaxon:5306", "energy intake": "EFO:0003939", "Agrobacterium tumefaciens str. C58": "NCBITaxon:176299", "ependymoma": "EFO:1000028", "photosensitivity disease": "EFO:1000752", "nasopharyngeal squamous cell carcinoma": "EFO:1000058", "HMT3522S1": "EFO:0001191", "Xeroderma pigmentosum complementation group F": "Orphanet:276264", "Capture-C": "EFO:0007691", "response to irinotecan": "EFO:0004829", "Mitochondrial trifunctional protein deficiency": "Orphanet:746", "Mevalonate kinase deficiency": "Orphanet:309025", "Thoracomelic dysplasia": "Orphanet:1803", "Bilateral renal agenesis": "Orphanet:1848", "Hydrocephaly - tall stature - joint laxity": "Orphanet:2181", "FEV/FEC ratio": "EFO:0004713", "Pseudomonas syringae pv. tomato {has_synonym_type=\"equivalent_name\"}": "NCBITaxon:323", "Roch-Leri mesosomatous lipomatosis": "Orphanet:529", "immature Vgamma1.1-positive, Vdelta6.3-negative thymocyte": "CL:0002414", "Claviceps purpurea": "NCBITaxon:5111", "Emiliania huxleyi": "NCBITaxon:2903", "gangrene": "EFO:0008574", "Normal Breast-Like Subtype of Breast Carcinoma": "EFO:1000402", "Essential iris atrophy": "Orphanet:98981", "phosphorus metabolic process": "GO:0006793", "vitamin E measurement": "EFO:0004867", "Congenital factor XII deficiency": "Orphanet:330", "rectum": "UBERON:0001052", "Berardinelli-Seip congenital lipodystrophy": "Orphanet:528", "metformin": "CHEBI:6801", "pulmonary sarcoidosis": "DOID:13406", "Ring chromosome 8": "Orphanet:1450", "Trypanosoma brucei TREU927": "NCBITaxon:185431", "DNA repair defect other than combined T-cell and B-cell immunodeficiencies": "Orphanet:169346", "carbohydrate derivative metabolic process": "GO:1901135", "acute-on-chronic liver failure": "EFO:0007949", "Kit-positive, CD34-negative megakaryocyte erythroid progenitor cell": "CL:0002006", "miliary tuberculosis": "EFO:0007368", "body weight": "EFO:0004338", "Lewy body measurement": "EFO:0007021", "ATC Code N Nervous system": "EFO:0005643", "Distal trisomy 19q": "Orphanet:1717", "Anaplasma phagocytophilum HZ": "NCBITaxon:212042", "macromolecule modification": "GO:0043412", "Mucopolysaccharidosis type 6": "Orphanet:583", "Chylothorax": "EFO:1001780", "loneliness measurement": "EFO:0007865", "hemangioma": "EFO:1000635", "NCI-H2107": "EFO:0002278", "cartilage": "EFO:0000949", "Flat Urothelial Hyperplasia": "EFO:1000259", "intermediate cell mass of mesoderm": "UBERON:2000033", "contact dermatitis": "EFO:0005319", "EC-seq": "EFO:0008728", "EFM-192A": "EFO:0006568", "CNV-Seq": "EFO:0008695", "molecular quality": "PATO:0002182", "Congenital vertical talus": "Orphanet:178382", "Digital RNA": "EFO:0008710", "Neisseria meningitidis MC58": "NCBITaxon:122586", "Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome": "Orphanet:397744", "X-linked cerebellar ataxia": "Orphanet:247765", "head and neck squamous cell carcinoma": "EFO:0000181", "gefitinib": "CHEBI:49668", "MKN74": "EFO:0002834", "C57BL/6NJ": "EFO:0007732", "Swiss22": "EFO:0006299", "regulation of biological process": "GO:0050789", "Panhypopituitarism": "Orphanet:90695", "sedative drug": "CHEBI:35717", "globus pallidus": "UBERON:0001875", "response to anticonvulsant": "GO:0036277", "NCI-H2196": "EFO:0006676", "Intermittent maple syrup urine disease": "Orphanet:268173", "Vibrio vulnificus": "NCBITaxon:672", "response to bleomycin": "EFO:0007592", "microscopic colitis": "EFO:1001295", "CAP-seq": "EFO:0008671", "Polyostotic fibrous dysplasia": "Orphanet:93276", "OVCAR8": "EFO:0005444", "Hidrotic ectodermal dysplasia": "Orphanet:189", "Benign paroxysmal tonic upgaze of childhood with ataxia": "Orphanet:1179", "BK polyomavirus": "NCBITaxon:10629", "natural T-regulatory cell": "CL:0000903", "Genetic developmental defect of the eye": "Orphanet:183557", "Renal cysts and diabetes syndrome": "Orphanet:93111", "Arthroderma cajetani": "NCBITaxon:81846", "Exostoses - anetodermia - brachydactyly type E": "Orphanet:1962", "Giant Cell Tumor of Soft Tissue": "EFO:1000281", "SKM-1": "EFO:0006753", "Lepeophtheirus salmonis": "NCBITaxon:72036", "Peyer's patch": "UBERON:0001211", "Progressive osseous heteroplasia": "Orphanet:2762", "Glycogen storage disease due to muscle phosphorylase kinase deficiency": "Orphanet:715", "Familial cervical artery dissections": "Orphanet:36382", "chronic bronchitis": "EFO:0006505", "environmental history": "EFO:0004444", "Galactokinase deficiency": "Orphanet:79237", "plantaris": "UBERON:0011905", "Malignant Urinary System Neoplasm": "EFO:1000363", "Disorder of creatine biosynthesis": "Orphanet:79172", "Distal hereditary motor neuropathy type 1": "Orphanet:139518", "coronary stenosis": "EFO:1000882", "Macaca mulatta": "NCBITaxon:9544", "variant Creutzfeldt-Jakob disease": "EFO:1001233", "urea {http": "CHEBI:16199", "Autosomal recessive optic atrophy": "Orphanet:98675", "CB4855": "EFO:0004054", "DND-41": "EFO:0007074", "PRO-seq": "EFO:0008869", "Bladder exstrophy": "Orphanet:93930", "creatine kinase measurement": "EFO:0004534", "Late infantile CACH syndrome": "Orphanet:157716", "neurobehavioral manifestations": "EFO:0004364", "C4BP measurement": "EFO:0004572", "LIANTI": "EFO:0008785", "Partial deletion of the long arm of chromosome 6": "Orphanet:262047", "kainic acid": "CHEBI:31746", "agnosia": "EFO:0007136", "relapsing polychondritis": "EFO:1001148", "Autosomal recessive spastic paraplegia type 43": "Orphanet:320370", "Autosomal dominant dopa-responsive dystonia": "Orphanet:98808", "organ development": "GO:0048513", "Komagataella pastoris": "NCBITaxon:4922", "Abnormality of adipose tissue": "HP:0009124", "Primary megaureter, adult-onset form": "Orphanet:238642", "Spastic paraplegia - facial-cutaneous lesions": "Orphanet:2819", "microgram per square centimeter": "EFO:0004370", "RNET-seq": "EFO:0008898", "GM12865": "EFO:0005338", "Microcephaly - intellectual disability - phalangeal and neurological anomalies": "Orphanet:137658", "Pendred syndrome": "Orphanet:705", "ND03432 {http": "CLO:0012496", "Hereditary central diabetes insipidus": "Orphanet:30925", "Adactyly of foot, bilateral": "Orphanet:295118", "testicular seminoma": "EFO:0003101", "control": "EFO:0001461", "Mobius syndrome": "EFO:1001046", "thymus": "UBERON:0002370", "proteomic profiling": "EFO:0000746", "Cimex lectularius": "NCBITaxon:79782", "Aggregatibacter actinomycetemcomitans HK1651": "NCBITaxon:272556", "NCI-H661": "EFO:0002299", "1205-Lu": "EFO:0002810", "2,4-dichlorophenol": "CHEBI:16738", "Thymoma Type B3": "EFO:1000583", "Leptomyelolipoma": "Orphanet:268838", "2-hydroxyadipate(2-) {http": "CHEBI:57987", "material supplier role": "OBI:0000018", "Actinobacillus pleuropneumoniae": "NCBITaxon:715", "xylose": "CHEBI:18222", "borna disease": "EFO:0007178", "GM12264 {http": "CLO:0019004", "hypotension": "EFO:0005251", "Autosomal recessive Alport syndrome": "Orphanet:88919", "Heart defect - round face - congenital developmental delay": "Orphanet:1355", "Salmonella enterica subsp. enterica serovar Saintpaul": "NCBITaxon:90105", "SUDHL10": "EFO:0002354", "Palmoplantar keratoderma-spastic paralysis syndrome": "Orphanet:2201", "Qualitative or quantitative defects of dysferlin": "Orphanet:207073", "GM17817 {http": "CLO:0016510", "hermaphrodite gonad": "UBERON:0002537", "Maxillonasal dysplasia": "Orphanet:1248", "clone by clone sequencing": "EFO:0003742", "radicicol": "CHEBI:556075", "IgG-negative class switched memory B cell": "CL:0002117", "diterpene": "CHEBI:35190", "delayed encephalopathy after acute carbon monoxide poisoning": "EFO:0005534", "GM17199 {http": "CLO:0013826", "GM12872": "EFO:0001159", "cytoskeletal part": "GO:0044430", "Nicotiana benthamiana": "NCBITaxon:4100", "Marshall-Smith syndrome": "Orphanet:561", "Microbrachycephaly - ptosis - cleft lip": "Orphanet:2511", "Mediastinal Malignant Germ Cell Tumor": "EFO:1000366", "Drosophila component": "EFO:0003334", "Myoclonus - cerebellar ataxia - deafness": "Orphanet:2589", "conjunctiva": "UBERON:0001811", "NCI-H1437": "EFO:0002254", "Skeletal dysplasia": "HP:0002652", "HCC1011": "EFO:0006422", "Cataract with Y-shaped suture opacities": "Orphanet:98985", "ajmaline": "CHEBI:28462", "CD16-positive myeloid dendritic cell": "CL:0002532", "vitamin A metabolic process": "GO:0006776", "Culex quinquefasciatus": "NCBITaxon:7176", "ACTH Syndrome, Ectopic": "EFO:1001256", "Combined T and B cell immunodeficiency": "Orphanet:101972", "Autosomal recessive bestrophinopathy": "Orphanet:139455", "response to olanzapine": "GO:0097333", "somatosensory cortex": "UBERON:0008930", "ILSXISS117/TejJ": "EFO:0003010", "Nephroblastoma": "Orphanet:654", "ML-DmD17-c3": "EFO:0005826", "IR (lox/lox)": "EFO:0002746", "GCS1-CDG": "Orphanet:79330", "Endometrial Hyperplasia without Atypia": "EFO:1000234", "orbital myositis": "EFO:1001819", "Ehlers-Danlos syndrome, periodontitis type": "Orphanet:75392", "Atrophic Vaginitis": "EFO:1001271", "Helicoverpa armigera": "NCBITaxon:29058", "Spermophilus tridecemlineatus": "NCBITaxon:43179", "cytotoxic T cell": "CL:0000910", "Radio-ulnar synostosis, unilateral": "Orphanet:295217", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D": "Orphanet:100046", "osteoarthritis, hand": "EFO:1000789", "Partial deletion of the long arm of chromosome 19": "Orphanet:262155", "Aspergillus fumigatus": "NCBITaxon:746128", "Hereditary late-onset Parkinson disease": "Orphanet:411602", "femtogram": "UO:0000026", "6-deoxycathasterone": "CHEBI:20714", "GM17800 {http": "CLO:0016491", "Bleeding diathesis due to thromboxane synthesis deficiency": "Orphanet:220443", "sudden cardiac arrest": "EFO:0004278", "Hyperkeratosis lenticularis perstans": "Orphanet:409", "CS57884": "EFO:0000157", "CS57826": "EFO:0000134", "Conjunctival Disorder": "EFO:1000203", "Illumina HiSeq 2500": "EFO:0008565", "water bath": "OBI:0400155", "Salmonella enterica subsp. enterica serovar Newport": "NCBITaxon:108619", "respiratory aspiration": "EFO:1001839", "CS57812": "EFO:0000126", "X-linked spinocerebellar ataxia type 4": "Orphanet:85292", "X-linked intellectual disability, Wittwer type": "Orphanet:85291", "interdigitating dendritic cell sarcoma": "EFO:0007329", "Spinocerebellar ataxia type 15/16": "Orphanet:98769", "N-acetylisoleucine {http": "CHEBI:84056", "Spinacia oleracea": "NCBITaxon:3562", "Maternal uniparental disomy of chromosome 14": "Orphanet:96184", "Reoviridae infectious disease": "EFO:0007464", "1-tetradecanoyl-2-[(9Z,12Z)-octadecadienoyl]-sn-glycero-3-phosphocholine {http": "CHEBI:86094", "Colorectal Neuroendocrine Tumor G1": "EFO:1000195", "Hereditary neuropathy with liability to pressure palsies": "Orphanet:640", "Bergmann glial cell": "CL:0000644", "apoptotic amnioserosa": "FBbt:00005556", "Disorder of ornithine metabolism": "Orphanet:289869", "Familial hemophagocytic lymphohistiocytosis": "Orphanet:540", "Parotid Gland Adenoid Cystic Carcinoma": "EFO:1000459", "epihyal": "UBERON:2000627", "Synechococcus phage S-IO17": "NCBITaxon:375050", "Mytilus galloprovincialis": "NCBITaxon:29158", "GM17223 {http": "CLO:0014367", "A2058": "EFO:0006361", "LDH-related sciatica symptom severity measurement": "EFO:0007941", "sarcosine {http": "CHEBI:15611", "crypt": "BTO:0000305", "HCC366": "EFO:0003131", "risk-taking behaviour": "EFO:0008579", "Congenital primary megaureter, refluxing form": "Orphanet:238650", "alloxanthine {http": "CHEBI:28315", "Orthomyxoviridae infectious disease": "EFO:0007411", "S3": "EFO:0005838", "Long chain acyl-CoA dehydrogenase deficiency": "Orphanet:99900", "Hyperalphalipoproteinemia": "Orphanet:181428", "branchial muscle": "UBERON:0000933", "carotid plaque build": "EFO:0006501", "Subependymal nodular heterotopia": "Orphanet:101030", "plasma cell leukemia": "EFO:0006475", "Oculoosteocutaneous syndrome": "Orphanet:2713", "protoplast": "CL:0000371", "epithelial cell derived cell line": "EFO:0001641", "islet of Langerhans": "UBERON:0000006", "neoplasm of mature B-cells": "EFO:0000096", "abnormality of the nose": "HP:0000366", "squamous papilloma": "EFO:1001970", "HSV2 virologic severity measurement": "EFO:0009010", "interneuron": "CL:0000099", "Partial monosomy of the long arm of chromosome 10": "Orphanet:262083", "pulmonary aspergillosis": "EFO:1001834", "2-hydroxyisobutyrate {http": "CHEBI:19641", "Bacillus anthracis str. Sterne": "NCBITaxon:260799", "androgen": "CHEBI:50113", "SNU5": "EFO:0002351", "Alstr\u00c3\u00b6m syndrome": "Orphanet:64", "substantia propria of cornea {http": "UBERON:0001777", "H4": "EFO:0002184", "paneth cell": "CL:0000510", "N-glycan measurement": "EFO:0004999", "SNU-601": "EFO:0006756", "Porphyria cutanea tarda": "Orphanet:101330", "GM17150 {http": "CLO:0013956", "material sample": "OBI:0000747", "Gossypium herbaceum": "NCBITaxon:34274", "Congenital muscular dystrophy with hyperlaxity": "Orphanet:371007", "collection longitude": "EFO:0005021", "Autosomal recessive hyperinsulinism due to SUR1 deficiency": "Orphanet:79643", "central nervous system cancer": "EFO:0000326", "Infantile Bartter syndrome with sensorineural deafness": "Orphanet:89938", "Spasticity - intellectual disability - X-linked epilepsy": "Orphanet:3175", "alive": "PATO:0001421", "Bird headed-dwarfism, Montreal type": "Orphanet:2617", "cathepsin S measurement": "EFO:0008073", "Sulfolobus acidocaldarius": "NCBITaxon:2285", "dichloromethane": "CHEBI:15767", "Hereditary angioedema": "Orphanet:91378", "Rhizobium etli CFN 42": "NCBITaxon:347834", "Functional neutrophil defect": "Orphanet:183681", "Epilepsy - microcephaly - skeletal dysplasia": "Orphanet:1948", "Autosomal recessive spastic paraplegia type 58": "Orphanet:397946", "uterine leiomyosarcoma cell line": "BTO:0002488", "axilla": "UBERON:0009472", "West syndrome": "Orphanet:3451", "nucleus of medial longitudinal fasciculus of medulla": "UBERON:2000815", "endometrial carcinoma": "EFO:1001512", "pemphigus vulgaris": "EFO:0004719", "intestinal bulb": "UBERON:2001076", "phospholipase A2 inhibitor": "CHEBI:50469", "parapsoriasis": "EFO:1000747", "Short stature - valvular heart disease - characteristic facies": "Orphanet:2868", "Nuclear cataract": "Orphanet:98991", "response to escitalopram": "EFO:0007871", "pseudomembranous enterocolitis": "EFO:1001314", "X-linked parkinsonism-spasticity syndrome": "Orphanet:363654", "MEC2": "EFO:0006285", "NCI-H1334": "EFO:0003117", "selenium measurement": "EFO:0006331", "Brain malformation - congenital heart disease - postaxial polydactyly": "Orphanet:75389", "N-acetyl-L-aspartate(2-) {http": "CHEBI:16953", "response to heat": "GO:0009408", "timepoint": "EFO:0000724", "EFM-192C": "EFO:0006570", "cisplatin": "CHEBI:27899", "sodium selenite": "CHEBI:48843", "IgG sialylation measurement": "EFO:0008428", "GM17102 {http": "CLO:0014896", "tibialis anterior": "UBERON:0001385", "Enterococcus faecium": "NCBITaxon:1352", "vulvar inverted follicular keratosis": "EFO:1000778", "Carey-Fineman-Ziter  syndrome": "Orphanet:1358", "nanomole": "UO:0000041", "actinobacillosis": "EFO:0007127", "Parkinsonim due to ATP13A2 deficiency": "Orphanet:314632", "5T33MM": "EFO:0006530", "Microsporum ferrugineum": "NCBITaxon:77205", "experiment performer": "EFO:0000647", "pregnenolone 16alpha-carbonitrile": "CHEBI:35591", "CS57750": "EFO:0000085", "prostate cancer cell line": "BTO:0001033", "GM17260 {http": "CLO:0013182", "amino acid": "CHEBI:33709", "embryonic inner optic lobe primordium": "FBbt:00000461", "MethylCap-Seq": "EFO:0008805", "Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism": "Orphanet:100034", "Illumina HiSeq 1000 standard manufacturer's protocol": "EFO:0005085", "late gestational weight gain": "EFO:0008436", "Blue diaper syndrome": "Orphanet:94086", "neural crest cell": "CL:0000333", "picogram per milliliter": "EFO:0004385", "YAPC": "EFO:0006778", "Aspergillus oryzae": "NCBITaxon:5062", "5-amino-1-(5-phospho-D-ribosyl)imidazole": "CHEBI:28843", "hypopharynx": "UBERON:0001051", "embryonal neoplasm": "EFO:0005784", "cis/trans-18": "EFO:0006824", "X-linked intellectual disability - epilepsy": "Orphanet:2076", "iPS-27b": "EFO:0007109", "1-oleoyl-sn-glycero-3-phosphoethanolamine {http": "CHEBI:75168", "mature CD8_alpha-positive CD11b-negative dendritic cell": "CL:0001005", "Lentivirus Infections": "EFO:1001357", "class switched memory B cell": "CL:0000972", "Benign Ovarian Surface Epithelial-Stromal Tumor": "EFO:1000117", "Astatotilapia": "NCBITaxon:8152", "miliaria rubra": "EFO:1000735", "Pneumovirus Infections": "EFO:1001401", "Ophthalmomandibulomelic dysplasia": "Orphanet:2741", "Harrod syndrome": "Orphanet:2115", "dermis": "UBERON:0002067", "Wolfram-like syndrome": "EFO:0009063", "Spondylometaphyseal dysplasia": "Orphanet:254", "COV413A": "EFO:0006557", "response to cytosine arabinoside": "EFO:0005655", "Short-limb skeletal dysplasia with severe combined immunodeficiency": "Orphanet:935", "Atrial septal defect, ostium secundum type": "Orphanet:99103", "Hyperinsulinism due to glucokinase deficiency": "Orphanet:79299", "Acrofacial dysostosis": "Orphanet:364574", "histiocytoma": "EFO:0005561", "Autosomal recessive spastic paraplegia type 61": "Orphanet:401780", "vagal ganglion 3": "UBERON:2001304", "Dermatopathia pigmentosa reticularis": "Orphanet:86920", "Aortic arch anomaly - peculiar facies - intellectual disability": "Orphanet:1110", "gastrula bud": "EFO:0001294", "cognitive impairment": "HP:0100543", "left ventricular systolic function measurement": "EFO:0008206", "CS8581": "EFO:0000167", "Short nose {http": "HP:0003196", "Qualitative or quantitative defects of alpha-sarcoglycan": "Orphanet:207060", "Charcot-Marie-Tooth disease type 2H": "Orphanet:101102", "gland": "UBERON:0002530", "Lymphoplasmacyte-Rich Meningioma": "EFO:1000342", "enucleated reticulocyte": "CL:0002422", "colonic neoplasm": "EFO:0004288", "C9orf72 mutation status": "EFO:0008352", "1-[2-(benzhydryloxy)ethyl]-4-(3-phenylpropyl)piperazine dihydrochloride": "CHEBI:64091", "Becker muscular dystrophy": "Orphanet:98895", "segmentation 26+ somites": "EFO:0001321", "Congenital sucrase-isomaltase deficiency": "Orphanet:35122", "bacterial sexually transmitted disease": "EFO:0003955", "Hypomesus transpacificus": "NCBITaxon:137520", "X-linked non-syndromic intellectual disability": "Orphanet:777", "Intellectual disability, Buenos-Aires type": "Orphanet:3079", "ejaculatory duct": "UBERON:0000999", "PLA2G6-associated neurodegeneration": "Orphanet:329303", "Sotos syndrome": "Orphanet:821", "Radial deficiency - tibial hypoplasia": "Orphanet:1121", "Ankyloblepharon - ectodermal defects - cleft lip/palate": "Orphanet:1071", "coronary thrombosis": "EFO:1000883", "Familial thoracic aortic aneurysm and aortic dissection": "Orphanet:91387", "focal epithelial hyperplasia": "EFO:0007275", "apolipoprotein A-IV measurement": "EFO:0007848", "beta-2 microglobulin measurement": "EFO:0005197", "osteoclast": "CL:0000092", "parametritis": "EFO:1001084", "OCI-M2": "EFO:0006713", "Elodea nuttallii": "NCBITaxon:55313", "acute lymphoblastic leukemia": "EFO:0000220", "Lysosomal acid lipase deficiency": "Orphanet:275761", "mature Vgamma2-positive fetal thymocyte": "CL:0002403", "Familial chondromalacia patellae": "Orphanet:1428", "Autosomal recessive chorioretinopathy-microcephaly": "Orphanet:2518", "Ehlers-Danlos syndrome type 7B": "Orphanet:99876", "rapid kidney function decline": "EFO:0006836", "Polydactyly-myopia syndrome": "Orphanet:2917", "neuropathy, hereditary motor and sensory, type vib": "EFO:0009075", "Familial clubfoot due to PITX1 point mutation": "Orphanet:293150", "2q24 microdeletion syndrome": "Orphanet:1617", "Obesity due to pro-opiomelanocortin deficiency": "Orphanet:71526", "Costello syndrome": "Orphanet:3071", "Aspergillus niger": "NCBITaxon:5061", "maxillary sensory complex primordium": "FBbt:00005544", "estradiol": "CHEBI:23965", "anti-CD3": "EFO:0003317", "Osteoporosis - pseudoglioma": "Orphanet:2788", "Hypotrichosis-intellectual disability, Lopes type": "Orphanet:2266", "larval day 7-13": "EFO:0001309", "Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome": "Orphanet:65282", "Sneddon syndrome": "EFO:1001186", "picomole per microliter": "EFO:0005313", "Palpebral malignant melanoma": "Orphanet:98589", "Malpighian tubule": "UBERON:0001054", "T3 tumor stage": "EFO:0004940", "phagocyte bactericidal dysfunction": "EFO:0007433", "whole plant fruit formation stage 30 to 50% {http": "PO:0007029", "clinically amyopathic dermatomyositis": "EFO:0008532", "Syndromic X-linked ichthyosis": "Orphanet:281090", "lymphoid MHC-II-negative non-classical monocyte": "CL:0002475", "sampling site": "EFO:0000688", "anterior lateral mesoderm": "UBERON:2005039", "M\u00c3\u00bcllerian derivatives - lymphangiectasia - polydactyly": "Orphanet:1655", "Borderline Ovarian Surface Epithelial-Stromal Tumor": "EFO:1000140", "Cyclamen persicum": "NCBITaxon:87530", "contact dermatitis due to nickel": "EFO:0005320", "Thrombocytopenia - Robin sequence": "Orphanet:3323", "caspase-3 measurement": "EFO:0008070", "adult B acute lymphoblastic leukemia": "EFO:1001935", "pulmonary valve stenosis": "EFO:1001138", "KYSE-520": "EFO:0006632", "HUVEC cell": "EFO:0002451", "mammary gland cell line": "EFO:0002884", "potassium bromide": "CHEBI:32030", "Punctate palmoplantar keratoderma type 2": "Orphanet:79502", "GM14479 {http": "CLO:0031535", "15q24 microdeletion syndrome": "Orphanet:94065", "Dehydratase deficiency": "Orphanet:1578", "Familial symmetric lipomatosis": "Orphanet:2398", "Familial expansile osteolysis": "Orphanet:85195", "body height at birth": "EFO:0006784", "Adenylosuccinate lyase deficiency": "Orphanet:46", "sciatic neuropathy": "EFO:1001166", "Kit-low, CD34-positive eosinophil progenitor cell": "CL:0002007", "circular visceral muscle fibers": "FBbt:00005072", "Hereditary leiomyomatosis and renal cell cancer": "Orphanet:523", "embryonic blood": "BTO:0000381", "Theileria parva": "NCBITaxon:5875", "Glycogen storage disease due to glucose-6-phosphatase deficiency type a": "Orphanet:79258", "COPRO-seq": "EFO:0008696", "nucleus": "GO:0005634", "Rare genetic renal disease": "Orphanet:98056", "Autoimmune Hepatitis": "EFO:0005676", "GM17818 {http": "CLO:0016511", "metabolic rate measurement": "EFO:0005115", "retinol measurement": "EFO:0007900", "COV318": "EFO:0006382", "Nemaline myopathy": "Orphanet:607", "papaverine": "CHEBI:28241", "cannabinoid": "CHEBI:67194", "Metaphyseal chondrodysplasia, Spahr type": "Orphanet:2501", "microgram per liter": "UO:0000301", "myeloid leukemia cell line": "BTO:0000740", "chewing tobacco behavior": "EFO:0004774", "Mitral valve prolapse": "HP:0001634", "nanogram": "UO:0000024", "neuromedin U": "EFO:0003266", "ozone": "CHEBI:25812", "manic or hypomanic episode": "EFO:0007706", "Fibroblastic Neoplasm": "EFO:1000255", "Dehalococcoides sp. VS": "NCBITaxon:311424", "Dendritic keratitis": "EFO:1001883", "Abnormal glucose homeostasis": "HP:0011014", "atrioventricular node": "UBERON:0002352", "Parotid Gland Acinic Cell Carcinoma": "EFO:1000458", "Populus euphratica": "NCBITaxon:75702", "clinical treatment protocol": "EFO:0000355", "Kit and Sca1-positive hematopoietic stem cell": "CL:0001008", "GM12868": "EFO:0005341", "brassinazole": "CHEBI:73177", "GM17813 {http": "CLO:0016507", "Guanidinoacetate methyltransferase deficiency": "Orphanet:382", "Ichthyosis-short stature-brachydactyly-microspherophakia syndrome": "Orphanet:363992", "vasodilator agent": "CHEBI:35620", "refractive error measurement": "EFO:0007814", "Dyssegmental dysplasia, Rolland-Desbuquois type": "Orphanet:156731", "Male infertility with teratozoospermia due to single gene mutation": "Orphanet:399808", "histamine antagonist": "CHEBI:37956", "MIRA": "EFO:0008816", "Penicillium expansum": "NCBITaxon:27334", "anterior silk gland": "BTO:0001795", "Ulnar hemimelia, unilateral": "Orphanet:295075", "Sporadic idiopathic steroid-resistant nephrotic syndrome": "Orphanet:84271", "hypersensitivity": "GO:0002524", "late-onset Alzheimers disease": "EFO:1001870", "pentachloronitrobenzene": "CHEBI:34908", "Maternal 14q32.2 hypermethylation syndrome": "Orphanet:254534", "Paraplegia - brachydactyly - cone-shaped epiphysis": "Orphanet:2823", "COLO357": "EFO:0002710", "O-decanoyl-L-carnitine {http": "CHEBI:28717", "AA86": "EFO:0004025", "non-compaction cardiomyopathy": "EFO:0004686", "HPL1B": "EFO:0002705", "Zea mays": "NCBITaxon:4577", "Rare female infertility due to adrenal disorder of genetic origin": "Orphanet:400018", "tarsal region": "UBERON:0004454", "third instar larva stage": "EFO:0002682", "oxyphilic adenoma": "EFO:1001079", "GM14381 {http": "CLO:0031189", "vital signs": "EFO:0004303", "Mitochondrial myopathy - lactic acidosis - deafness": "Orphanet:2597", "EVSA-T": "EFO:0006574", "IGFBP-3 measurement": "EFO:0004626", "Beckwith-Wiedemann syndrome": "Orphanet:116", "Progressive sensorineural hearing impairment {http": "HP:0000408", "glycerophospholipid measurement": "EFO:0007630", "Genetic cardiac anomaly": "Orphanet:271853", "2P-Seq": "EFO:0008639", "Hemoglobin SC Disease": "EFO:1001797", "CB120": "EFO:0004074", "NADPH--cytochrome P450 reductase measurement": "EFO:0008242", "Niemann-Pick disease type C, late infantile neurologic onset": "Orphanet:216978", "HOP92": "EFO:0006440", "acute stress reaction": "EFO:0005223", "Escherichia coli Infections": "EFO:1001318", "Sinoatrial node dysfunction and deafness": "Orphanet:324321", "trans-zeatin": "CHEBI:16522", "Hyperammonemia due to N-acetylglutamate synthetase deficiency": "Orphanet:927", "observational design": "EFO:0000629", "pharyngoconjunctival fever": "EFO:0007434", "Neutral lipid storage disease": "Orphanet:165", "C2C12": "EFO:0001098", "Macaca radiata": "NCBITaxon:9548", "TT": "EFO:0002382", "KARPAS-620": "EFO:0006449", "pedicel": "PO:0009052", "Coralliform cataract": "Orphanet:98990", "Dickkopf-related protein 4 measurement": "EFO:0008110", "lung fibroblast derived cell line": "EFO:0005742", "echovirus infectious disease": "EFO:0007247", "HuNS1": "EFO:0002207", "PEO4": "EFO:0005448", "Central hypotonia {http": "HP:0011398", "Appendix Goblet Cell Carcinoid": "EFO:1000090", "stamen {http": "PO:0009029", "Finger syndactyly {http": "HP:0006101", "Currarino triad": "Orphanet:1552", "LCAT deficiency": "Orphanet:650", "forskolin": "CHEBI:42471", "Homozygous familial hypercholesterolemia": "Orphanet:391665", "Dentinogenesis imperfecta type 3": "Orphanet:166265", "paratyphoid fever": "EFO:0007420", "Myelitis": "EFO:1001472", "DG75": "EFO:0002160", "acesulfame {http": "CHEBI:83501", "skin conductance response amplitude": "EFO:0006868", "Malignant epithelial tumor of ovary": "Orphanet:398934", "torus lateralis": "UBERON:2000294", "Partial duplication of chromosome 11": "Orphanet:262653", "LHCN-M2": "EFO:0005714", "Pneumocystis infectious disease": "EFO:0007447", "BxPC-3": "EFO:0002709", "breast fibrosis": "EFO:1000145", "Prostate Small Cell Carcinoma": "EFO:1000499", "TCR Chain Paring": "EFO:0008966", "Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities": "Orphanet:77300", "Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation": "Orphanet:178396", "Spartina anglica": "NCBITaxon:49785", "Episodic ataxia type 4": "Orphanet:79136", "RNAlater specimen": "EFO:0005125", "Synechococcus phage S-PM2": "NCBITaxon:238854", "contactin-2 measurement": "EFO:0008100", "VCaP": "EFO:0007752", "Congenital patella dislocation": "Orphanet:295036", "assay by instrument": "EFO:0002773", "alcoholic cardiomyopathy": "EFO:1000801", "rhinosporidiosis": "EFO:0007471", "ML-DmD8": "EFO:0005832", "Mitochondrial disorder due to a defect in mitochondrial protein synthesis": "Orphanet:35696", "depressive episode measurement": "EFO:0007704", "Fuchs' endothelial dystrophy": "EFO:0003946", "CS57732": "EFO:0000078", "neutrophil-to-lymphocyte ratio": "EFO:0008447", "Retinal macular dystrophy type 2": "Orphanet:319640", "CD69-positive double-positive thymocyte": "CL:0002429", "HL-1 cell": "BTO:0003264", "3-hydroxyisobutyric aciduria": "Orphanet:939", "oral tuberculosis": "EFO:0007407", "Isolated anorectal malformation": "Orphanet:557", "GM12867": "EFO:0005340", "8988T": "EFO:0005713", "cleavage 2-cell": "EFO:0001285", "Fusarium globosum": "NCBITaxon:78864", "9-cis-retinoic acid": "CHEBI:50648", "ILSXISS51/TejJ": "EFO:0002987", "HSV1 seropositivity": "EFO:0007050", "Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15": "Orphanet:98754", "syphilitic aortitis": "EFO:1001206", "HCC1008": "EFO:0002057", "Charcot-Marie-Tooth disease type 4H": "Orphanet:99954", "GM12155": "EFO:0001140", "luteinizing hormone measurement": "EFO:0007002", "Obesity due to congenital leptin deficiency": "Orphanet:66628", "Kc167": "EFO:0005819", "somite 4": "UBERON:2000857", "Lotus filicaulis": "NCBITaxon:264956", "alternatively activated macrophage": "CL:0000890", "mediastinum": "UBERON:0003728", "Plasmodium knowlesi": "NCBITaxon:5850", "Rosa chinensis": "NCBITaxon:74649", "Dentin dysplasia type I": "Orphanet:99789", "skin conductance response frequency": "EFO:0006869", "Serratia Infections": "EFO:1001421", "response to clopidogrel": "GO:1903493", "Chronic diarrhea with hereditary sensory and autonomic neuropathy": "Orphanet:397606", "complex regional pain syndrome": "EFO:1001998", "serous cystadenofibroma": "EFO:0002510", "Symbrachydactyly of hands and feet": "Orphanet:1570", "cell outer membrane": "GO:0009279", "GM12144": "EFO:0001136", "Prochlorococcus marinus str. MIT 9312": "NCBITaxon:74546", "ventral midline glia": "FBbt:00001315", "Autosomal dominant Alport syndrome": "Orphanet:88918", "NCI-H920": "EFO:0006698", "Ectodermal dysplasia - blindness": "Orphanet:1806", "Senior-Boichis syndrome": "Orphanet:84081", "Saccharomyces boulardii": "NCBITaxon:252598", "Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome": "Orphanet:309854", "chemical entity": "CHEBI:24431", "GM12044": "EFO:0001133", "IgG memory B cell": "CL:0000979", "ventral sensory complex primordium": "FBbt:00005552", "progesterone measurement": "EFO:0007004", "Escherichia coli DH1": "NCBITaxon:536056", "HUES49": "EFO:0007084", "Dianzani autoimmune lymphoproliferative disease": "Orphanet:275523", "fluoride poisoning": "EFO:1001328", "response to ziprasidone": "GO:0097337", "floral organ meristem development stage {http": "PO:0007601", "thymocyte": "CL:0000893", "Familial thrombocytosis": "Orphanet:71493", "trans-4-hydroxy-D-proline {http": "CHEBI:27992", "Intellectual disability - hypoplastic corpus callosum - preauricular tag": "Orphanet:1495", "ILSXISS97/TejJ": "EFO:0003000", "Pigmentation disorder with eye involvement, excluding albinism": "Orphanet:98708", "X-linked hyper-IgM syndrome": "Orphanet:101088", "spermathecum": "UBERON:0000994", "endometrium adenocarcinoma": "EFO:0005232", "Glycogen storage disease due to acid maltase deficiency, juvenile onset": "Orphanet:308573", "nucleic acid library construction protocol": "EFO:0004184", "CS57691": "EFO:0000061", "heart rate variability measurement": "EFO:0008003", "Hermansky-Pudlak syndrome with pulmonary fibrosis": "Orphanet:231500", "Calypte anna": "NCBITaxon:9244", "Hs 839.T": "EFO:0006591", "IgG-positive double negative memory B cell": "CL:0002103", "Isolated focal cortical dysplasia type IIa": "Orphanet:269001", "Calver ecotype": "EFO:0005164", "Bifidobacterium bifidum": "NCBITaxon:1681", "X-linked recessive hereditary axonal motor and sensory neuropathy": "Orphanet:140462", "Femoral agenesis/hypoplasia, unilateral": "Orphanet:295065", "Genochondromatosis type 2": "Orphanet:93398", "peritoneal macrophage": "CL:0000581", "Respiratory Syncytial Virus Infection": "EFO:1001413", "AU565": "EFO:0001087", "GM17201 {http": "CLO:0013839", "Generalized congenital lipodystrophy with myopathy": "Orphanet:228429", "outbred": "EFO:0004430", "cyclooxygenase 2 inhibitor": "CHEBI:50629", "presumptive blood": "UBERON:0006596", "Orchesella cincta": "NCBITaxon:48709", "central corneal thickness": "EFO:0005213", "dysthymic disorder": "EFO:0008623", "pancolitis": "EFO:0005626", "SPRET/EiJ": "EFO:0007734", "Bordetella Infections": "EFO:1001275", "Anal Melanoma": "EFO:1000080", "Congenital high-molecular-weight kininogen deficiency": "Orphanet:483", "Feingold syndrome type 1": "Orphanet:391641", "Coffea": "NCBITaxon:13442", "Prochlorococcus marinus str. MIT 9313": "NCBITaxon:74547", "blood viscosity": "EFO:0004301", "larval day 21-29": "EFO:0001308", "G141": "EFO:0006404", "Rocio virus": "NCBITaxon:64315", "anti-CTCF": "EFO:0005034", "Ptosis": "Orphanet:98578", "ILSXISS60/TejJ": "EFO:0003020", "light quantity regimen": "EO:0007078", "GM15226 {http": "CLO:0027486", "subarachnoid hemorrhage": "EFO:0000713", "resting double-positive thymocyte": "CL:0002427", "Congenital patella dislocation, unilateral": "Orphanet:295234", "positive regulation of ovulation": "GO:0060279", "radius bone mineral density": "EFO:0007933", "endometrium": "UBERON:0001295", "Congenital elbow dislocation": "Orphanet:295032", "allergic bronchopulmonary aspergillosis": "EFO:0007140", "endothelin-converting enzyme 1 measurement": "EFO:0008121", "Oculocutaneous albinism": "Orphanet:55", "airway wall thickness measurement": "EFO:0006898", "Illumina HiSeq 4000": "EFO:0008563", "Staphylococcus aureus subsp. aureus NCTC 8325": "NCBITaxon:93061", "Paramyxoviridae infectious disease": "EFO:0007419", "phospholipid": "CHEBI:16247", "Hyper-IgE syndrome": "Orphanet:331223", "bacterial exanthem": "EFO:1000671", "tibia fracture": "EFO:0003944", "Autosomal recessive spastic paraplegia type 48": "Orphanet:306511", "Polydactyly of a biphalangeal thumb": "Orphanet:93339", "X-linked intellectual disability, Wittner type": "Orphanet:3064", "Trigonocephaly - short stature - developmental delay": "Orphanet:3369", "pharyngeal pouch 1": "UBERON:0007122", "Sex Hormone-Producing Adrenal Cortex Adenoma": "EFO:1000523", "collectin-11 measurement": "EFO:0008088", "Congenital myopathy with internal nuclei and atypical cores": "Orphanet:319160", "Hepatic steatosis": "HP:0001397", "hippocampal volume": "EFO:0005035", "docosatrienoate {http": "CHEBI:78895", "APC-related attenuated familial adenomatous polyposis": "Orphanet:247806", "Deafness-onychodystrophy syndrome": "Orphanet:3231", "Theiler stage 8": "EFO:0004400", "ND00051 {http": "CLO:0029732", "embryonic central brain": "FBbt:00005662", "membrane": "GO:0016020", "antidepressant-induced visual impairment": "EFO:0006323", "ILSXISS103/TejJ": "EFO:0003004", "Early-onset spastic ataxia-neuropathy syndrome": "Orphanet:313772", "Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome": "Orphanet:314575", "Syndromic lymphedema": "Orphanet:89832", "Intermediate nemaline myopathy": "Orphanet:171433", "doxycycline": "CHEBI:50845", "Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome": "EFO:0009031", "Hereditary folate malabsorption": "Orphanet:90045", "Dihydropteridine reductase deficiency": "Orphanet:226", "cis-ketoconazole": "CHEBI:47519", "Colobomatous and areolar dystrophy": "Orphanet:98665", "Kennedy disease": "Orphanet:481", "Microtia - eye coloboma - imperforation of the nasolacrimal duct": "Orphanet:139450", "nestin positive islet-derived progenitor cell": "EFO:0002540", "purine-containing compound biosynthetic process": "GO:0072522", "serum zinc measurement": "EFO:0005268", "Perry syndrome": "Orphanet:178509", "quinidine": "CHEBI:28593", "response to venlafaxine": "EFO:0006328", "6-phosphogluconate dehydrogenase deficiency": "Orphanet:99135", "Picea sitchensis": "NCBITaxon:3332", "fungal meningitis": "EFO:1000942", "root hair": "PO:0000256", "Non-syndromic intestinal malformation": "Orphanet:108967", "Ulbright-Hodes syndrome": "Orphanet:3404", "Methylcobalamin deficiency type cblG": "Orphanet:2170", "CD4-positive type I NK T cell secreting interleukin-4": "CL:0000927", "embryonic day 9": "EFO:0007644", "callous-unemotional behaviour": "EFO:0005322", "aorta smooth muscle": "EFO:0002775", "Polyglucosan body myopathy": "Orphanet:397937", "constrictive pericarditis": "EFO:1000878", "quinoline": "CHEBI:17362", "antiphospholipid antibody measurement": "EFO:0005200", "smoking behaviour measurement": "EFO:0005671", "RedBS-Seq": "EFO:0008886", "Pulmonary capillary hemangiomatosis": "Orphanet:199241", "Brachydactyly type E": "Orphanet:93387", "study type (plant)": "EO:0007231", "PELVIS syndrome": "Orphanet:83628", "Triticum aestivum": "NCBITaxon:4565", "Central Cord Syndrome": "EFO:1001772", "Caki1": "EFO:0002149", "balanitis": "EFO:1000833", "Kaunas ecotype": "EFO:0006977", "cot filtration": "EFO:0004455", "H7-hESC": "EFO:0005904", "leukemoid reaction": "EFO:1001014", "GM17186 {http": "CLO:0013784", "CD24-positive, CD8 single-positive thymocyte": "CL:0002434", "Proteus mirabilis HI4320": "NCBITaxon:529507", "CMA-03/06": "EFO:0006553", "hip geometry": "EFO:0004685", "Illumina Genome Analyzer IIx standard manufacturer's protocol": "EFO:0005084", "Isolated growth hormone deficiency type IA": "Orphanet:231662", "pollination": "GO:0009856", "Gastric Hamartomatous Polyp": "EFO:1000271", "Cochliobolus lunatus": "NCBITaxon:5503", "Benign Samaritan congenital myopathy": "Orphanet:324581", "Autosomal dominant spastic paraplegia type 29": "Orphanet:101009", "GM15385 {http": "CLO:0026789", "presumptive hypochord": "UBERON:0006599", "Nanophthalmia": "Orphanet:35612", "Autoimmune polyendocrinopathy type 1": "Orphanet:3453", "cortisol secretion measurement": "EFO:0004642", "Streptococcus sanguinis SK36": "NCBITaxon:388919", "pluripotent stem cell": "CL:0002248", "Acinetobacter baumannii": "NCBITaxon:470", "GM08931 {http": "CLO:0011234", "environmental samples": "NCBITaxon:33858", "polymyositis": "EFO:0003063", "Mustela putorius furo": "NCBITaxon:9669", "Carney-Stratakis syndrome": "Orphanet:97286", "KHOS240S": "EFO:0002219", "KARPAS 299": "EFO:0005390", "Endometrial Mucinous Adenocarcinoma": "EFO:1000236", "gp41 C34 peptide, HIV measurement": "EFO:0008140", "15q overgrowth syndrome": "Orphanet:314585", "Osteochondrodysplatic nanism - deafness - retinitis pigmentosa": "Orphanet:2653", "Distal trisomy 22q": "Orphanet:96109", "metastatic prostate cancer": "EFO:0000196", "Alopecia antibody deficiency": "Orphanet:1006", "Lymphoepithelioma-Like Lung Carcinoma": "EFO:1000340", "Glaucoma - sleep apnea": "Orphanet:2085", "stomach diverticulum": "EFO:1001850", "PDZ-Seq": "EFO:0008857", "autoantibody measurement": "EFO:0004866", "congenital heart malformation": "EFO:0005269", "Rectal duplication": "Orphanet:171220", "2-hydroxybutyrate {http": "CHEBI:64552", "data format specification": "IAO:0000098", "GM17193 {http": "CLO:0013795", "Osteogenesis imperfecta type 1": "Orphanet:216796", "chronic kidney disease": "EFO:0003884", "genistein": "CHEBI:28088", "Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes": "Orphanet:166475", "disease": "EFO:0000408", "central endosperm {http": "PO:0006220", "antibody secreting cell": "CL:0000946", "Qualitative or quantitative defects of FKRP": "Orphanet:207119", "deviation(from_normal)": "PATO:0000069", "vermiform appendix": "UBERON:0001154", "gamma-delta T cell": "CL:0000798", "post-exercise hypotension": "EFO:1001828", "Terminal osseous dysplasia - pigmentary defects": "Orphanet:88630", "Rhabditida infectious disease": "EFO:0007468", "BT483": "EFO:0001095", "Renpenning syndrome": "Orphanet:3242", "Alexa Fluor 555": "EFO:0004968", "pseudobulbar palsy": "EFO:1001131", "Tc17 cell": "CL:0002128", "PR segment": "EFO:0005095", "aerial part": "EFO:0001901", "CB1370": "EFO:0004079", "AB SOLiD 4 System": "EFO:0004438", "AG13145 {http": "CLO:0022107", "basophil adenoma": "EFO:1000834", "glaucoma": "EFO:0000516", "magnesium": "CHEBI:25107", "abnormality of the lymphatic system": "HP:0100763", "calcium": "CHEBI:22984", "N-methyl-6-pyridone-3-carboxamide {http": "CHEBI:27410", "Isolated congenitally uncorrected transposition of the great arteries": "Orphanet:216718", "oligoarticular juvenile idiopathic arthritis": "EFO:1002019", "Undifferentiated Pancreatic Carcinoma": "EFO:1000606", "STT3A-CDG": "Orphanet:370921", "Congenital deformities of fingers": "Orphanet:294947", "Retinitis punctata albescens": "Orphanet:52427", "triple-negative breast cancer": "EFO:0005537", "Human herpesvirus 5 strain Towne": "NCBITaxon:10363", "m6A-seq": "EFO:0008790", "SW1088": "EFO:0002358", "TNF-related apoptosis-inducing ligand measurement": "EFO:0008300", "regulatory T cell": "CL:0000815", "sleep": "GO:0030431", "Congenital hypogonadotropic hypogonadism": "Orphanet:174590", "COLO320DM": "EFO:0002136", "Pineal Parenchymal Tumor of Intermediate Differentiation": "EFO:1000474", "sleep time": "EFO:0005274", "Cervical Adenoid Cystic Carcinoma": "EFO:1000161", "appendage": "UBERON:0000026", "AG11726 {http": "CLO:0022371", "ELF-1": "EFO:0005901", "DR26": "EFO:0004081", "HBL100": "EFO:0001167", "CS57699": "EFO:0000063", "cyclophosphamide hydrate": "CHEBI:4026", "454 GS sequencer": "EFO:0004431", "Neuroectodermal melanolysosomal disease": "Orphanet:33445", "5-HIAA measurement": "EFO:0005132", "GM17220 {http": "CLO:0014375", "duodenum": "UBERON:0002114", "Leishmania donovani": "NCBITaxon:5661", "chronic myelogenous leukemia": "EFO:0000339", "Aristolochia fimbriata": "NCBITaxon:158543", "ZR7530": "EFO:0001263", "olfactory pit": "UBERON:0005870", "X-linked hypophosphatemia": "Orphanet:89936", "interaction with host": "GO:0051701", "Genetic non-syndromic renal or urinary tract malformation": "Orphanet:357506", "anti-Bcl11a": "EFO:0005027", "stationary phase culture": "BTO:0001899", "Autosomal dominant Charcot-Marie-Tooth disease type 2P": "Orphanet:300319", "L-proline betaine {http": "CHEBI:35280", "Patent ductus arteriosus - bicuspid aortic valve - hand anomalies": "Orphanet:228190", "dorsal prothoracic pharyngeal muscle": "EFO:0000423", "Mosaic trisomy 10": "Orphanet:96063", "sex hormone": "CHEBI:50112", "response to platelet aggregation inhibitor": "GO:0061478", "orbitofrontal cortex": "UBERON:0004167", "SCaBER": "EFO:0002325", "Korean": "EFO:0003165", "COLO 800": "EFO:0006378", "thromboblast": "CL:0000828", "sulindac": "CHEBI:9352", "Intellectual disability-brachydactyly-Pierre Robin syndrome": "Orphanet:364577", "posterior lateral line placode": "UBERON:2001156", "serum gamma-glutamyl transferase measurement": "EFO:0004532", "congenic strain": "EFO:0004003", "Crassostrea ariakensis": "NCBITaxon:94323", "femoral cancer": "EFO:0007270", "Phocomelia, Schinzel type": "Orphanet:2879", "Autosomal monosomy": "Orphanet:102020", "carmoxirole hydrochloride": "CHEBI:64199", "Spinocerebellar ataxia type 11": "Orphanet:98767", "6-deoxotyphasterol": "CHEBI:20717", "epibranchial placode": "UBERON:0003078", "tropical spastic paraparesis": "EFO:0007527", "vomeronasal organ": "UBERON:0002255", "corpus uteri": "UBERON:0009853", "angle unit": "UO:0000121", "Escherichia coli CFT073": "NCBITaxon:199310", "X chromosome number anomaly with male phenotype": "Orphanet:263720", "alopecia areata": "EFO:0004192", "microRNA profiling by high throughput sequencing": "EFO:0002896", "Autosomal recessive axonal Charcot-Marie-Tooth disease type 2": "Orphanet:91024", "Woolly hair nevus": "Orphanet:79414", "ML-DmBG3-c2": "EFO:0005823", "microspore": "CL:0000252", "bovine virus diarrhea-mucosal disease": "EFO:0007181", "Tuberculosis, Avian": "EFO:1001440", "Qualitative or quantitative defects of myotilin": "Orphanet:209224", "bone marrow cancer cell": "BTO:0000583", "Moniezia benedeni": "NCBITaxon:218196", "contracture": "EFO:0003899", "Latino": "EFO:0003166", "Adenomatosis, Pulmonary": "EFO:1001258", "KMS-27": "EFO:0006616", "ovarian dysfunction": "EFO:0009003", "Chem-Seq": "EFO:0008683", "human granulocytic anaplasmosis": "EFO:0000777", "CS57779": "EFO:0000116", "Congenital muscular dystrophy without intellectual disability": "Orphanet:370980", "Disorder of sialic acid metabolism": "Orphanet:309319", "OCI-LY3": "EFO:0006710", "muscular channelopathy": "EFO:1001899", "Phenylketonuria": "Orphanet:716", "Distal renal tubular acidosis": "Orphanet:18", "Hyperostosis corticalis generalisata": "Orphanet:3416", "Low birth weight - dwarfism - dysgammaglobulinemia": "Orphanet:2621", "Temtamy syndrome": "Orphanet:1777", "Spondyloepimetaphyseal dysplasia congenita, Strudwick type": "Orphanet:93346", "Maternally-inherited Leigh syndrome": "Orphanet:255210", "endometrial neoplasm": "EFO:0004230", "myeloid suppressor cell": "CL:0000889", "iDES": "EFO:0008776", "cell cycle phase": "EFO:0007064", "Contractures - ectodermal dysplasia - cleft lip/palate": "Orphanet:1484", "low affinity immunoglobulin gamma Fc region receptor III-B measurement": "EFO:0008212", "chemokine (C-X-C motif) ligand 1 measurement": "EFO:0008083", "oleoyl ethanolamide {http": "CHEBI:71466", "atrioventricular ring": "UBERON:2005073", "Bordetella sp.": "NCBITaxon:28081", "GM17823 {http": "CLO:0016515", "Bardet-Biedl syndrome 9": "EFO:0009027", "Goldmann-Favre syndrome": "Orphanet:53540", "vulva sarcoma": "EFO:0002920", "formal thought disorder": "EFO:0004805", "ChAP-seq": "EFO:0008680", "pericarditis": "EFO:0007427", "respiratory system disease": "EFO:0000684", "CS57596": "EFO:0000027", "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency": "Orphanet:319547", "GM17771 {http": "CLO:0016646", "response to anti-thyroid drug": "EFO:0007838", "Infantile Krabbe disease": "Orphanet:206436", "Agnathia - holoprosencephaly - situs inversus": "Orphanet:990", "cat-scratch disease": "EFO:0007195", "Cy5 dye": "CHEBI:37989", "Pancoast tumor": "EFO:1001080", "Hereditary cerebral cavernous malformation": "Orphanet:221061", "primary biliary cirrhosis": "EFO:1001486", "Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies": "Orphanet:254758", "Pachycladon cheesemanii": "NCBITaxon:106773", "Microcephaly-thin corpus callosum-intellectual disability syndrome": "Orphanet:397951", "emphysema": "EFO:0000464", "Alopecurus myosuroides": "NCBITaxon:81473", "tissue-resident macrophage": "CL:0000864", "ventral ectoderm anlage": "FBbt:00004204", "OCI-AML5": "EFO:0006707", "late promyelocyte": "CL:0002151", "Panc 08.13": "EFO:0006470", "X-linked centronuclear myopathy": "Orphanet:596", "Congenital disorder of glycosylation with developmental anomaly": "Orphanet:371235", "Gallbladder Squamous Cell Carcinoma": "EFO:1000267", "presumptive diencephalon": "UBERON:0006222", "eye allergy": "EFO:0005751", "hypocholesterolemia": "HP:0003146", "Immunodeficiency due to an early component of complement deficiency": "Orphanet:169147", "hair follicle dermal papilla cell": "CL:0000346", "erythrasma": "EFO:1000696", "uveoparotid fever": "EFO:1001232", "high content screen of cells in a gene deletion library": "EFO:0007552", "liver endoderm": "EFO:0002577", "Fibrolamellar Carcinoma": "EFO:1000256", "Partial trisomy/tetrasomy of chromosome 5": "Orphanet:262211", "pathological entity": "MPATH:0", "duodenogastric reflux": "EFO:1000909", "urate measurement": "EFO:0004531", "GM17132 {http": "CLO:0015081", "progesterone": "CHEBI:17026", "treatment refractory schizophrenia": "EFO:0004609", "Pachycladon enysii": "NCBITaxon:414717", "20q13.33 microdeletion syndrome": "Orphanet:261311", "KPL1": "EFO:0002221", "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly": "Orphanet:402364", "mammary gland": "UBERON:0001911", "advanced heart failure": "EFO:0003149", "Camponotus floridanus": "NCBITaxon:104421", "famotidine": "CHEBI:4975", "Heart-hand syndrome, Slovenian type": "Orphanet:168796", "Benign concentric annular macular dystrophy": "Orphanet:251287", "FRAXF syndrome": "Orphanet:100974", "entorhinal area": "UBERON:0002728", "Marcus-Gunn syndrome": "Orphanet:91412", "Sickle cell - hemoglobin D disease": "Orphanet:251370", "Peri-Implantitis": "EFO:1001390", "C-C motif chemokine 5 measurement": "EFO:0008053", "Combined oxidative phosphorylation defect type 15": "Orphanet:319524", "129P1/ReJ": "EFO:0001331", "organism status": "EFO:0007063", "Homocystinuria without methylmalonic aciduria": "Orphanet:622", "neural cell": "CL:0002319", "pemphigus herpetiformis": "EFO:0008606", "HUES48": "EFO:0007083", "methyl mercuric(II) chloride": "CHEBI:28216", "olfactory epithelium": "UBERON:0001997", "experimental process": "EFO:0002694", "valine {http": "CHEBI:27266", "HAP-1": "EFO:0007598", "inhibitor role": "CHEBI:35222", "Spondyloepimetaphyseal dysplasia, matrilin-3 type": "Orphanet:156728", "oral cavity cancer": "EFO:0005570", "clindamycin": "CHEBI:3745", "HC toxin": "CHEBI:48028", "methotrexate": "CHEBI:44185", "Severe dermatitis-multiple allergies-metabolic wasting syndrome": "Orphanet:369992", "human herpesvirus 8 infection": "EFO:0002612", "Benign Ovarian Mixed Epithelial Tumor": "EFO:1000114", "glutaric acid {http": "CHEBI:17859", "JM1": "EFO:0002212", "Neisseria cinerea": "NCBITaxon:483", "embryonic dorsal apodeme": "FBbt:00005745", "Pigmentation disorder with eye involvement": "Orphanet:98700", "Genetic eye tumor": "Orphanet:183619", "glioblastoma multiforme": "EFO:0000519", "Balkan nephropathy": "EFO:0007164", "PacBio Sequel System": "EFO:0008630", "BC-3": "EFO:0002046", "toxin": "CHEBI:27026", "Oculodentodigital dysplasia": "Orphanet:2710", "Panc 05.04": "EFO:0006469", "diabetic neuropathy": "EFO:1000783", "Interventricular septum aneurysm": "Orphanet:99092", "Distal trisomy 9q": "Orphanet:96101", "hypochord": "UBERON:0003058", "Lymphangiosarcoma": "EFO:1000339", "trypanosomiasis": "DOID:10113", "haemopoietic system cell line": "EFO:0002883", "T-B+ severe combined immunodeficiency": "Orphanet:317416", "Lethal faciocardiomelic dysplasia": "Orphanet:1972", "Glaucoma associated with neural crest cell migration anomaly": "Orphanet:98632", "factor XI measurement": "EFO:0004694", "Congenital vertical talus, bilateral": "Orphanet:295203", "Sjogren syndrome": "EFO:0000699", "neuroschistosomiasis": "EFO:0007394", "Rhodobacter sphaeroides": "NCBITaxon:1063", "Short tarsus - absence of lower eyelashes": "Orphanet:2832", "GM14532 {http": "CLO:0031606", "Disorder of magnesium transport": "Orphanet:309848", "2-hydroxyglutaric acid {http": "CHEBI:17084", "Dyschondrosteosis - nephritis": "Orphanet:1765", "esophageal adenocarcinoma": "EFO:0000478", "Rare genetic developmental defect during embryogenesis": "Orphanet:183530", "trans/cis-18": "EFO:0006825", "G28T": "EFO:0006407", "CS57813": "EFO:0000127", "CCL4 measurement": "EFO:0004751", "response to cisplatin": "GO:0072718", "non ionic surfactant role": "CHEBI:38828", "Salmonella enterica subsp. enterica serovar Typhimurium": "NCBITaxon:90371", "Actinobacillus infectious disease": "EFO:1000793", "Rare disorder with hypogonadotropic hypogonadism": "Orphanet:181387", "Intercalary limb defects": "Orphanet:294927", "vulvovaginitis": "EFO:1001240", "Polyneuropathy - hand defect": "Orphanet:2926", "platelet-derived growth factor receptor beta measurement": "EFO:0008265", "dorsal anterior lateral line ganglion": "UBERON:2001312", "Autosomal dominant diffuse mutilating palmoplantar keratoderma": "Orphanet:307773", "Odontotrichomelic syndrome": "Orphanet:2723", "angioid streaks": "EFO:1000805", "peptidyl-prolyl cis-trans isomerase E measurement": "EFO:0008257", "Methanobrevibacter smithii": "NCBITaxon:2173", "Microcytic anemia with liver iron overload": "Orphanet:83642", "Merkel cell skin cancer": "EFO:1001471", "Familial mesial temporal lobe epilepsy with febrile seizures": "Orphanet:165805", "N-acetyl-L-leucine {http": "CHEBI:17786", "detergent role": "CHEBI:27780", "NCI-H3255": "EFO:0003123", "MSTO-211H": "EFO:0002839", "Gleason score measurement": "EFO:0007000", "Gorlin-Chaudhry-Moss syndrome": "Orphanet:2095", "Caudal duplication": "Orphanet:1756", "Isolated craniosynostosis": "Orphanet:139390", "Familial hypocalciuric hypercalcemia": "Orphanet:405", "Hyperinsulinism-hyperammonemia syndrome": "Orphanet:35878", "gastrula shield": "EFO:0001297", "SB146": "EFO:0004067", "granulomatous dermatitis": "EFO:1000705", "amphiprotic solvent role": "CHEBI:4836", "Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures": "Orphanet:363454", "Disorder of manganese transport": "Orphanet:309851", "Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome": "Orphanet:307936", "MDST8": "EFO:0006644", "small vessel stroke": "EFO:1001504", "ureterocele": "EFO:1001227", "free cholesterol measurement": "EFO:0008591", "Acro-fronto-facio-nasal dysostosis": "Orphanet:1784", "G122": "EFO:0006400", "vegetative shoot apex {http": "PO:0025223", "health trait": "EFO:0007652", "GM14533 {http": "CLO:0031607", "Aneurysm, False": "EFO:1001265", "dermatosis papulosa nigra": "EFO:1000686", "Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation": "Orphanet:309515", "insulin receptor measurement": "EFO:0008160", "Anteverted nares {http": "HP:0000463", "epithelium of bronchiole": "UBERON:0002051", "membrane part": "GO:0044425", "Rare genetic movement disorder": "Orphanet:183521", "age-related nuclear cataract": "HP:0011142", "pemphigus foliaceus": "EFO:0008601", "X-linked endothelial corneal dystrophy": "Orphanet:293621", "anterior spinal artery syndrome": "EFO:1000810", "Vibrio harveyi ATCC BAA-1116": "NCBITaxon:338187", "dorsal trunk specific anlage": "FBbt:00017010", "Preaxial polydactyly - colobomata - intellectual disability": "Orphanet:2921", "5p13 microduplication syndrome": "Orphanet:329802", "Preaxial polydactyly of toes": "Orphanet:295006", "cytomegalovirus seropositivity": "EFO:0007037", "X-linked recessive optic atrophy": "Orphanet:98678", "Vitamin B12-unresponsive methylmalonic acidemia type mut-": "Orphanet:79312", "oligogalacturonide": "CHEBI:62533", "finishing sequencing assay": "EFO:0004161", "Alpha-N-acetylgalactosaminidase deficiency": "Orphanet:3137", "inflammatory macrophage": "CL:0000863", "labelling protocol": "EFO:0003808", "vessel": "UBERON:0000055", "Tenosynovial Giant Cell Tumor": "EFO:1000562", "CD8-alpha-alpha-positive, alpha-beta intraepithelial T cell": "CL:0000915", "benzo(a)pyrene diolepoxide 1": "CHEBI:30614", "9q31.1q31.3 microdeletion syndrome": "Orphanet:401923", "hypersensitivity reaction disease": "EFO:1002003", "HIV mother to child transmission": "EFO:0004595", "Subependymoma": "EFO:1000553", "Pancreatic Precancerous Condition": "EFO:1000443", "penis": "UBERON:0000989", "GM12864": "EFO:0005337", "Cyanidioschyzon merolae": "NCBITaxon:45157", "calcium intake measurement": "EFO:0006521", "CyT49": "EFO:0007073", "Disorder of phenylalanine metabolism": "Orphanet:284814", "extrahepatic cholestasis": "EFO:1000933", "GM17824 {http": "CLO:0016516", "HCC38": "EFO:0001180", "germinal center B cell": "CL:0000844", "testicular hydrocele": "EFO:1001859", "Brachytelephalangic chondrodysplasia punctata": "Orphanet:79345", "hydrostatic pressure": "EFO:0000534", "Trifolium repens": "NCBITaxon:3899", "disseminated intravascular coagulation": "HP:0005521", "Partial duplication of chromosome 10": "Orphanet:262648", "cotyledon emergence stage": "PO:0007049", "Synechococcus elongatus": "NCBITaxon:32046", "isoleucine {http": "CHEBI:24898", "Metabolic myopathy": "Orphanet:98486", "Haplochromis burtoni": "NCBITaxon:8153", "NET-Seq": "EFO:0008826", "glycerophosphoglycerol {http": "CHEBI:5457", "Total spina bifida cystica": "Orphanet:268748", "Campylobacter coli": "NCBITaxon:195", "embryonic stage 4": "EFO:0005863", "intracranial embolism": "EFO:1000991", "Theiler stage 28": "EFO:0002588", "Human respiratory syncytial virus A strain Long": "NCBITaxon:11260", "4-ethylphenyl sulfate {http": "CHEBI:82932", "Autosomal dominant Charcot-Marie-Tooth disease type 2I": "Orphanet:99942", "allantoin {http": "CHEBI:15676", "Chondrodysplasia punctata, Toriello type": "Orphanet:79347", "rosette {http": "PO:0025615", "bursa of Fabricius": "UBERON:0003903", "interleukin 5 receptor subunit alpha measurement": "EFO:0008186", "Null syndrome": "Orphanet:280234", "Lynch syndrome": "Orphanet:144", "streptozotocin": "CHEBI:9288", "tumour of cranial and spinal nerves": "EFO:0002431", "immunoprecipitate": "EFO:0000541", "Stargardt disease": "Orphanet:827", "angiographic measurement": "EFO:0006512", "calcium/calmodulin-dependent protein kinase type 1 measurement": "EFO:0008062", "Rare hereditary thrombophilia": "Orphanet:217454", "Disorder of the gamma-glutamyl cycle": "Orphanet:79196", "CD4-positive, alpha-beta thymocyte": "CL:0000810", "Pongo pygmaeus": "NCBITaxon:9600", "Vaginal Squamous Cell Carcinoma": "EFO:1000620", "cardiac ventricle": "UBERON:0002082", "oxaliplatin": "CHEBI:31941", "chondrosarcoma": "EFO:0000333", "ventral mesoderm": "UBERON:2000083", "celecoxib": "CHEBI:41423", "Mikati-Najjar-Sahli syndrome": "Orphanet:2558", "cutaneous Leishmaniasis": "EFO:0005046", "Cryptophthalmia": "Orphanet:98562", "H9": "EFO:0003045", "Rare cataract": "Orphanet:98640", "pipecolate {http": "CHEBI:36110", "sphingosine {http": "CHEBI:16393", "Laccaria bicolor": "NCBITaxon:29883", "steroid inherited metabolic disorder": "EFO:0005590", "RS 39604 hydrochloride": "CHEBI:64081", "Agammaglobulinemia": "Orphanet:183669", "cartilage disease": "EFO:0005802", "response to quetiapine": "GO:0097335", "substrate type": "EFO:0005522", "Drop-seq sequencing protocol": "EFO:0008444", "Riboflavin transporter deficiency": "Orphanet:97229", "Short stature due to primary acid-labile subunit deficiency": "Orphanet:140941", "Oncorhynchus nerka": "NCBITaxon:8023", "Autosomal dominant cerebellar ataxia type 4": "Orphanet:94149", "Norrie disease": "Orphanet:649", "injury": "EFO:0000546", "Henoch-Schoenlein purpura": "EFO:1000965", "Combined oxidative phosphorylation defect type 8": "Orphanet:319504", "embryonic stage 16": "EFO:0005876", "Short rib-polydactyly syndrome": "Orphanet:1505", "Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency": "Orphanet:319552", "V6.5": "EFO:0006308", "interleukin-1 beta (Homo sapiens)": "EFO:0003794", "skin epithelioid hemangioma": "EFO:1001424", "C-C motif chemokine 3-like 1 measurement": "EFO:0008052", "autism": "EFO:0003758", "Gonosome number anomaly": "Orphanet:98156", "CS57631": "EFO:0000047", "Enchytraeus albidus": "NCBITaxon:6390", "SNES": "EFO:0008938", "prostate adenocarcinoma": "EFO:0000673", "Pongo sp.": "NCBITaxon:9603", "Atypical autism": "Orphanet:199627", "desmoplastic small round cell tumor": "EFO:1000895", "functional brain measurement": "EFO:0007849", "C-C motif chemokine 21 measurement": "EFO:0008048", "scale": "UBERON:0002542", "Cranio-osteoarthropathy": "Orphanet:1525", "interleukin 1 receptor-like 1 measurement": "EFO:0008168", "Ileal Neuroendocrine Tumor G1": "EFO:1000300", "Hidradenocarcinoma": "EFO:1000295", "mortality": "EFO:0004352", "NCI-H1648": "EFO:0003119", "abdominal cavity": "UBERON:0003684", "Marmota monax": "NCBITaxon:9995", "Osteodysplasty, Melnick-Needles type": "Orphanet:2484", "Adrenomyodystrophy": "Orphanet:977", "Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome": "Orphanet:329332", "myoblast": "CL:0000056", "trichostrongyloidiasis": "EFO:0007522", "flying phobia": "EFO:1001889", "Litopenaeus vannamei": "NCBITaxon:6689", "Genetic digestive tract tumor": "Orphanet:271835", "Scapuloperoneal spinal muscular atrophy": "EFO:1001992", "simvastatin": "CHEBI:9150", "purine ribonucleoside metabolic process": "GO:0046128", "colonic cancer cell line": "BTO:0000797", "milligram per square meter": "EFO:0004373", "Familial clubfoot due to 5q31 microdeletion": "Orphanet:293144", "Estland ecotype": "EFO:0006968", "optic cup area measurement": "EFO:0006940", "ocular onchocerciasis": "EFO:0007398", "GM15215 {http": "CLO:0027492", "Sandhoff disease, juvenile form": "Orphanet:309162", "Fused mandibular incisors": "Orphanet:2287", "subclavian steal syndrome": "EFO:1001195", "GM12761": "EFO:0001152", "spinal cord compression": "EFO:1001845", "Partial duplication of chromosome 3": "Orphanet:262201", "UMC11": "EFO:0002386", "THP-1": "EFO:0001253", "membranous glomerulonephritis": "EFO:0004254", "tiller": "EFO:0006815", "Growth delay due to insulin-like growth factor I resistance": "Orphanet:73273", "eosinophil percentage of leukocytes": "EFO:0007991", "ES-E14TG2a": "EFO:0006275", "X-linked spinocerebellar ataxia type 3": "Orphanet:85297", "platelet storage pool deficiency": "EFO:1001112", "Bile Duct Adenoma": "EFO:1000123", "muscularis mucosa": "UBERON:0006676", "methadone dose measurement": "EFO:0007907", "clopidogrel metabolite measurement": "EFO:0007966", "KMS-11": "EFO:0005694", "CS57883": "EFO:0000156", "nocodazole": "CHEBI:34892", "OV7": "EFO:0006459", "flower nectary {http": "PO:0009056", "horizontal septum": "UBERON:0003901", "Zellweger-like syndrome without peroxisomal anomalies": "Orphanet:50812", "Fragile X syndrome": "Orphanet:908", "GM17792 {http": "CLO:0016672", "respiratory system neoplasm": "EFO:0003853", "adrenaline": "CHEBI:33568", "adult acute myeloid leukemia": "EFO:1001934", "Toxoplasma gondii": "NCBITaxon:5811", "Hereditary benign intraepithelial dyskeratosis": "Orphanet:352657", "roxindole": "CHEBI:48558", "Gardner syndrome": "Orphanet:79665", "etiolation": "EFO:0007589", "unspecified peripheral T-cell lymphoma": "EFO:0000211", "Helicobacter hepaticus": "NCBITaxon:32025", "15q11q13 microduplication syndrome": "Orphanet:238446", "Yersinia pseudotuberculosis infectious disease": "EFO:1001246", "Nodular neuronal heterotopia": "Orphanet:2149", "Microphthalmia, Lenz type": "Orphanet:568", "twin-to-twin transfusion syndrome": "EFO:1001221", "Canis lupus familiaris": "NCBITaxon:9615", "Diazoxide-resistant hyperinsulinism": "Orphanet:276585", "Emiliania huxleyi CCMP1516": "NCBITaxon:280463", "Keratolytic winter erythema": "Orphanet:50943", "Hereditary sensory and autonomic neuropathy type 2": "Orphanet:970", "nucleoside phosphate biosynthetic process": "GO:1901293", "ATC Classification System": "EFO:0005634", "Mitochondrial disease": "Orphanet:68380", "pulmonary coin lesion": "EFO:1001133", "STA-ET-1": "EFO:0002862", "Rhodopseudomonas palustris CGA009": "NCBITaxon:258594", "Cutaneous Undifferentiated Pleomorphic Sarcoma": "EFO:1000212", "Partial deletion of chromosome 2": "Orphanet:261771", "S-nitrosoglutathione": "CHEBI:50091", "Ramos-Arroyo syndrome": "Orphanet:1051", "vestibular neuronitis": "EFO:0007537", "Non-acquired premature ovarian failure": "Orphanet:95710", "Spondylometaphyseal dysplasia - cone-rod dystrophy": "Orphanet:85167", "polysome": "GO:0005844", "Autosomal dominant Charcot-Marie-Tooth disease type 2Q": "Orphanet:329258", "angiopoietin-2 receptor measurement": "EFO:0006902", "Tay-Sachs disease, B1 variant": "Orphanet:309239", "psychomotor performance": "EFO:0004362", "RD": "EFO:0002315", "fasting": "EFO:0002756", "insulin-sensitizing drug": "CHEBI:50864", "SM1": "EFO:0002706", "3q26 microduplication syndrome": "Orphanet:96095", "Distal 16p11.2 microdeletion syndrome": "Orphanet:261222", "Lagos bat virus": "NCBITaxon:38766", "Arabidopsis": "NCBITaxon:3701", "CS57714": "EFO:0000070", "Lactococcus lactis subsp. cremoris MG1363": "NCBITaxon:416870", "NCI-H1792": "EFO:0002266", "Benign childhood occipital epilepsy, Panayiotopoulos type": "Orphanet:98815", "Posterior cortical atrophy": "Orphanet:54247", "Fetal akinesia-cerebral and retinal hemorrhage syndrome": "Orphanet:363409", "smooth muscle cell": "CL:0000192", "plant treatment": "EO:0001001", "Mycobacterium leprae": "NCBITaxon:1769", "Infiltrating Bladder Lymphoepithelioma-Like Carcinoma": "EFO:1000302", "age at menarche": "EFO:0004703", "T+ B+ severe combined immunodeficiency": "Orphanet:397802", "hair colour measurement": "EFO:0007822", "lymphocytic colitis": "EFO:1001294", "Necrobiotic Xanthogranuloma": "EFO:1001376", "Lymphedema - cerebral arteriovenous anomaly": "Orphanet:86914", "Syndromic epicanthus": "Orphanet:98574", "RIL-seq": "EFO:0008895", "Plantar Fasciitis": "EFO:1001909", "Anauxetic dysplasia": "Orphanet:93347", "Autosomal dominant hereditary sensory and autonomic neuropathy": "Orphanet:140474", "Podospora anserina": "NCBITaxon:5145", "androstenedione measurement": "EFO:0007972", "EL": "EFO:0007749", "recombinant congenic strain": "EFO:0004007", "suppurative periapical periodontitis": "EFO:1001202", "Brachydactyly - arterial hypertension": "Orphanet:1276", "SNP array": "EFO:0002703", "Free sialic acid storage disease": "Orphanet:834", "O-propanoylcarnitine {http": "CHEBI:28867", "cognitive decline": "HP:0001268", "gait apraxia": "EFO:1000944", "Genetic pancreatic disease": "Orphanet:165661", "non-alcoholic fatty liver disease": "EFO:0003095", "kidney papillary necrosis": "EFO:1001004", "WIDR": "EFO:0002389", "Juvenile Paget disease": "Orphanet:2801", "raphe magnus": "EFO:0002518", "epidermolysis bullosa dystrophica": "EFO:1000692", "Bulbospinal muscular atrophy of adult": "Orphanet:206707", "4,5-dianilinophthalimide": "CHEBI:53110", "CLN2 disease": "Orphanet:228349", "Salivary Gland Acinic Cell Carcinoma": "EFO:1000513", "hystidil-tRNA synthetase autoantibody measurement": "EFO:0007703", "T4 tumor stage": "EFO:0004944", "female accessory gland": "FBbt:00004914", "proximal portion of right coronary artery": "FMA:3804", "electric current unit": "UO:0000004", "TIVA": "EFO:0008971", "Scheie syndrome": "Orphanet:93474", "Seckel syndrome": "Orphanet:808", "surfactant role": "CHEBI:35195", "Plexiform Ameloblastoma": "EFO:1000487", "Hall-Riggs syndrome": "Orphanet:2107", "SHEP": "EFO:0006294", "GM17795 {http": "CLO:0016682", "cerebral atherosclerosis": "EFO:1000860", "gibberellin A4": "CHEBI:32902", "colorectal health": "EFO:0008460", "Cree leukoencephalopathy": "Orphanet:99854", "athletic endurance measurement": "EFO:0007818", "Bell's palsy": "EFO:0007167", "sessile serrated polyp": "EFO:0008523", "Postsynaptic congenital myasthenic syndromes": "Orphanet:98913", "Lactobacillus farciminis": "NCBITaxon:1612", "N-desmethylclozapine": "CHEBI:64050", "cytomegalovirus infection": "EFO:0001062", "17p13.3 microduplication syndrome": "Orphanet:217385", "Xeroderma pigmentosum variant": "Orphanet:90342", "neocortex": "UBERON:0001950", "GM17165 {http": "CLO:0013993", "biopsy number": "EFO:0000287", "Oomycetes {http": "NCBITaxon:4762", "fear of medical pain measurement": "EFO:0008339", "Chondrocalcinosis {http": "HP:0000934", "Male infertility due to obstructive azoospermia of genetic origin": "Orphanet:399998", "Pancreatic Vipoma": "EFO:1000445", "late cleavage stage embryo Ce": "EFO:0005502", "Ws-1": "EFO:0005157", "Chrysolophus amherstiae": "NCBITaxon:9088", "blastula 1k-cell": "EFO:0001274", "Pubic Symphysis Diastasis": "EFO:1001833", "Eubacterium rectale": "NCBITaxon:39491", "Microcephaly - cleft palate": "Orphanet:2521", "Apodia, bilateral": "Orphanet:295107", "Rhodococcus aetherivorans": "NCBITaxon:191292", "Partial congenital cataract": "Orphanet:98992", "extra or missing processual parts": "PATO:0001564", "minute": "UO:0000031", "Alpha-crystallinopathy": "Orphanet:98910", "chemerin measurement": "EFO:0004573", "Hyperuricemia - anemia - renal failure": "Orphanet:217330", "Disorder of tyrosine metabolism": "Orphanet:284818", "bullous pemphigoid": "EFO:0007187", "Myotonia permanens": "Orphanet:99735", "immature Vgamma2-negative thymocyte": "CL:0002408", "distal": "EFO:0001655", "Cap myopathy": "Orphanet:171881", "Rare genetic male infertility": "Orphanet:399980", "selective IgA deficiency disease": "EFO:1001929", "Hereditary hyperferritinemia with congenital cataracts": "Orphanet:163", "elicited macrophage": "CL:0000861", "BICR 31": "EFO:0006542", "GM17184 {http": "CLO:0013752", "Autosomal recessive spastic paraplegia type 15": "Orphanet:100996", "ILSXISS98/TejJ": "EFO:0003001", "eosinophil": "CL:0000771", "caudate-putamen": "UBERON:0005383", "Osteopetrosis": "Orphanet:2781", "cystatin-F measurement": "EFO:0008104", "endodermal sinus tumor": "EFO:0007252", "Cylindrical spirals myopathy": "Orphanet:171886", "X-linked complicated spastic paraplegia type 1": "Orphanet:306617", "gamma-Glu-Val {http": "CHEBI:68848", "Hyper-IgM syndrome without susceptibility to opportunistic infections": "Orphanet:183666", "marijuana dependence": "EFO:0004218", "Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual disability": "Orphanet:2435", "tunicamycin": "CHEBI:29699", "N-(indol-3-ylacetyl)glutamine {http": "CHEBI:70811", "low tension glaucoma": "EFO:1001022", "gamma-Glu-Tyr {http": "CHEBI:82969", "CS57619": "EFO:0000036", "N-acetylphenylalanine {http": "CHEBI:21626", "HK104": "EFO:0004065", "vitreous hemorrhage": "EFO:0008626", "leukocyte immunoglobulin-like receptor subfamily B member 2 measurement": "EFO:0008209", "homosexuality": "EFO:0008485", "Autosomal recessive primary microcephaly": "Orphanet:2512", "Arthroderma obtusum": "NCBITaxon:119676", "Hereditary methemoglobinemia": "Orphanet:621", "postmenopausal": "EFO:0002721", "coleorhiza emergence stage": "PO:0025475", "cellular response to pH": "GO:0071467", "Neisseria": "NCBITaxon:482", "neovascular glaucoma": "EFO:1001060", "CS57704": "EFO:0000065", "inferior parietal lobule": "UBERON:0006088", "Familial parathyroid adenoma": "Orphanet:99877", "Zostera marina": "NCBITaxon:29655", "Synechococcus sp. WH 8102": "NCBITaxon:84588", "Cerebro-reno-digital syndrome": "Orphanet:1396", "cerebral peduncle": "UBERON:0002623", "Lethal chondrodysplasia, Moerman type": "Orphanet:1420", "bovine respiratory disease complex": "EFO:0007180", "Haim-Munk syndrome": "Orphanet:2342", "14q24.1q24.3 microdeletion syndrome": "Orphanet:401935", "Panc 02.03": "EFO:0006466", "phyllodes tumor": "EFO:0000653", "Esophageal duplication cyst": "Orphanet:100047", "C-C motif chemokine 7 measurement": "EFO:0008054", "Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria": "Orphanet:99646", "Coats plus syndrome": "Orphanet:313838", "pinguecula": "EFO:1001824", "Brooke-Spiegler syndrome": "Orphanet:79493", "TTC549": "EFO:0005700", "Mycobacterium bovis BCG": "NCBITaxon:33892", "Alpha-mannosidosis": "Orphanet:61", "antinematodal drug": "CHEBI:35444", "Hypoinsulinemic hypoglycemia and body hemihypertrophy": "Orphanet:293964", "high fat diet": "EFO:0002757", "central nervous system venous angioma": "EFO:1001774", "infect": "OBI:1110021", "Human herpesvirus 4": "NCBITaxon:10376", "cell death": "GO:0008219", "insomnia": "EFO:0004698", "Abnormality of facial skeleton": "HP:0011821", "Central diabetes insipidus": "HP:0000863", "Pai syndrome": "Orphanet:1993", "portal hypertension": "EFO:0000666", "imetit dihydrobromide": "CHEBI:64151", "Glycogen storage disease due to LAMP-2 deficiency": "Orphanet:34587", "intellectual developmental disorder with dysmorphic facies and ptosis": "EFO:0009070", "LAPC-9": "EFO:0005393", "retinal vasculitis": "EFO:1001156", "medial collateral ligament": "EFO:0001967", "Bernard-Soulier syndrome": "Orphanet:274", "uric acid": "CHEBI:27226", "tooth eruption": "GO:0044691", "Monosomy 22q13": "Orphanet:48652", "HUES8": "EFO:0007093", "HIV-associated neurocognitive disorder": "EFO:0007948", "(2Z,3Z)-bis\\\\\\{amino[(2-aminophenyl)sulfanyl]methylidene\\\\\\}butanedinitrile": "CHEBI:64208", "ephrin type-A receptor 1 measurement": "EFO:0008123", "growth abnormality": "HP:0001507", "Isochromosomy Yq": "Orphanet:98798", "lumpy skin disease": "EFO:0007349", "Dopamine beta-hydroxylase deficiency": "Orphanet:230", "Anophthalmia - microphthalmia": "Orphanet:98555", "enrichment protocol": "EFO:0009089", "OVMANA": "EFO:0006726", "Eisenia fetida": "NCBITaxon:6396", "Campylobacter jejuni subsp. jejuni 81-176": "NCBITaxon:354242", "Transient familial neonatal hyperbilirubinemia": "Orphanet:2312", "3-methyl-2-oxovalerate {http": "CHEBI:28654", "polybrominated diphenyl ether measurement": "EFO:0007962", "Hepatopulmonary Syndrome": "EFO:1001346", "Plasmopara viticola {http": "NCBITaxon:143451", "Colon Dysplasia": "EFO:1000183", "Ippy virus": "NCBITaxon:55096", "arsenic trichloride": "CHEBI:63952", "END-seq": "EFO:0008729", "bacterial disease": "EFO:0000771", "European bat lyssavirus 2": "NCBITaxon:57483", "PK-59": "EFO:0006736", "5-nonyloxytryptamine oxalate": "CHEBI:64147", "adductor mandibulae": "UBERON:0011683", "RNA-seq of coding RNA": "EFO:0003738", "seminiferous tubules": "EFO:0001404", "gestational age": "EFO:0005112", "Nilaparvata lugens {http": "EO:0007317", "Partial deletion of the short arm of chromosome 5": "Orphanet:261893", "Congenital erythropoietic porphyria": "Orphanet:79277", "Picea abies": "NCBITaxon:3329", "CS57758": "EFO:0000089", "X-linked intellectual disability - epilepsy - progressive joint contractures - dysmorphism": "Orphanet:85319", "Cafeteria roenbergensis": "NCBITaxon:33653", "Disease with diffuse palmoplantar keratoderma as a major feature": "Orphanet:307711", "non-alcoholic steatohepatitis": "EFO:1001249", "Generalized pseudohypoaldosteronism type 1": "Orphanet:171876", "respiratory paralysis": "EFO:1001840", "Maternal hyperphenylalaninemia": "Orphanet:2209", "Cheilitis": "HP:0100825", "Isolated punctate palmoplantar keratoderma": "Orphanet:2338", "Tracheal Adenoid Cystic Carcinoma": "EFO:1000598", "Frontal encephalocele": "Orphanet:1931", "block": "EFO:0005067", "SKMC": "EFO:0002801", "Neonatal Marfan syndrome": "Orphanet:284979", "Bifidobacterium animalis subsp. lactis": "NCBITaxon:302911", "Chondroid Hamartoma": "EFO:1000175", "GM15061 {http": "CLO:0030324", "response to fluoroquinolones": "EFO:0007920", "Illumina HiSeq X": "EFO:0008567", "ionic salt": "EFO:0004415", "fruit {http": "PO:0009001", "Endometrial Clear Cell Adenocarcinoma": "EFO:1000231", "Hypocalcemic vitamin D-dependent rickets": "Orphanet:289157", "assay by sequencer": "EFO:0003740", "Peroxisome biogenesis disorder-Zellweger syndrome spectrum": "Orphanet:79189", "cleavage 4-cell": "EFO:0001287", "CS57706": "EFO:0000067", "Ornithine transcarbamylase deficiency": "Orphanet:664", "particulate matter air pollution measurement": "EFO:0008255", "Arabidopsis arenosa": "NCBITaxon:38785", "appendicitis": "EFO:0007149", "Familial progressive hyper- and hypopigmentation": "Orphanet:280628", "N-acetyl-D-glucosamine kinase measurement": "EFO:0008239", "mercury dichloride": "CHEBI:31823", "lymphotactin measurement": "EFO:0008214", "Glycerol kinase deficiency, juvenile form": "Orphanet:284411", "Ocular Melanoma": "EFO:1000403", "Chondroid Chordoma": "EFO:1000174", "vulvitis": "EFO:1001239", "lateral line system": "UBERON:0002540", "vesiculobullous skin disease": "EFO:1000774", "HL-60": "EFO:0002793", "common lymphoid progenitor": "CL:0000051", "GM11829": "EFO:0001117", "conidium": "CL:0000599", "Filipino": "EFO:0003160", "GM19238": "EFO:0002788", "basophil mast progenitor cell": "CL:0002028", "planned process": "EFO:0004542", "hypopharyngeal sense organ primordium": "FBbt:00016001", "seedling development stage": "PO:0007131", "metoprolol": "CHEBI:6904", "GM14454 {http": "CLO:0031254", "HEL9217": "EFO:0002193", "Rare hereditary hemochromatosis": "Orphanet:220489", "Disorder of carbohydrate metabolism": "Orphanet:79161", "Distal monosomy 1q": "Orphanet:36367", "Lake Victoria marburgvirus - Angola2005": "NCBITaxon:378830", "damage intensity": "EFO:0000391", "Morgagni-Stewart-Morel syndrome": "Orphanet:77296", "panic disorder": "EFO:0004262", "AG13150 {http": "CLO:0022101", "Autosomal dominant spastic paraplegia type 41": "Orphanet:320355", "CB4853": "EFO:0004052", "MOLT-3": "EFO:0005265", "Camptodactyly - taurinuria": "Orphanet:1325", "Ring chromosome 6": "Orphanet:1448", "SKBR3": "EFO:0001236", "atopy": "EFO:0002686", "nucleobase-containing compound metabolic process": "GO:0006139", "Trisomy 20p": "Orphanet:261318", "arthritis": "EFO:0005856", "A/J": "EFO:0001327", "xylitol {http": "CHEBI:17151", "Isolated adermatoglyphia": "Orphanet:289465", "GM17187 {http": "CLO:0013775", "esophagus mucosa": "UBERON:0002469", "Miscanthus x giganteus": "NCBITaxon:183674", "Congenital reticular ichthyosiform erythroderma": "Orphanet:281190", "Lu135": "EFO:0002828", "aspartate(2-) {http": "CHEBI:29995", "elevated carbon dioxide treatment {http": "EO:0001056", "cystine {http": "CHEBI:17376", "CLN8 disease": "Orphanet:228354", "humerus fracture": "EFO:0003943", "Caroli Disease": "EFO:1001286", "GM10842 {http": "CLO:0023784", "Isolated growth hormone deficiency type II": "Orphanet:231679", "early cardiac repolarization measurement": "EFO:0004885", "Drosophila C virus infection": "EFO:0000779", "Gr\u00c3\u00a4sbeck-Imerslund disease": "Orphanet:35858", "Distal hereditary motor neuropathy type 5": "Orphanet:139536", "Infantile onset spinocerebellar ataxia": "Orphanet:1186", "Abnormality of the outer ear": "HP:0000356", "Streptomyces turgidiscabies": "NCBITaxon:85558", "vascular leaf primordium {http": "PO:0000017", "X-linked intellectual disability, Armfield type": "Orphanet:85276", "future spinal cord": "UBERON:0006241", "maleate (-1) {http": "CHEBI:37156", "Parietal foramina with cleidocranial dysplasia": "Orphanet:251290", "pistillate inflorescence {http": "PO:0025598", "kuru": "EFO:1001008", "assay by molecule": "EFO:0002772", "circulating endothelial cell": "CL:0002342", "cadmium dichloride hemipentahydrate": "CHEBI:63938", "high content screening stage": "EFO:0007555", "Mycoplasma genitalium": "NCBITaxon:2097", "bone density conservation agent": "CHEBI:50646", "blood serum": "BTO:0000133", "Congenital valvular dysplasia": "Orphanet:1864", "blood component": "EFO:0001941", "Congenital absence of upper arm and forearm with hand present, unilateral": "Orphanet:295085", "Ovarian Transitional Cell Carcinoma": "EFO:1000435", "Autosomal recessive spastic paraplegia type 72": "Orphanet:401849", "Populus balsamifera": "NCBITaxon:73824", "BCKN-1": "EFO:0002049", "plant cell": "PO:0009002", "Myelocystocele": "Orphanet:268813", "Ehlers-Danlos syndrome, musculocontractural type": "Orphanet:2953", "Disorder of fatty acid oxidation and ketone body metabolism": "Orphanet:79174", "ICAM-1 measurement": "EFO:0004520", "SW872": "EFO:0002373", "middle ear": "UBERON:0001756", "parathyroid disease": "EFO:0005754", "leiomyosarcoma": "EFO:0000564", "lip morphology measurement": "EFO:0007845", "Familial cystic renal disease": "Orphanet:93587", "GM17231 {http": "CLO:0014341", "Chilaiditi Syndrome": "EFO:1001776", "hilar cholangiocarcinoma": "EFO:1001959", "Mowat-Wilson syndrome due to monosomy 2q22": "Orphanet:261537", "hatching pec-fin": "EFO:0001299", "experimental arthritis": "EFO:1001787", "Congenital isolated hyperinsulinism": "Orphanet:657", "Non-syndromic esophageal malformation": "Orphanet:108959", "Mitochondrial neurogastrointestinal encephalomyopathy": "Orphanet:298", "serum ceruloplasmin measurement": "EFO:0005139", "tonsil": "UBERON:0002372", "occupation-related stress disorder": "EFO:0005250", "Young adult-onset Parkinsonism": "Orphanet:2828", "Craniosynostosis - fibular aplasia": "Orphanet:1533", "Zlotogora-Ogur syndrome": "Orphanet:3253", "diabetes mellitus biomarker": "EFO:0006842", "Carthamus tinctorius": "NCBITaxon:4222", "Orofaciodigital syndrome type 9": "Orphanet:141007", "RM 82": "EFO:0002853", "Total spina bifida aperta": "Orphanet:268377", "Astley-Kendall dysplasia": "Orphanet:85175", "5-azacytidine": "CHEBI:2038", "Caliciviridae infectious disease": "EFO:0007189", "Micrencephaly - corpus callosum agenesis - abnormal genitalia": "Orphanet:2508", "dRNA-Seq": "EFO:0008719", "10-undecenoate {http": "CHEBI:83041", "childhood trauma measurement": "EFO:0007979", "estrone measurement": "EFO:0007970", "Loeys-Dietz syndrome": "Orphanet:60030", "Hypotonia with lactic acidemia and hyperammonemia": "Orphanet:137908", "Pseudohypoaldosteronism type 2A": "Orphanet:88938", "Simul-seq": "EFO:0008924", "CaOv3": "EFO:0002148", "gastrula stage": "UBERON:0000109", "Hereditary pheochromocytoma-paraganglioma": "Orphanet:29072", "pyloric antrum": "UBERON:0001165", "alpha-1-antichymotrypsin measurement": "EFO:0008019", "translocation": "EFO:0004024", "Schimke immuno-osseous dysplasia": "Orphanet:1830", "Leukodystrophy": "Orphanet:68356", "cadmium": "CHEBI:22977", "metabolic disease": "EFO:0000589", "lateral": "EFO:0001657", "feeding difficulties {http": "HP:0011968", "Oral cleft": "HP:0000202", "Qualitative or quantitative defects of emerin": "Orphanet:209188", "Bacillus weihenstephanensis": "NCBITaxon:86662", "Primary CD59 deficiency": "Orphanet:169464", "Epiblepharon": "Orphanet:99169", "Pure or complex X-linked spastic paraplegia": "Orphanet:320350", "allergy": "EFO:0003785", "freemartinism": "EFO:1000939", "Shewanella oneidensis MR-1": "NCBITaxon:211586", "folliculitis": "EFO:1000702", "segmentation 20-25 somites": "EFO:0001320", "Keratosis pilaris atrophicans": "Orphanet:498", "leptomeningeal metastases": "EFO:1001012", "Cleft lip/palate - deafness - sacral lipoma": "Orphanet:2003", "ciliopathy": "EFO:0003900", "PL-21": "EFO:0006473", "Mokola virus": "NCBITaxon:12538", "Fowler syndrome": "Orphanet:221126", "Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation": "Orphanet:324525", "2-oxoglutarate(2-) {http": "CHEBI:16810", "IB3-1": "EFO:0001194", "Curly hair-acral keratoderma-caries syndrome": "Orphanet:307766", "Inherited acute myeloid leukemia": "Orphanet:319465", "Genetic urogenital tract malformation": "Orphanet:156622", "novobiocin": "CHEBI:28368", "Adactyly of hand": "Orphanet:294931", "abdominal aortic raised atherosclerotic lesion": "EFO:0005601", "ND00259 {http": "CLO:0026349", "repulsive guidance molecule A measurement": "EFO:0008273", "primary Actinomycetales infectious disease": "EFO:1001122", "blastula 30%-epiboly": "EFO:0001277", "alpha macroglobulin measurement": "EFO:0004815", "Rectal Hyperplastic Polyp": "EFO:1000502", "staminate inflorescence {http": "PO:0025601", "2-hydroxyglutaric aciduria": "Orphanet:19", "monoclonal gammopathy": "EFO:0000203", "Nance-Horan syndrome": "Orphanet:627", "primary Anaplasmataceae infectious disease": "EFO:1001123", "GM13977": "EFO:0005346", "Human echovirus 18": "NCBITaxon:47506", "micromole": "UO:0000039", "pineal body": "UBERON:0001905", "neuron": "CL:0000540", "Sino-auricular heart block": "Orphanet:1260", "Hemoglobin E disease": "Orphanet:2133", "Bartsocas-Papas syndrome": "Orphanet:1234", "Sea-blue histiocytosis": "Orphanet:158029", "Mucopolysaccharidosis type 6, slowly progressing": "Orphanet:276223", "Heterorhabditis bacteriophora": "NCBITaxon:37862", "Distal hereditary motor neuropathy, Jerash type": "Orphanet:139552", "heart valve prosthesis": "EFO:0003906", "Gaucher disease - ophthalmoplegia - cardiovascular calcification": "Orphanet:2072", "dihydrotestosterone measurement": "EFO:0004909", "Recurrent Neisseria infections due to factor D deficiency": "Orphanet:169467", "Branchio-skeleto-genital syndrome": "Orphanet:1299", "Congenital primary megaureter": "Orphanet:617", "ME-180": "EFO:0006646", "dysplasia of cervix": "EFO:1000910", "HCS library protocol": "EFO:0007571", "array platform variation design": "EFO:0001764", "Graves ophthalmopathy": "EFO:1001466", "Angelman syndrome": "Orphanet:72", "Triticum durum": "NCBITaxon:4567", "Lactobacillus fructivorans": "NCBITaxon:1614", "CD14-positive dermal dendritic cell": "CL:0002526", "radicle {http": "PO:0020031", "HCC827": "EFO:0003137", "Catel-Manzke syndrome": "Orphanet:1388", "Harlequin ichthyosis": "Orphanet:457", "Pancreatic insufficiency - anemia - hyperostosis": "Orphanet:199337", "KHM-1B": "EFO:0006609", "ENCODE": "EFO:0002910", "host cell nucleus": "GO:0042025", "pregnancy induced alloimmunization": "EFO:0008462", "microscopy assay": "EFO:0002909", "Methylation Spanning Linker Library (MSLL) processing": "EFO:0004175", "Neutropenia - monocytopenia - deafness": "Orphanet:2690", "Angelman syndrome due to paternal uniparental disomy of chromosome 15": "Orphanet:98795", "Fusarium oxysporum": "NCBITaxon:5507", "Coronary-Subclavian Steal Syndrome": "EFO:1001297", "Partial deletion of the short arm of chromosome 3": "Orphanet:261875", "intracellular region of host": "GO:0043656", "kininogen-1 measurement": "EFO:0008198", "CHL1": "EFO:0002132", "Rare genetic epilepsy": "Orphanet:183512", "ILSXISS110/TejJ": "EFO:0003006", "Orofaciodigital syndrome type 14": "Orphanet:369902", "pathogen": "EFO:0000643", "Primary short bowel syndrome": "Orphanet:365563", "Recessive mitochondrial ataxia syndrome": "Orphanet:94125", "Buchnera aphidicola": "NCBITaxon:9", "Citrobacter koseri": "NCBITaxon:545", "posterior lateral plate mesoderm": "UBERON:0009910", "Type 11 collagen-related bone disorder": "Orphanet:93422", "blood-injection-injury phobia": "EFO:1001878", "consomic strain": "EFO:0004004", "Rhizomelic dysplasia, Patterson-Lowry type": "Orphanet:2831", "body ganglion": "UBERON:0007134", "Hereditary thrombophilia due to congenital protein S deficiency": "Orphanet:743", "Microphthalmia with limb anomalies": "Orphanet:1106", "response to gefitinib": "EFO:0007867", "TAmC-Seq": "EFO:0008961", "cholinergic antagonist": "CHEBI:48873", "3134": "EFO:0007069", "Spastic paraplegia - epilepsy - intellectual disability": "Orphanet:2816", "epithelium of esophagus {http": "UBERON:0001976", "urticaria": "EFO:0005531", "Pseudomonas infection": "EFO:0001076", "Late-onset distal myopathy, Markesbery-Griggs type": "Orphanet:98912", "NCI-H1666": "EFO:0002262", "Congenital brain dysgenesis due to glutamine synthetase deficiency": "Orphanet:71278", "trachea": "UBERON:0003126", "L1 syndrome": "Orphanet:275543", "gram per meter squared": "EFO:0002898", "lumbar disc degeneration": "EFO:0004994", "caesium chloride": "CHEBI:63039", "MM1": "EFO:0001219", "steroid hormone": "CHEBI:26764", "Bm3-delta B cell": "CL:0000963", "Cold-induced sweating syndrome-hyperthermia spectrum": "Orphanet:401993", "Rubinstein-Taybi syndrome due to 16p13.3 microdeletion": "Orphanet:353281", "Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis": "Orphanet:1112", "Pyrus hybrid cultivar": "NCBITaxon:239770", "Marden-Walker syndrome": "Orphanet:2461", "ES-CJ7": "EFO:0005916", "7q31 microdeletion syndrome": "Orphanet:251061", "Non-Seminomatous Lesion": "EFO:1000401", "Congenital absence/hypoplasia of fingers excluding thumb, unilateral": "Orphanet:973", "LCLC-103H": "EFO:0006634", "fibroblast of dermis": "CL:0002551", "Rare genetic myoclonus": "Orphanet:307064", "adult acute monocytic leukemia": "EFO:1001933", "Tetrasomy X": "Orphanet:9", "A1C measurement": "EFO:0004541", "Juvenile neuronal ceroid lipofuscinosis": "Orphanet:79264", "Genetic lipodystrophy": "Orphanet:98305", "Agenesis of the corpus callosum - intellectual disability - coloboma - micrognathia": "Orphanet:52055", "prolactin measurement": "EFO:0007003", "mouth neoplasm": "EFO:0003868", "suprachiasmatic nucleus": "UBERON:0002034", "Arabidopsis arenosa x Arabidopsis thaliana": "NCBITaxon:378006", "flavone": "CHEBI:42491", "Agrobacterium": "NCBITaxon:357", "Alkaptonuria": "Orphanet:56", "CS57769": "EFO:0000090", "reproductive system disease": "EFO:0000512", "IMR-90": "EFO:0001196", "Pituicytoma": "EFO:1000477", "Iridocorneal endothelial syndrome": "Orphanet:64734", "primitive olfactory epithelium": "UBERON:2001431", "scATAC-seq (Microfluidics)": "EFO:0008904", "dexibuprofen": "CHEBI:43415", "paraffin specimen": "OBI:0000950", "EcR-RKO/KLF4": "EFO:0002052", "tibial artery": "UBERON:0007610", "femoral neuropathy": "EFO:1000936", "Distal arthrogryposis": "Orphanet:97120", "Familial isolated congenital asplenia": "Orphanet:101351", "response to stavudine": "EFO:0006998", "Dysmorphism - conductive hearing loss - heart defect": "Orphanet:289553", "Schinzel-Giedion syndrome": "Orphanet:798", "behavior or behavioral disorder measurement": "EFO:0004782", "Trisomy X": "Orphanet:3375", "Episodic ataxia with slurred speech": "Orphanet:401953", "band form basophil": "CL:0000770", "Baller-Gerold syndrome": "Orphanet:1225", "Cryptococcus neoformans var. grubii H99": "NCBITaxon:235443", "glyphosate": "CHEBI:27744", "Semantic dementia": "Orphanet:100069", "facial depth measurement": "EFO:0007857", "Escherichia coli K-12": "NCBITaxon:83333", "genomic DNA": "EFO:0008479", "Recessive dystrophic epidermolysis bullosa inversa": "Orphanet:79409", "Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature": "Orphanet:269573", "Xanthomonas oryzae pv. oryzicola BLS256": "NCBITaxon:383407", "rhizome": "PO:0004542", "apolipoprotein A 1 measurement": "EFO:0004614", "West Nile encephalitis": "EFO:0007545", "G44": "EFO:0006408", "urinary bladder": "UBERON:0001255", "endomembrane system": "GO:0012505", "Childhood disintegrative disorder": "Orphanet:168782", "phytosterol": "CHEBI:28824", "tick paralysis": "EFO:0007509", "asymmetrical dimethylarginine measurement": "EFO:0006522", "chiro-inositol {http": "CHEBI:23098", "Glycogen storage disease due to phosphoglycerate mutase deficiency": "Orphanet:97234", "Leishmania major": "NCBITaxon:5664", "lymphoma": "EFO:0000574", "brain glioblastoma": "EFO:0006545", "granulosa cell tumor": "EFO:1000032", "mature CD14-positive dermal dendritic cell": "CL:0002528", "serum VEGFR2 concentration measurement": "EFO:0006795", "Oromandibular-limb hypogenesis syndrome": "Orphanet:2749", "1-4-dioxane": "CHEBI:47032", "Autosomal dominant Kenny-Caffey syndrome": "Orphanet:93325", "Lactobacillus sanfranciscensis": "NCBITaxon:1625", "Lophura nycthemera": "NCBITaxon:9046", "abnormal paneth cell measurement": "EFO:0007963", "somatostatinoma": "EFO:1001187", "monoclonal B-cell lymphocytosis": "EFO:0006889", "X-linked intellectual disability - dysmorphism - cerebral atrophy": "Orphanet:2958", "mesocotyl": "PO:0020037", "gas trapping measurement": "EFO:0007628", "Navajo neurohepatopathy": "Orphanet:255229", "Liver Cavernous Hemangioma": "EFO:1000322", "Orofaciodigital syndrome type 4": "Orphanet:2753", "invertebrate ganglion": "EFO:0000890", "ethionamide": "CHEBI:4885", "indole-3-acetate {http": "CHEBI:30854", "breast adenosis": "EFO:0006891", "Partial androgen insensitivity syndrome": "Orphanet:90797", "Blepharonasofacial malformation syndrome": "Orphanet:1252", "reticulocyte": "CL:0000558", "vagina": "UBERON:0000996", "Syndrome with brachydactyly": "Orphanet:69028", "Intellectual disability - polydactyly - uncombable hair": "Orphanet:3082", "griseofulvin": "CHEBI:27779", "Theiler stage 3": "EFO:0004395", "Cardiac anomalies - heterotaxy": "Orphanet:137628", "interferon alpha 2a": "EFO:0003022", "MPI-CDG": "Orphanet:79319", "3,3',4,4'-tetrachlorobiphenyl": "CHEBI:1367", "Drosophila simulans NC48": "EFO:0004031", "Intermediate DEND syndrome": "Orphanet:99989", "Mild hemophilia A": "Orphanet:169808", "diabetic cardiomyopathy": "EFO:1001458", "Pseudoachondroplasia": "Orphanet:750", "growth hormone measurement": "EFO:0008438", "NCI-N87": "EFO:0002841", "KOPT-K1": "EFO:0006283", "citrate(3-) {http": "CHEBI:16947", "Dense granule disease": "Orphanet:98456", "plastid part": "GO:0044435", "NCI-H2405": "EFO:0002288", "Urachal cyst": "Orphanet:488", "household air pollution measurement": "EFO:0006924", "hepatocyte growth factor receptor measurement": "EFO:0008153", "megakaryocyte progenitor cell": "CL:0000553", "small intestinal adenocarcinoma": "EFO:1000532", "GM17200 {http": "CLO:0013840", "X-linked intellectual disability - plagiocephaly": "Orphanet:2898", "Leukocyte adhesion deficiency type II": "Orphanet:99843", "ADAMTS13 activity measurement": "EFO:0006955", "Masticophis": "NCBITaxon:94898", "Goldberg-Shprintzen megacolon syndrome": "Orphanet:66629", "Apis florea": "NCBITaxon:7463", "childhood T acute lymphoblastic leukemia": "EFO:1001947", "Ectodermal malformation syndrome associated with ocular features": "Orphanet:98709", "Stiff-Person syndrome": "EFO:0007498", "3-[4-(3-chlorophenyl)piperazin-1-yl]-1,1-diphenylpropan-2-ol hydrochloride": "CHEBI:64057", "Jervell and Lange-Nielsen syndrome": "Orphanet:90647", "Dermatoosteolysis, Kirghizian type": "Orphanet:1657", "alcoholic psychosis": "EFO:1001260", "ammonium phosphate": "CHEBI:62982", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation": "Orphanet:397735", "Malignant Ovarian Mixed Epithelial Tumor": "EFO:1000358", "benign neoplasm": "EFO:0002422", "GM17143 {http": "CLO:0013937", "4-hydroxyphenyl retinamide": "CHEBI:42588", "mobile element identification design": "EFO:0005693", "8p23.1 microduplication syndrome": "Orphanet:251076", "Cerebellar ataxia with peripheral neuropathy": "Orphanet:207028", "adult endothelial progenitor cell": "CL:0002619", "sea-blue histiocyte syndrome": "EFO:1001170", "nilotinib": "CHEBI:52172", "embryo root {http": "PO:0000045", "prostate gland cancer cell": "BTO:0001130", "NW1229": "EFO:0005488", "Severe congenital neutropenia": "Orphanet:42738", "CD115-positive monocyte OR common dendritic progenitor": "CL:0001019", "Headache": "HP:0002315", "dual specificity mitogen-activated protein kinase kinase 4 measurement": "EFO:0008113", "Ostreococcus tauri": "NCBITaxon:70448", "herpes virus seropositivity": "EFO:0007036", "GM17236 {http": "CLO:0014336", "Radio-renal syndrome": "Orphanet:3015", "Renal glucosuria": "Orphanet:69076", "PE RAD-Seq": "EFO:0008858", "substantia nigra": "UBERON:0002038", "Hyperimmunoglobulinemia D with periodic fever": "Orphanet:343", "Acrofacial dysostosis, Weyers type": "Orphanet:952", "segmentation 10-13 somites": "EFO:0001318", "Congenital cornea plana": "Orphanet:53691", "Iranian": "EFO:0003162", "CCD-16Lu": "EFO:0005362", "Autosomal dominant cerebellar ataxia type 3": "Orphanet:94148", "Frontotemporal neurodegeneration with movement disorder": "Orphanet:306708", "7-chlorokynurenic acid": "CHEBI:63965", "macrophage activation syndrome": "EFO:1001806", "Mycobacterium tuberculosis H37Rv": "NCBITaxon:83332", "3q13 microdeletion syndrome": "Orphanet:1621", "Picea glauca": "NCBITaxon:3330", "gamma-tocopherol measurement": "EFO:0007899", "N-nitrosodiethylamine": "CHEBI:34873", "primitive erythroid progenitor": "CL:0002361", "common cold": "EFO:0007214", "Human adenovirus 41": "NCBITaxon:10524", "odontogenesis": "GO:0042476", "Undifferentiated Pancreatic Carcinoma with Osteoclast-Like Giant Cells": "EFO:1000607", "Microcephalic primordial dwarfism, Toriello type": "Orphanet:2643", "Short fifth metacarpals - insulin resistance": "Orphanet:66518", "fructose-bisphosphate aldolase measurement": "EFO:0004809", "Enterococcus faecalis infection": "EFO:0000780", "Complex Endometrial Hyperplasia": "EFO:1000202", "thyroid peroxidase antibody measurement": "EFO:0005666", "Phaeodactylum tricornutum": "NCBITaxon:2850", "echinococcosis": "EFO:0007245", "cadmium sulfate": "CHEBI:50292", "dendritic cell": "CL:0000451", "pristane": "CHEBI:53181", "GM17185 {http": "CLO:0013781", "joint disease": "EFO:1000999", "Smith-Lemli-Opitz syndrome": "Orphanet:818", "mitochondrial NADH": "CHEBI:38498", "renal elimination rate measurement": "EFO:0007649", "time series design": "EFO:0001779", "RIP-Chip by array": "EFO:0005517", "Pitt-Hopkins syndrome": "Orphanet:2896", "p-tau measurement": "EFO:0004763", "killer cell immunoglobulin-like receptor 2DL4 measurement": "EFO:0008197", "Multiple sclerosis - ichthyosis - factor VIII deficiency": "Orphanet:3151", "Expressive language delay {http": "HP:0002474", "Lactobacillus johnsonii": "NCBITaxon:33959", "Genetic congenital limb malformation": "Orphanet:183536", "SW1116": "EFO:0002359", "Swiss5": "EFO:0006301", "serum amyloid A-1 protein measurement": "EFO:0008282", "Osteopathia striata - pigmentary dermopathy - white forelock": "Orphanet:2779", "phytogenic insecticide": "CHEBI:22917", "Genetic renal or urinary tract malformation": "Orphanet:183539", "Sandhoff disease": "Orphanet:796", "descending thoracic aorta": "UBERON:0002345", "DNA array": "EFO:0002701", "SW1417": "EFO:0002361", "Other metabolic disease": "Orphanet:91088", "viral cardiomyopathy": "EFO:0002629", "dissection": "EFO:0003856", "qualitative": "PATO:0000068", "LP.04 four leaves visible stage": "PO:0007115", "placental hematopoietic stem cell": "CL:0002359", "Pseudo-von Willebrand disease": "Orphanet:52530", "Brown-Pearce carcinoma": "EFO:1001278", "blood molybdenum measurement": "EFO:0007582", "cadmium poisoning": "EFO:1001768", "ear protrusion": "EFO:0007665", "G59": "EFO:0006409", "CNS demyelinating autoimmune disease": "EFO:1000870", "46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency": "Orphanet:753", "Dyskeratosis congenita": "Orphanet:1775", "Fleck corneal dystrophy": "Orphanet:98970", "X-linked hypohidrotic ectodermal dysplasia": "Orphanet:181", "Monosomy 9p": "Orphanet:261112", "GM17770 {http": "CLO:0016647", "Genetic sebaceous gland anomaly": "Orphanet:183460", "placental insufficiency": "EFO:0007443", "HCC1143": "EFO:0001169", "Simple Endometrial Hyperplasia with Atypia": "EFO:1000526", "head visceral muscle primordium": "FBbt:00007049", "Autosomal recessive spastic paraplegia type 25": "Orphanet:101005", "diethylhexyl phthalate": "CHEBI:17747", "Hemoglobin H disease": "Orphanet:93616", "20q11.2 microduplication syndrome": "Orphanet:363659", "Rare genetic bone development disorder": "Orphanet:404584", "joint component": "EFO:0001958", "ureter urothelial carcinoma": "EFO:1001973", "MODY": "Orphanet:552", "adenoma {http": "EFO:0000232", "gamma wave measurement": "EFO:0008388", "Cucumis melo subsp. melo": "NCBITaxon:412675", "epithelial cell of large intestine": "CL:0002253", "Inherited non-syndromic ichthyosis": "Orphanet:281082", "body odor measurement": "EFO:0008386", "infant body height": "EFO:0006785", "Mobala virus": "NCBITaxon:55097", "Tobacco rattle virus": "NCBITaxon:12295", "Juvenile Polyp": "EFO:1000310", "Symphalangism with multiple anomalies of hands and feet": "Orphanet:3246", "MASA syndrome": "Orphanet:2466", "Congenital amegakaryocytic thrombocytopenia": "Orphanet:3319", "Pityriasis rubra pilaris": "Orphanet:2897", "allergen exposure measurement": "EFO:0007944", "Rolandic epilepsy - speech dyspraxia": "Orphanet:163721", "Listeria monocytogenes FSL J1-208": "NCBITaxon:393119", "embryonic day 15.5": "EFO:0002566", "tiling path by array": "EFO:0001031", "Hearing Loss, Noise-Induced": "EFO:1001338", "ILSXISS13/TejJ": "EFO:0002974", "Salmonella enterica subsp. enterica serovar Dublin": "NCBITaxon:98360", "Helicobacter pylori": "NCBITaxon:210", "Autosomal dominant palmoplantar keratoderma and congenital alopecia": "Orphanet:1010", "warm/hot temperature regimen {http": "EO:0007173", "Met5A": "EFO:0001218", "Autosomal dominant hypohidrotic ectodermal dysplasia": "Orphanet:1810", "Cataract-glaucoma": "Orphanet:162", "Enchondromatosis": "Orphanet:296", "SNU-216": "EFO:0006754", "interleukin 12 receptor subunit beta-1 measurement": "EFO:0008170", "CME-L1": "EFO:0005650", "menstrual cycle measurement": "EFO:0007786", "SKGT4": "EFO:0001237", "GM17226 {http": "CLO:0014356", "Multicystic dysplastic kidney": "Orphanet:1851", "(S)-azetidine-2-carboxylic acid": "CHEBI:6198", "Sebocystomatosis": "Orphanet:841", "protein assay": "EFO:0001458", "empty sella syndrome": "EFO:1000914", "Bethlem myopathy": "Orphanet:610", "intermediate coronary syndrome": "EFO:1000985", "Blepharophimosis - epicanthus inversus - ptosis due to a point mutation": "Orphanet:261572", "IGF-1 measurement": "EFO:0004627", "aluminium": "CHEBI:28984", "Familial infantile bilateral striatal necrosis": "Orphanet:225154", "Familial primary hypomagnesemia": "Orphanet:34526", "instrument part": "EFO:0005060", "GM17846 {http": "CLO:0016456", "Coffea arabica": "NCBITaxon:13443", "P-Selectin measurement": "EFO:0008254", "nucleate erythrocyte": "CL:0000562", "Pancreatic triacylglycerol lipase deficiency": "Orphanet:309031", "tabes dorsalis": "EFO:0007505", "YFP protein fusion library": "EFO:0007567", "Keratoconus": "Orphanet:156071", "Clostridium kluyveri": "NCBITaxon:1534", "Papillary Transitional Cell Carcinoma": "EFO:1000450", "Hypoketotic hypoglycemia": "HP:0001985", "46,XY gonadal dysgenesis - motor and sensory neuropathy": "Orphanet:168563", "atypical ductal hyperplasia": "EFO:0008491", "renal osteodystrophy": "EFO:1001152", "angiotensin II": "CHEBI:48432", "size fractionation": "EFO:0004183", "congenital toxoplasmosis": "EFO:0007220", "SK23": "EFO:0006490", "myo-inositol {http": "CHEBI:17268", "DNA-seq": "EFO:0002693", "Borderline Exocrine Pancreatic Neoplasm": "EFO:1000133", "diaphragm": "UBERON:0001103", "Geleophysic dysplasia": "Orphanet:2623", "nosophobia": "EFO:1001903", "Canton S": "EFO:0001325", "CS57771": "EFO:0000112", "Cystic Nephroma": "EFO:1000213", "Primary dystonia, DYT17 type": "Orphanet:370103", "hypopharynx anlage in statu nascendi": "FBbt:00016000", "nevus": "EFO:0000625", "Lelis syndrome": "Orphanet:140936", "4-guanidinobutanoate {http": "CHEBI:86392", "phenol": "CHEBI:15882", "Osteopathia striata - cranial sclerosis": "Orphanet:2780", "SKOV3": "EFO:0002340", "adult acute megakaryoblastic leukemia": "EFO:1001932", "deletion": "EFO:0004014", "louping ill": "EFO:0007348", "Camptobrachydactyly": "Orphanet:1319", "Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency": "Orphanet:319595", "Congenital prekallikrein deficiency": "Orphanet:749", "Ocular motor apraxia, Cogan type": "Orphanet:1125", "laryngeal neoplasm": "EFO:0003817", "Distal trisomy 6q": "Orphanet:96098", "interleukin 16 measurement": "EFO:0008173", "Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency": "Orphanet:308410", "sphingosine 1-phosphate": "CHEBI:37550", "DR20": "EFO:0004080", "Syndromic ankyloblepharon": "Orphanet:98565", "GM13883 {http": "CLO:0033199", "Enterococcus faecalis OG1RF": "NCBITaxon:474186", "SK-MEL-24": "EFO:0006487", "spinal stenosis": "EFO:0007490", "Pelizaeus-Merzbacher disease, connatal form": "Orphanet:280210", "Alpha-thalassemia - intellectual disability syndrome linked to chromosome 16": "Orphanet:98791", "testosterone measurement": "EFO:0004908", "electrical current": "EFO:0000388", "maximal oxygen uptake measurement": "EFO:0004887", "cognitive disorder": "EFO:1001457", "Crigler-Najjar syndrome type 1": "Orphanet:79234", "fenpropimorph": "CHEBI:50148", "Familial angiolipomatosis": "Orphanet:199279", "Distal 7q11.23 microdeletion syndrome": "Orphanet:254351", "Retinitis pigmentosa": "Orphanet:791", "whooping cough": "EFO:0000650", "biotin metabolic process": "GO:0006768", "Phalangeal microgeodic syndrome": "Orphanet:352636", "Ly49H-negative natural killer cell": "CL:0002448", "ivermectin": "CHEBI:6078", "Mycoplasmatales Infections": "EFO:1001374", "CCD-33Lu": "EFO:0005366", "Testicular Leydig Cell Tumor": "EFO:1000569", "signal transduction": "GO:0007165", "balantidiasis": "EFO:0007163", "SE.02 two nodes or internodes visible stage {http": "PO:0007117", "testicular neoplasm": "EFO:0004281", "SUIT-2": "EFO:0006495", "mature CD16-positive myeloid dendritic cell": "CL:0002534", "Partial monosomy of the long arm of chromosome 9": "Orphanet:262074", "Ascaridida infectious disease": "EFO:0007156", "Char syndrome": "Orphanet:46627", "Familial glucocorticoid deficiency": "Orphanet:361", "Diazoxide-resistant diffuse hyperinsulinism": "Orphanet:165988", "ammonium": "CHEBI:28938", "Medium chain acyl-CoA dehydrogenase deficiency": "Orphanet:42", "Pancreatoblastoma": "EFO:1000446", "nafadotride": "CHEBI:64191", "CATCH-IT": "EFO:0008677", "tuberculous empyema": "EFO:0007528", "diet measurement": "EFO:0008111", "Crocosphaera watsonii WH 8501": "NCBITaxon:165597", "LP/J": "EFO:0007733", "Disorder of proline metabolism": "Orphanet:289866", "instrument": "EFO:0000548", "Autosomal recessive hypohidrotic ectodermal dysplasia": "Orphanet:248", "D-mannitol": "CHEBI:16899", "Roifman syndrome": "Orphanet:353298", "campesterol {http": "CHEBI:28623", "Illumina HiSeq 2000 standard manufacturer's protocol": "EFO:0005086", "Genetic malformation syndrome with odontal and/or periodontal component": "Orphanet:183580", "Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome": "Orphanet:391408", "L4 larva": "EFO:0005509", "Autosomal recessive cutis laxa type 2B": "Orphanet:357064", "Tel Hashomer camptodactyly syndrome": "Orphanet:3292", "Genetic vitreous-retinal disease": "Orphanet:98657", "pregnenolone sulfate {http": "CHEBI:35420", "Patella aplasia/hypoplasia": "Orphanet:86789", "M0 distant metastasis stage": "EFO:0004929", "lumbar disc herniation": "EFO:1002005", "KLHL9-related childhood-onset distal myopathy": "Orphanet:399081", "descending colon": "UBERON:0001158", "416B {http": "EFO:0005482", "Disorder of protein O-glycosylation": "Orphanet:309447", "non-alcoholic fatty liver disease severity measurement": "EFO:0008421", "G142": "EFO:0006405", "digestive system neoplasm": "EFO:0008549", "RNAtag-Seq": "EFO:0008897", "LP.07 seven leaves visible stage": "PO:0007063", "Lethal encephalopathy due to mitochondrial and peroxisomal fission defect": "Orphanet:330050", "Beta-thalassemia and related diseases": "Orphanet:275749", "response to gases and fumes exposure": "EFO:0006994", "Precancerous lesion of palpebral epidermis": "Orphanet:98583", "10X sequencing": "EFO:0008995", "CD4-negative, CD8-negative type I NK T cell secreting interferon-gamma": "CL:0000929", "triazolam": "CHEBI:9674", "Adult polyglucosan body disease": "Orphanet:206583", "NCI-H2172": "EFO:0006675", "Glycogen Storage Disease Type 2b": "EFO:1001333", "degree celsius": "UO:0000027", "fibroblast": "CL:0000057", "pigmented villonodular synovitis": "EFO:1001106", "Genetic acrokeratoderma": "Orphanet:183441", "response to statin": "GO:0036273", "animal body part": "EFO:0000808", "Trichodysplasia - xeroderma": "Orphanet:3361", "acylcarnitine measurement": "EFO:0005059", "circadian sleep/wake cycle, REM sleep": "GO:0042747", "Blepharo-cheilo-odontic syndrome": "Orphanet:1997", "Von Willebrand disease type 2": "Orphanet:166081", "diarsenic trioxide": "CHEBI:30621", "BS-Seq": "EFO:0008665", "Thymoma Type AB": "EFO:1000582", "leukocyte immunoglobulin-like receptor subfamily B member 1 measurement": "EFO:0008208", "parietal cortex measurement": "EFO:0008420", "urinary metabolite measurement": "EFO:0005116", "X-linked distal arthrogryposis multiplex congenita": "Orphanet:1145", "Crassostrea gigas": "NCBITaxon:29159", "triglyceride homeostasis": "EFO:0005881", "eyeball of camera-type eye": "UBERON:0010230", "GM12760": "EFO:0001151", "follicular thyroid adenoma": "EFO:0000499", "milligram per kilogram": "EFO:0002902", "Rorippa amphibia": "NCBITaxon:65951", "G4 ChIP-seq": "EFO:0008750", "Beckwith-Wiedemann syndrome due to NSD1 mutation": "Orphanet:238613", "Pyridoxine-dependent epilepsy": "Orphanet:3006", "Dacryocystitis - osteopoikilosis": "Orphanet:1562", "2q33.1 microdeletion syndrome": "Orphanet:251028", "Cymbidium ringspot virus": "NCBITaxon:12144", "Taeniopygia guttata": "NCBITaxon:59729", "Aspergillus multicolor": "NCBITaxon:41759", "docosadienoate {http": "CHEBI:78894", "Leishmania chagasi": "NCBITaxon:44271", "CS57843": "EFO:0000142", "S-[2,3-bis(palmitoyloxy)propyl]-Cys-Ser-Lys-Lys-Lys-Lys": "CHEBI:46889", "SU-DHL-2": "EFO:0007611", "GM17254 {http": "CLO:0014390", "1-methylnicotinamide {http": "CHEBI:16797", "Erythrokeratoderma variabilis progressiva": "Orphanet:308166", "Absent thumb - short stature - immunodeficiency": "Orphanet:2951", "Lymphedema": "Orphanet:79383", "secondary progressive multiple sclerosis": "EFO:0008522", "Proteus infectious disease": "EFO:1001130", "thioacetamide": "CHEBI:32497", "Syndrome with disorder of sex development of gynecological interest": "Orphanet:325638", "Karpas 422": "EFO:0005719", "alpha-beta intraepithelial T cell": "CL:0000797", "DF5018": "EFO:0004069", "Congenital laryngomalacia": "Orphanet:2373", "Sickle cell anemia": "Orphanet:232", "RNA-seq of non coding RNA from single cells": "EFO:0005685", "Primary immunodeficiency": "Orphanet:101997", "Cone dystrophy with supernormal rod response": "Orphanet:209932", "heart failure": "EFO:0003144", "IGA glomerulonephritis": "EFO:0004194", "skeletal muscle organ": "UBERON:0014892", "BJABK3": "EFO:0001090", "Mus musculus castaneus": "NCBITaxon:10091", "10x sequencing protocol": "EFO:0008443", "response to 5-fluoro-2'-deoxyuridine": "GO:0097330", "Hip dysplasia, Beukes type": "Orphanet:2114", "Zygodactyly type 1": "Orphanet:295187", "IMAGe syndrome": "Orphanet:85173", "Cleome gynandra": "NCBITaxon:190802", "Proximal renal tubular acidosis": "Orphanet:47159", "thymic macrophage": "CL:0000866", "Opitz G/BBB syndrome": "Orphanet:2745", "Preaxial polydactyly of toes, bilateral": "Orphanet:295177", "pemphigus erythematosus": "EFO:0008603", "Lipoid proteinosis": "Orphanet:530", "Botrytis cinerea {http": "NCBITaxon:40559", "Constriction rings syndrome": "Orphanet:295000", "Congenital nephrotic syndrome, Finnish type": "Orphanet:839", "Secondary entropion": "Orphanet:98569", "Autosomal dominant macrothrombocytopenia": "Orphanet:140957", "Distal myopathy, Nonaka type": "Orphanet:602", "nitrate": "CHEBI:17632", "Thin upper lip vermilion {http": "HP:0000219", "Xq12-q13.3 duplication syndrome": "Orphanet:314389", "hepatoma cell line": "EFO:0005216", "Distal monosomy 5q": "Orphanet:1627", "Papillary Craniopharyngioma": "EFO:1000447", "OS-Seq": "EFO:0008839", "mouth": "UBERON:0000165", "Keratoderma hereditarium mutilans": "Orphanet:494", "mandibular lateral line neuromast": "UBERON:2000125", "thoracic aortic raised atherosclerotic lesion": "EFO:0005618", "eosinophil progenitor cell": "CL:0000611", "femtomolar": "UO:0000073", "Familial hypospadias": "Orphanet:440", "Qualitative or quantitative defects of caveolin-3": "Orphanet:207078", "floor plate": "UBERON:0003079", "Bamforth-Lazarus syndrome": "Orphanet:1226", "fatty acid {http": "CHEBI:35366", "bundle branch block": "EFO:0004138", "dysmenorrheic pain measurement": "EFO:0007889", "GM14507 {http": "CLO:0031517", "shoot axis {http": "PO:0025029", "childhood acute myeloid leukemia with maturation": "EFO:1001945", "Short stature-optic atrophy-Pelger-Hu\u00c3\u00abt anomaly syndrome": "Orphanet:391677", "Amphiura filiformis": "NCBITaxon:82378", "Heterocephalus glaber": "NCBITaxon:10181", "ssRNA-seq": "EFO:0008950", "synapse part": "GO:0044456", "lymphoid tissue": "UBERON:0001744", "Hypertelorism-preauricular sinus-punctual pits-deafness syndrome": "Orphanet:293958", "Detroit562": "EFO:0002170", "Robinow syndrome": "Orphanet:97360", "Partial duplication of chromosome X": "Orphanet:263768", "Branchiostoma belcheri": "NCBITaxon:7741", "peer review quality control role": "EFO:0004447", "antilipemic drug": "CHEBI:35679", "embryonic day 17.5": "EFO:0002568", "rosiglitazone": "CHEBI:50122", "brown adipose tissue": "UBERON:0001348", "susceptibility to infectious disease measurement": "EFO:0008422", "Thoracolumbar scoliosis {http": "HP:0002944", "T1080": "EFO:0007608", "Prader-Willi syndrome due to paternal 15q11q13 deletion": "Orphanet:98793", "Homozygous 2p21 microdeletion syndrome": "Orphanet:369886", "Dystrophic epidermolysis bullosa": "Orphanet:303", "ALG13-CDG": "Orphanet:324422", "fear of severe pain measurement": "EFO:0008338", "fetal thymocyte": "CL:0002404", "clinical and behavioural ideal cardiovascular health": "EFO:0007654", "Sprague Dawley": "EFO:0001352", "stress-induced anxiety-like behavior": "EFO:1001920", "NCI-H2110": "EFO:0006673", "Epidermolytic ichthyosis": "Orphanet:312", "kidney": "UBERON:0002113", "Familial transthyretin-related amyloidosis": "Orphanet:271861", "ribonucleotide biosynthetic process": "GO:0009260", "homogenizer": "OBI:0400109", "cerebral cortex": "UBERON:0000956", "Cleft palate - short stature - vertebral anomalies": "Orphanet:2015", "Familial dilated cardiomyopathy": "Orphanet:217607", "GM14583 {http": "CLO:0031665", "Arthrogryposis - hyperkeratosis, lethal form": "Orphanet:1485", "Smart-Seq": "EFO:0008930", "Amaurosis - hypertrichosis": "Orphanet:1021", "Isolated congenital digital clubbing": "Orphanet:217059", "abnormality of temperature regulation": "HP:0004370", "PC-9": "EFO:0002847", "Sodium channelopathy-related small fiber neuropathy": "Orphanet:306577", "O-palmitoylcarnitine {http": "CHEBI:73067", "spine bone mineral density": "EFO:0007701", "Lumbosacral spina bifida cystica": "Orphanet:268758", "anisakiasis": "EFO:0007146", "Genetic cardiac tumor": "Orphanet:271841", "hatching gland": "UBERON:0002538", "high density lipoprotein particle size measurement": "EFO:0008592", "Abnormality of ion homeostasis": "HP:0003111", "Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes": "Orphanet:93216", "Kc": "EFO:0002068", "FAST-iCLIP": "EFO:0008737", "cambium {http": "PO:0005597", "Eyelashes hypertrophy": "Orphanet:98597", "Askin Tumor": "EFO:1000095", "small cell sarcoma": "EFO:1001184", "PAR-CLIP": "EFO:0008845", "volume percent": "UO:0000165", "Protein R deficiency": "Orphanet:2967", "X-linked neurodegenerative syndrome, Hamel type": "Orphanet:85336", "dengue disease": "EFO:0005547", "prostate intraepithelial neoplasia": "EFO:0002621", "pectoral fin cartilage": "ZFA:0000257", "Pulmonary arterial hypertension associated with congenital heart disease": "EFO:0009054", "COV434": "EFO:0006384", "COV504": "EFO:0006385", "carotene metabolic process": "GO:0016119", "conversion protocol": "EFO:0005520", "Humero-ulnar synostosis, unilateral": "Orphanet:295213", "phytohormone": "CHEBI:26158", "sodium pyruvate": "CHEBI:50144", "Familial medullary thyroid carcinoma": "Orphanet:99361", "otosclerosis": "EFO:0004213", "melanophage": "CL:0002060", "NCI-H1915": "EFO:0006666", "Autosomal recessive Kenny-Caffey syndrome": "Orphanet:93324", "hydroponic plant culture media": "EO:0007067", "Distal trisomy 17q": "Orphanet:3379", "facial height measurement": "EFO:0007856", "embryonic stage 13": "EFO:0005873", "physical activity": "EFO:0003940", "Autosomal recessive congenital cerebellar ataxia": "Orphanet:98095", "ficolin-1 measurement": "EFO:0008134", "Dopa-responsive dystonia": "Orphanet:255", "Syngnathia - cleft palate": "Orphanet:3263", "blood osmolality measurement": "EFO:0007967", "Pepper mild mottle virus": "NCBITaxon:12239", "Okajima": "EFO:0006715", "thioredoxin domain-containing protein 12 measurement": "EFO:0008298", "Rare hypolipidemia": "Orphanet:181431", "GM17211 {http": "CLO:0013890", "hair follicle": "UBERON:0002073", "Hermansky-Pudlak syndrome with neutropenia": "Orphanet:183678", "Acetobacter aceti": "NCBITaxon:435", "perhexiline": "CHEBI:35553", "Proteus-like syndrome": "Orphanet:2969", "Central polydactyly of fingers, unilateral": "Orphanet:295171", "TERV-ST": "EFO:0001251", "Lactobacillus mindensis": "NCBITaxon:167481", "Lu130": "EFO:0003142", "GM17161 {http": "CLO:0013982", "metaphysis of femur {http": "UBERON:0006865", "Mosaic trisomy 15": "Orphanet:1706", "parasympathetic nervous system": "UBERON:0000011", "extracellular space of host": "GO:0043655", "Autosomal recessive limb-girdle muscular dystrophy type 2D": "Orphanet:62", "dermatomyositis": "EFO:0000398", "Isolated aniridia": "Orphanet:250923", "colorectum": "UBERON:0012652", "143B": "EFO:0006355", "SAPAS": "EFO:0008902", "X-linked recessive intellectual disability - macrocephaly - ciliary dysfunction": "Orphanet:83648", "Angiofibroma": "EFO:1001761", "Colon Neuroendocrine Tumor G1": "EFO:1000188", "macromolecule metabolic process": "GO:0043170", "Spinocerebellar ataxia type 37": "Orphanet:363710", "Mycobacterium bovis": "NCBITaxon:1765", "2,3-bis(4-hydroxyphenyl)propionitrile": "CHEBI:63949", "AA87": "EFO:0004026", "gastrula 50%-epiboly": "EFO:0001291", "CB678": "EFO:0004050", "CD11b-high, CD103-negative, langerin-negative lymph node dendritic cell": "CL:0002512", "organism status design": "EFO:0001751", "Hypomyelination - congenital cataract": "Orphanet:85163", "brain hypoxia-Ischemia": "EFO:1000846", "Methylmalonic acidemia with homocystinuria type cblF": "Orphanet:79284", "Congenital muscular dystrophy, Ullrich type": "Orphanet:75840", "Cutis gyrata - acanthosis nigricans - craniosynostosis": "Orphanet:1555", "Haloferax volcanii": "NCBITaxon:2246", "GM17828 {http": "CLO:0016521", "Syndromic corneal dystrophy": "Orphanet:98628", "Ovarian Dysgerminoma": "EFO:1000414", "Hypertelorism - hypospadias - polysyndactyly syndrome": "Orphanet:2211", "Mosaic trisomy 12": "Orphanet:1698", "Y chromosome number anomaly": "Orphanet:263746", "technology type": "EFO:0005521", "embryonic leading edge cell": "FBbt:00005746", "1-myristoyl-2-palmitoyl-sn-glycero-3-phosphocholine {http": "CHEBI:75062", "Spondyloepiphyseal dysplasia, Reardon type": "Orphanet:163662", "extracellular matrix protein 1 measurement": "EFO:0008126", "mesoderm": "UBERON:0000926", "Rhagoletis pomonella": "NCBITaxon:28610", "system development": "GO:0048731", "Disorder of phospholipids, sphingolipids and fatty acids biosynthesis": "Orphanet:352301", "Micro-C XL": "EFO:0008808", "extraversion": "EFO:0004317", "CAST/EiJ": "EFO:0007727", "Methanococcus maripaludis": "NCBITaxon:39152", "neurogenic placode": "UBERON:0009955", "Testicular Sertoli Cell Tumor": "EFO:1000572", "hypocotyl emergence stage": "PO:0007043", "Heschl's gyrus morphology measurement": "EFO:0005852", "alpha-adrenergic agonist": "CHEBI:35569", "Rare hereditary systemic disease with peripheral neuropathy": "Orphanet:207021", "REM sleep behavior disorder": "EFO:0007462", "process quality": "PATO:0001236", "Trichoplax adhaerens": "NCBITaxon:10228", "basophilic metamyelocyte": "CL:0000769", "blastula sphere": "EFO:0001283", "response to rate control therapy": "EFO:0005768", "tongue neoplasm": "EFO:0003871", "Autosomal recessive optic atrophy, OPA6 type": "Orphanet:99012", "Intellectual disability, Birk-Barel type": "Orphanet:166108", "recombinant inbred strain": "EFO:0004008", "CREST-seq": "EFO:0008700", "granzyme A measurement": "EFO:0008145", "SH-SY5Y": "EFO:0002717", "RAD": "EFO:0008878", "Intellectual disability - hypotonia - skin hyperpigmentation": "Orphanet:3050", "rhombomere 3 floor plate": "UBERON:0005573", "CD8-Positive T-Lymphocytes": "EFO:0004219", "Trichomonas vaginalis": "NCBITaxon:5722", "tempol": "EFO:0002678", "Caulobacter vibrioides": "NCBITaxon:155892", "Adenomyosis": "EFO:1001757", "Aptenodytes patagonicus": "NCBITaxon:9234", "Severe combined immunodeficiency": "Orphanet:183660", "cytokinins": "CHEBI:23530", "Plasmodium vivax": "NCBITaxon:5855", "non-typhoidal Salmonella bacteremia": "EFO:0009087", "eicosapentaenoic acid measurement": "EFO:0007760", "Myelofibrosis {http": "HP:0011974", "vascular tissue": "PO:0009015", "Coronatine {http": "CHEBI:80730", "Retinal vasculopathy and cerebral leukodystrophy": "Orphanet:247691", "Conjunctival vascular anomaly": "Orphanet:98611", "salivary gland squamous cell carcinoma": "EFO:1001967", "base metabolic rate measurement": "EFO:0007777", "Leukoencephalopathy - metaphyseal chondrodysplasia": "Orphanet:83629", "SJRH30": "EFO:0002329", "CD4-negative CD8-negative gamma-delta intraepithelial T cell": "CL:0000803", "acute respiratory distress syndrome": "EFO:1000637", "Hereditary neurocutaneous angioma": "Orphanet:1062", "Craniosynostosis, Boston type": "Orphanet:1541", "Primary pigmented nodular adrenocortical disease": "Orphanet:189439", "molar-incisor hypomineralization": "EFO:0005321", "Genetic dermis disorder": "Orphanet:183472", "Hepatoerythropoietic porphyria": "Orphanet:95159", "46,XX disorder of sex development induced by fetoplacental androgens excess": "Orphanet:325061", "CS57873": "EFO:0000152", "Renal hypoplasia": "Orphanet:93101", "Meningomyelocele": "EFO:1001369", "Other immunodeficiency syndromes due to defects in innate immunity": "Orphanet:331193", "petal {http": "PO:0009032", "Classical phenylketonuria": "Orphanet:79254", "Escherichia coli": "NCBITaxon:562", "mucinous carcinoma": "EFO:0000197", "SKMES1": "EFO:0002334", "Congenital primary aphakia": "Orphanet:83461", "ATP biosynthetic process": "GO:0006754", "Glutaryl-CoA dehydrogenase deficiency": "Orphanet:25", "Spondyloepimetaphyseal dysplasia, Genevi\u00c3\u00a8ve type": "Orphanet:168454", "Scalp defects - postaxial polydactyly": "Orphanet:1003", "epithelial neoplasm": "EFO:0006858", "neurogenic locus notch homolog protein 1 measurement": "EFO:0008246", "caudal division of the internal carotid artery": "UBERON:2001051", "Brassica carinata": "NCBITaxon:52824", "isoflurane": "CHEBI:6015", "CNS hypomyelination {http": "HP:0003429", "Lassa virus Josiah": "NCBITaxon:11622", "Behavioral variant of frontotemporal dementia": "Orphanet:275864", "traffic air pollution measurement": "EFO:0007908", "hMeDIP-seq": "EFO:0008767", "De Quervain disease": "EFO:1000891", "Hereditary cerebral hemorrhage with amyloidosis": "Orphanet:85458", "quiescent center": "PO:0020149", "rhabdomyosarcoma": "EFO:0002918", "Paranasal Sinus Schneiderian Papilloma": "EFO:1000455", "Focal facial dermal dysplasia": "Orphanet:398166", "gamma-linolenate {http": "CHEBI:32391", "response to glucocorticoid": "GO:0051384", "Glycogen storage disease due to GLUT2 deficiency": "Orphanet:2088", "Intestinal epithelial dysplasia": "Orphanet:92050", "mesalamine": "CHEBI:6775", "Methylmalonic acidemia with homocystinuria, type cblC": "Orphanet:79282", "abnormality of the mouth": "HP:0000153", "Upper limb mesomelic dysplasia": "Orphanet:2497", "serotonin measurement": "EFO:0004846", "Charcot-Marie-Tooth disease type 1F": "Orphanet:101085", "Pituitary stalk interruption syndrome": "Orphanet:95496", "C-C motif chemokine 18 measurement": "EFO:0008046", "hybridization station": "OBI:0400111", "blood coagulation": "GO:0007596", "Holoprosencephaly": "Orphanet:2162", "CD8-positive, alpha-beta thymocyte": "CL:0000811", "Caenorhabditis elegans": "NCBITaxon:6239", "Mosaic genome-wide paternal uniparental disomy": "Orphanet:329813", "presumptive rhombomere 3": "UBERON:0007290", "Eye Foreign Bodies": "EFO:1001322", "SBC-3": "EFO:0002854", "Calyptogena pacifica gill symbiont": "NCBITaxon:72603", "Hypotrichosis - lymphedema - telangiectasia": "Orphanet:69735", "thrombopoietin": "EFO:0003236", "Rare hereditary disease with avascular necrosis": "Orphanet:399185", "Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma": "EFO:1000383", "Lethal ataxia with deafness and optic atrophy": "Orphanet:1187", "Neurofibromatosis-Noonan syndrome": "Orphanet:638", "secondary hypertrophic osteoarthropathy": "EFO:1001174", "environmental tobacco smoke exposure measurement": "EFO:0008361", "Distal trisomy 20q": "Orphanet:96107", "Trilogy of Fallot": "EFO:1001439", "somite 5": "UBERON:2000073", "Congenital non-bullous ichthyosiform erythroderma": "Orphanet:79394", "LX837": "EFO:0005489", "testicular dysgenesis syndrome": "EFO:0004893", "saline": "EFO:0002677", "mental or behavioural disorder biomarker": "EFO:0006848", "RHYNS syndrome": "Orphanet:140976", "SF539": "EFO:0005453", "response to mercaptopurine": "EFO:0007853", "Qualitative or quantitative defects of protein ZASP": "Orphanet:209050", "joule per square centimeter": "EFO:0004427", "Primary hyperoxaluria type 1": "Orphanet:93598", "Filamin-related bone disorder": "Orphanet:93425", "Caki2": "EFO:0002150", "childhood B acute lymphoblastic leukemia": "EFO:1001946", "flagellin": "EFO:0003241", "columella root cap cell {http": "PO:0020132", "Disorder of pentose phosphate metabolism": "Orphanet:79186", "microbiome": "EFO:0004982", "Isolated ankyloblepharon filiforme adnatum": "Orphanet:91397", "Familial papillary or follicular thyroid carcinoma": "Orphanet:319487", "Lactobacillus delbrueckii": "NCBITaxon:1584", "Syracuse High Avoidance": "EFO:0001346", "HCC1576": "EFO:0006429", "respiratory epithelial cell": "CL:0002368", "disopyramide": "CHEBI:4657", "Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency": "Orphanet:88639", "Hs 936.T": "EFO:0006594", "Ankyloblepharon filiforme adnatum - cleft palate": "Orphanet:1072", "CS57751": "EFO:0000086", "Partial deletion of the long arm of chromosome 3": "Orphanet:262019", "Peritoneal Well Differentiated Papillary Mesothelioma": "EFO:1000469", "Small Intestinal Enteropathy-Associated T-Cell Lymphoma": "EFO:1000535", "chronic inflammatory demyelinating polyradiculoneuropathy": "EFO:1000868", "Muscular hypotonia of the trunk {http": "HP:0008936", "Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome": "Orphanet:397623", "seminal fluid": "UBERON:0006530", "mating type h plus": "EFO:0004036", "testis": "UBERON:0000473", "bone mineral accretion measurement": "EFO:0007591", "cardiac mesoderm primordium": "EFO:0000315", "fractional excretion of magnesium measurement": "EFO:0008450", "GM17111 {http": "CLO:0014947", "pleurisy": "EFO:1001825", "CS57743": "EFO:0000084", "Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells": "Orphanet:169443", "endoderm": "UBERON:0000925", "amplicon sequencing": "EFO:0003747", "Aegilops speltoides {http": "NCBITaxon:4573", "2q32q33 microdeletion syndrome": "Orphanet:251019", "Karyomegalic interstitial nephritis": "Orphanet:401996", "Short stature due to partial GHR deficiency": "Orphanet:314802", "neurotic disorder": "EFO:0004257", "Hereditary stomatocytosis": "Orphanet:98365", "Partial deletion of the long arm of chromosome 14": "Orphanet:262110", "larval day 5": "EFO:0001305", "disease course": "OGMS:0000063", "PR interval": "EFO:0004462", "Vitis vinifera subsp. silvestris {http": "NCBITaxon:755351", "Multifocal epileptiform discharges {http": "HP:0010841", "GM17783 {http": "CLO:0016684", "Hypotrichosis with juvenile macular degeneration": "Orphanet:1573", "pars intercerebralis": "UBERON:0001059", "artery": "UBERON:0001637", "TERV-AntiSenseB56": "EFO:0001250", "Lactobacillus casei": "NCBITaxon:1582", "amyloidosis": "EFO:1001875", "iPS DF 19.7": "EFO:0007095", "muscle measurement": "EFO:0004515", "Partial trisomy of the long arm of chromosome 5": "Orphanet:262869", "Intellectual disability - myopathy - short stature - endocrine defect": "Orphanet:3068", "mucosa of tongue": "UBERON:0005020", "Desbuquois syndrome": "Orphanet:1425", "GM12156": "EFO:0001141", "Achalasia - microcephaly": "Orphanet:929", "Small Intestinal Diffuse Large B-Cell Lymphoma": "EFO:1000534", "Severe feeding difficulties - failure to thrive - microcephaly due to ASXL3 deficiency": "Orphanet:352577", "basal": "EFO:0001654", "Rubinstein-Taybi syndrome": "Orphanet:783", "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency": "Orphanet:95699", "2q31.1 microduplication syndrome": "Orphanet:294026", "dicrocoeliasis": "EFO:0007234", "inflorescence meristem {http": "PO:0000230", "diffuse lipomatosis": "EFO:1000687", "response to vancomycin": "EFO:0007647", "BC-5": "EFO:0002047", "Hydrocephalus {http": "HP:0000238", "LDL cholesterol change measurement": "EFO:0007804", "Blackfan-Diamond anemia": "Orphanet:124", "Apert syndrome": "Orphanet:87", "Autosomal dominant optic atrophy and peripheral neuropathy": "Orphanet:250932", "gastric cardia carcinoma": "EFO:1001252", "polymeric immunoglobulin receptor measurement": "EFO:0008267", "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia": "Orphanet:363972", "Pseudomonas aeruginosa CF5 infection": "EFO:0001077", "WHIM syndrome": "Orphanet:51636", "L-2-hydroxyglutaric aciduria": "Orphanet:79314", "eosinophilic metamyelocyte": "CL:0000773", "Arthrogryposis-like hand anomaly - sensorineural deafness": "Orphanet:1144", "non-dense area measurement": "EFO:0006504", "Trisomy 8p": "Orphanet:264450", "Dislocation of the hip - dysmorphism": "Orphanet:2412", "plant growth retardant": "CHEBI:35219", "Focal palmoplantar keratoderma": "Orphanet:307837", "Pongo abelii": "NCBITaxon:9601", "Desmosterolosis": "Orphanet:35107", "AB2.2": "EFO:0002812", "mating type alpha": "EFO:0001270", "N-isovalerylglycine {http": "CHEBI:70984", "Clostridium acetobutylicum ATCC 824": "NCBITaxon:272562", "cob": "ZEA:0015075", "far red light regimen": "EO:0007203", "parasitemia measurement": "EFO:0005528", "variant Creutzfeld Jacob disease": "EFO:0004597", "Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes": "Orphanet:357332", "Median nodule of the upper lip": "Orphanet:2699", "symmetric dimethylarginine": "CHEBI:25682", "Musculoskeletal disease with cataract": "Orphanet:98648", "X and Y chromosomal anomaly": "Orphanet:263749", "somite 2": "UBERON:2000728", "castasterone": "CHEBI:23051", "Hypocrea virens": "NCBITaxon:29875", "Greig cephalopolysyndactyly syndrome": "Orphanet:380", "Short rib dysplasia": "Orphanet:93426", "COLO201": "EFO:0002135", "embryonic stage 7": "EFO:0005866", "AR-C124910XX\u00c2\u00a0measurement": "EFO:0007020", "nitrogen compound metabolic process": "GO:0006807", "cleavage 16-cell": "EFO:0001284", "Tibial Adamantinoma": "EFO:1000596", "nervonic acid measurement": "EFO:0007977", "3alpha-hydroxy-5beta-pregnan-20-one {http": "CHEBI:1712", "Burkitt lymphoma cell": "BTO:0000164", "GRACILE syndrome": "Orphanet:53693", "Normal Human Astrocytes": "EFO:0002777", "cardiac myocyte cell derived cell line": "EFO:0005731", "Central Nervous System Anaplastic Large Cell Lymphoma": "EFO:1000156", "Cerebellar Liponeurocytoma": "EFO:1000159", "fungal cell": "CL:0000521", "Intellectual disability - craniofacial dysmorphism - cryptorchidism": "Orphanet:329224", "Autosomal dominant childhood-onset proximal spinal muscular atrophy": "Orphanet:363447", "SK-N-AS": "EFO:0002859", "stele {http": "PO:0025197", "stomach rupture": "EFO:1001851", "strain": "EFO:0005135", "oviduct": "UBERON:0000993", "response to cytokine": "GO:0034097", "Genetic renal tubular disease": "Orphanet:183592", "mast-cell leukemia": "EFO:0007359", "Autosomal recessive secondary polycythemia not associated with VHL gene": "Orphanet:247378", "Subacute Combined Degeneration": "EFO:1001428", "Infantile Refsum disease": "Orphanet:772", "Epiphyseal dysplasia - hearing loss - dysmorphism": "Orphanet:1825", "nucleoside triphosphate biosynthetic process": "GO:0009142", "KU812": "EFO:0002222", "diploid cell": "CL:0000415", "Autism spectrum disorder due to AUTS2 deficiency": "Orphanet:352490", "Taussig-Bing syndrome": "Orphanet:101042", "Pelvic Inflammatory Disease": "EFO:1001388", "Epilepsy and/or ataxia with myoclonus as major feature": "Orphanet:306756", "Insulin-resistance syndrome type B": "Orphanet:2298", "spiracle": "UBERON:6005054", "Congenital chronic diarrhea with protein-losing enteropathy": "Orphanet:329242", "vulva fibroepithelial polyp": "EFO:1000777", "Spastic tetraplegia - retinitis pigmentosa - intellectual disability": "Orphanet:3011", "Isolated glycerol kinase deficiency": "Orphanet:408", "acute kidney tubular necrosis": "EFO:1000794", "HSD10 disease, infantile type": "Orphanet:391428", "CD24-negative CD38-negative IgG-negative class switched memory B cell": "CL:0002121", "Cavernous hemangiomas of face - supraumbilical midline raphe": "Orphanet:2124", "ND01173 {http": "CLO:0028397", "ehrlich tumor carcinoma": "EFO:1000913", "cystic liver disease": "EFO:1001505", "thermal cycler": "OBI:0400116", "arcus senilis": "EFO:1000818", "presumptive forebrain midbrain boundary": "UBERON:0007288", "Partial deletion of chromosome X": "Orphanet:263726", "Thickened earlobes - conductive deafness": "Orphanet:2405", "retinoblastoma (nonhereditary)": "EFO:0005717", "Genetic gynecological tumor": "Orphanet:183734", "Populus maximowiczii x Populus nigra": "NCBITaxon:343990", "Illumina Genome Analyzer II": "EFO:0004201", "plexin-C1 measurement": "EFO:0008266", "time": "EFO:0000721", "seroconversion": "EFO:0007851", "Familial hyperaldosteronism type III": "Orphanet:251274", "ATC Code M Musculo-skeletal system": "EFO:0005642", "Myostatin-related muscle hypertrophy": "Orphanet:275534", "ephrin type-B receptor 2 measurement": "EFO:0008124", "Disorder of sex development - intellectual disability": "Orphanet:2983", "Pan troglodytes troglodytes": "NCBITaxon:37011", "ST3GAL5-CDG": "Orphanet:370933", "nicotine metabolite ratio": "EFO:0007794", "comprehensive strength index": "EFO:0004979", "STRT": "EFO:0008953", "presumptive midbrain hindbrain boundary": "UBERON:0007281", "Congenital lactase deficiency": "Orphanet:53690", "Pancreatic Small Cell Neuroendocrine Carcinoma": "EFO:1000444", "maxillary sinusitis": "EFO:0007361", "visual acuity measurement": "EFO:0008385", "Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis": "Orphanet:93213", "Hereditary vascular retinopathy": "Orphanet:71291", "nutritional deficiency disease": "EFO:1001067", "exposure temperature": "EFO:0000718", "Eyebrow duplication - syndactyly": "Orphanet:3172", "Benign Kidney Neoplasm": "EFO:1000111", "Isolated thyrotropin-releasing hormone deficiency": "Orphanet:238670", "oral leukoedema": "EFO:1001075", "Pyruvate dehydrogenase E1-beta deficiency": "Orphanet:255138", "Genetic cranial malformation": "Orphanet:183542", "CS57622": "EFO:0000039", "MORM syndrome": "Orphanet:75858", "Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form": "Orphanet:308684", "entopterygoid": "UBERON:2000657", "GM17149 {http": "CLO:0013947", "ILSXISS26/TejJ": "EFO:0002982", "Teleopsis whitei": "NCBITaxon:139651", "Complex chromosomal rearrangement": "Orphanet:263708", "X-linked mandibulofacial dysostosis": "Orphanet:1131", "Autosomal dominant focal dystonia, DYT25": "Orphanet:329466", "endophenotype": "EFO:0006988", "dentate gyrus of hippocampal formation {http": "UBERON:0001885", "gSELEX-Seq": "EFO:0008757", "clone end sequencing": "EFO:0003743", "Ehlers-Danlos syndrome, vascular-like type": "Orphanet:230845", "OV90": "EFO:0002311", "Ck-beta-8-1 measurement": "EFO:0008085", "CirSeq": "EFO:0008691", "Hypocrea jecorina": "NCBITaxon:51453", "Jiyoye": "EFO:0002215", "central neurocytoma": "EFO:1000856", "sensory perception of sound": "GO:0007605", "tetrafluoroethene": "CHEBI:38866", "high content analysis of cells": "EFO:0005397", "molluscum contagiosum": "EFO:0007375", "Eubalaena glacialis": "NCBITaxon:27606", "pyelitis": "EFO:1001140", "Autosomal recessive spastic paraplegia type 57": "EFO:0009017", "systemic scleroderma": "EFO:0000717", "CGP 78608 hydrochloride": "CHEBI:64065", "Episodic ataxia type 6": "Orphanet:209967", "ilium": "UBERON:0001273", "cyclosporiasis": "EFO:0007230", "Proximal myopathy with extrapyramidal signs": "Orphanet:401768", "Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism": "Orphanet:280679", "Neuronal intranuclear inclusion disease": "Orphanet:2289", "Familial partial epilepsy": "Orphanet:309", "Late infantile neuronal ceroid lipofuscinosis": "Orphanet:168491", "Scott syndrome": "Orphanet:806", "Arterivirus infectious disease": "EFO:0007152", "hilar portion of hepatic duct": "UBERON:0015423", "receptive language perception": "EFO:0005686", "maximal midexpiratory flow rate": "EFO:0004313", "Autosomal dominant spastic paraplegia type 9": "Orphanet:100990", "Focal, segmental or multifocal dystonia": "Orphanet:1866", "Thoraco-abdominal enteric duplication": "Orphanet:1759", "central memory CD4-positive, alpha-beta T cell": "CL:0000904", "Occipital encephalocele": "Orphanet:268823", "lipid pneumonia": "EFO:0007345", "proctitis": "EFO:0005628", "LDL peak particle diameter measurement": "EFO:0007677", "Cafe-au-lait spot {http": "HP:0000957", "Duane retraction syndrome": "Orphanet:233", "myxothiazol": "CHEBI:25461", "Partial duplication of the long arm of chromosome 6": "Orphanet:262878", "rickettsiosis": "EFO:1001162", "Freeman-Sheldon syndrome": "Orphanet:2053", "Benign non-familial infantile seizures": "Orphanet:166295", "resveratrol": "CHEBI:27881", "Cole-Carpenter syndrome": "Orphanet:2050", "CaHPV10": "EFO:0002147", "calcium oxalate urolithiasis": "EFO:0009065", "Autosomal recessive limb-girdle muscular dystrophy": "Orphanet:102015", "pneumonitis": "EFO:1001991", "Qualitative or quantitative defects of alpha-actin": "Orphanet:209059", "ILSXISS94/TejJ": "EFO:0002999", "caffeine": "CHEBI:27732", "biomaterial provider": "EFO:0001729", "Polistes metricus": "NCBITaxon:91422", "hyaluronan": "CHEBI:16336", "bicalutamide": "CHEBI:3090", "fat cell": "CL:0000136", "Populus nigra": "NCBITaxon:3691", "Growth hormone insensitivity syndrome": "Orphanet:181393", "schizophrenia symptom severity measurement": "EFO:0007927", "HUES13": "EFO:0007078", "CS57859": "EFO:0000148", "Equus caballus": "NCBITaxon:9796", "orotate {http": "CHEBI:30839", "Infantile hypercalcemia {http": "HP:0008250", "Hashimoto's thyroiditis": "EFO:0003779", "gastrula 90%-epiboly": "EFO:0001293", "Spodoptera frugiperda": "NCBITaxon:7108", "Parotid Gland Carcinoma ex Pleomorphic Adenoma": "EFO:1000461", "vascular endothelial growth factor receptor 2 measurement": "EFO:0008314", "Femur-fibula-ulna complex": "Orphanet:2019", "QGP-1": "EFO:0006741", "Lethal omphalocele-cleft palate syndrome": "Orphanet:2736", "longitudinal visceral muscle primordium": "FBbt:00017008", "Maternal 14q32.2 microdeletion syndrome": "Orphanet:254528", "micrometer": "UO:0000017", "Hypobetalipoproteinemia": "Orphanet:31154", "MYH9-related disease": "Orphanet:182050", "True unicornuate uterus": "Orphanet:180074", "citrate(1-) {http": "CHEBI:35804", "Autosomal recessive hyperinsulinism due to Kir6.2 deficiency": "Orphanet:79644", "Congenital hereditary endothelial dystrophy type I": "Orphanet:98975", "Uk-3": "EFO:0005163", "ribonucleoside triphosphate metabolic process": "GO:0009199", "childhood T lymphoblastic lymphoma": "EFO:1001948", "Nasal Septal Perforation": "EFO:1001813", "Pustulosis palmaris et plantaris": "Orphanet:163927", "PARTE": "EFO:0008849", "pericardial fat": "UBERON:0035814", "Casuarina glauca": "NCBITaxon:3522", "Distal monosomy 12p": "Orphanet:280325", "X-linked intellectual disability - hypogammaglobulinemia - progressive neurological deterioration": "Orphanet:85317", "Listeria monocytogenes EGD-e": "NCBITaxon:169963", "estrogen receptor antagonist role": "CHEBI:50792", "chest": "UBERON:0001443", "acute myeloid leukemia": "EFO:0000222", "smooth muscle cell derived cell line": "EFO:0005735", "gastric antral vascular ectasia": "EFO:1000945", "potassium dichromate": "CHEBI:53444", "Endometrial Small Cell Carcinoma": "EFO:1000239", "idiopathic cardiomyopathy": "EFO:0000767", "pseudomyxoma peritonei": "EFO:0007456", "forebrain": "UBERON:0001890", "salivary gland disease": "EFO:0008581", "Pancytopenia-developmental delay syndrome": "Orphanet:401764", "CS57850": "EFO:0000145", "N-acetyl-L-methionine {http": "CHEBI:21557", "alpha-tocopherol measurement": "EFO:0007898", "Capan2": "EFO:0002154", "morphine dependence": "EFO:0005612", "Streptomyces hygroscopicus subsp. jinggangensis": "NCBITaxon:311982", "Acro-pectoro-renal dysplasia": "Orphanet:956", "Neurodegeneration with brain iron accumulation": "Orphanet:385", "breast cyst": "EFO:1000848", "Progressive visual loss {http": "HP:0000529", "2,2'-bipyridine": "CHEBI:30351", "anogenital venereal wart": "EFO:0007147", "Hemimelia": "Orphanet:2130", "B-1 B cell": "CL:0000819", "Atypical hemolytic-uremic syndrome with anti-factor H antibodies": "Orphanet:93581", "germ ring": "UBERON:0002541", "cellulitis": "EFO:0003035", "babesiosis": "EFO:0007162", "Ascher syndrome": "Orphanet:1253", "Autosomal recessive distal myopathy": "Orphanet:206653", "nucleic acid hybridization to array protocol": "EFO:0003815", "Embolism, Paradoxical": "EFO:1001308", "N-acetyl-L-serine {http": "CHEBI:45441", "isoniazide": "CHEBI:6030", "So-Eum": "EFO:0007123", "CD8_alpha-negative plasmactyoid dendritic cell": "CL:0002455", "Partial duplication of the long arm of chromosome 7": "Orphanet:262887", "T24": "EFO:0002864", "anterior endoderm primordium": "EFO:0000261", "Abnormality of urine homeostasis": "HP:0003110", "Lewy body dementia": "EFO:0006792", "Non-dystrophic myopathy with collagen 6 anomaly": "Orphanet:206659", "Alexander disease": "Orphanet:58", "Abnormality of head or neck": "HP:0000152", "response to dabigatran etexilate": "EFO:0005205", "asbestosis": "EFO:0007153", "Heliconius erato etylus x Heliconius himera": "NCBITaxon:529916", "Mandibulofacial dysostosis": "Orphanet:155899", "denture stomatitis": "EFO:1000893", "Prader-Willi syndrome due to point mutation": "Orphanet:398069", "Impaired social interactions {http": "HP:0000735", "Dyggve-Melchior-Clausen disease": "Orphanet:239", "gastric adenosquamous carcinoma": "EFO:1000029", "ILSXISS16/TejJ": "EFO:0002976", "G1E-ER4": "EFO:0002055", "Cryptococcus neoformans": "NCBITaxon:5207", "sodium tungstate": "CHEBI:63940", "SK-CO-1": "EFO:0006752", "maxillary sinus neoplasm": "EFO:1001035", "brain structure developmental tissue": "EFO:0001910", "Ulnar hemimelia": "Orphanet:93320", "Femoral-facial syndrome": "Orphanet:1988", "cholinesterase inhibitor": "CHEBI:37733", "MHH-NB-11": "EFO:0006651", "8-(3-chlorostyryl) caffeine": "CHEBI:53115", "emphysema imaging measurement": "EFO:0007626", "clear cell": "EFO:0003036", "Incontinentia pigmenti": "Orphanet:464", "O-stearoylcarnitine {http": "CHEBI:73074", "Colorectal Adenosquamous Carcinoma": "EFO:1000190", "Gaucher disease": "Orphanet:355", "Stern-Lubinsky-Durrie syndrome": "Orphanet:3194", "RICC-seq": "EFO:0008894", "thoracic segment of trunk": "UBERON:0000915", "mature CD11c-low plasmacytoid dendritic cell": "CL:0000993", "48,XXYY syndrome": "Orphanet:10", "epilepsy with generalized tonic-clonic seizures": "EFO:0007262", "Campomelia, Cumming type": "Orphanet:1318", "Vitreoretinopathy": "Orphanet:98668", "Abnormality of phosphate homeostasis": "HP:0100529", "Partial duplication of chromosome 1": "Orphanet:262191", "Cytomegalic congenital adrenal hypoplasia": "Orphanet:95702", "decubitus ulcer": "EFO:0007067", "Monilethrix": "Orphanet:573", "Factor XIII subunit A deficiency": "HP:0040233", "Penile Fibromatosis": "EFO:1000466", "8p23.1 microdeletion syndrome": "Orphanet:251071", "ARS-Seq": "EFO:0008653", "5q31.3 microdeletion syndrome": "Orphanet:314655", "butyrylcholinesterase measurement": "EFO:0004571", "transcriptome": "EFO:0004421", "CD38-negative immature B cell": "CL:0002055", "Distal hereditary motor neuropathy type 2": "Orphanet:139525", "spotted single stranded DNA PCR amplicon reporter": "EFO:0005078", "TR389": "EFO:0004060", "ventral imaginal precursor": "FBbt:00005834", "DNA selection through 5-methylcytidine antibody": "EFO:0004180", "tyrosine": "CHEBI:18186", "Neonatal hemochromatosis": "Orphanet:446", "Monosomy 22": "Orphanet:96123", "ganglion": "UBERON:0000045", "Partial deletion of the long arm of chromosome 5": "Orphanet:262038", "Disorder of carbohydrate absorption and transport": "Orphanet:309001", "TYK-nu": "EFO:0006766", "OAW28": "EFO:0006704", "diaphragmatic eventration": "EFO:1000898", "GM07357": "EFO:0001116", "Generalized hypotonia {http": "HP:0001290", "Phakomatosis cesioflammea": "Orphanet:79483", "WSB/EiJ": "EFO:0007731", "Oryza punctata {http": "NCBITaxon:4537", "lung disease severity measurement": "EFO:0007744", "WEHI-231 cell": "BTO:0001093", "Distal anoctaminopathy": "Orphanet:399096", "somatic stem cell division": "GO:0048103", "lymphangiomyoma": "EFO:1001027", "natural killer cell activation": "GO:0030101", "atrial flutter": "EFO:0003911", "eye disease": "EFO:0003966", "Caldicellulosiruptor lactoaceticus": "NCBITaxon:52766", "peptic esophagitis": "EFO:1001095", "Leiomyoma, Epithelioid": "EFO:1001356", "Pigmented conjunctival lesion": "Orphanet:98615", "N-acetyltyrosine {http": "CHEBI:68561", "CS57544": "EFO:0000010", "follicular mucinosis": "EFO:1000701", "Pseudomonas stutzeri A1501": "NCBITaxon:379731", "Slamf1-positive multipotent progenitor cell": "CL:0002036", "1-palmitoleoyl-2-linoleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:84567", "kelvin": "UO:0000012", "adenosarcoma": "EFO:0007134", "N-acetyl-D-tryptophan {http": "CHEBI:16734", "Solanum chacoense": "NCBITaxon:4108", "Congenital cataracts - facial dysmorphism - neuropathy": "Orphanet:48431", "benign prostatic hyperplasia": "EFO:0000284", "Isolated Dandy-Walker malformation with hydrocephalus": "Orphanet:269212", "1,2-dibromoethane": "CHEBI:28534", "Ulnar hemimelia, bilateral": "Orphanet:295073", "RKO": "EFO:0001232", "Thomsen and Becker disease": "Orphanet:614", "susceptibility to mumps measurement": "EFO:0008404", "bronchogenic carcinoma": "EFO:1001942", "test result": "EFO:0000720", "Partial duplication of the short arm of chromosome 10": "Orphanet:262776", "DSBCapture": "EFO:0008725", "B140H": "EFO:0002042", "Genetic soft tissue tumor": "Orphanet:271832", "Autosomal dominant osteosclerosis, Worth type": "Orphanet:2790", "McLeod neuroacanthocytosis syndrome": "Orphanet:59306", "Hammer Toe Syndrome": "EFO:1001336", "arachidate {http": "CHEBI:32360", "Microcephalic primordial dwarfism, Alazami type": "Orphanet:319671", "C3H/HeJ": "EFO:0001329", "dendritic cell-derived osteoclast": "EFO:0002662", "Repli-Seq": "EFO:0008889", "response to abacavir": "EFO:0006905", "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness": "Orphanet:101097", "Wissler's syndrome": "EFO:0007547", "Hunter-McAlpine craniosynostosis": "Orphanet:97340", "foregut primordium": "FBbt:00005535", "Familial intrahepatic cholestasis": "Orphanet:284385", "Butyrivibrio proteoclasticus B316": "NCBITaxon:515622", "Cubital Tunnel Syndrome": "EFO:1001301", "sleep measurement": "EFO:0004870", "promonocyte": "CL:0000559", "Tibial hemimelia, bilateral": "Orphanet:295079", "Short rib-polydactyly syndrome, Beemer-Langer type": "Orphanet:93268", "AIDS related complex": "EFO:0007137", "hypopharyngeal carcinoma": "EFO:0002938", "solar lentigines measurement": "EFO:0007850", "chorion cell line": "EFO:0002781", "LP.06 six leaves visible stage": "PO:0007123", "Skin Sarcoma": "EFO:1000531", "Partial deletion of the long arm of chromosome 17": "Orphanet:262137", "spontaneous mutation": "EFO:0004018", "sulphur dioxide": "CHEBI:18422", "Gastric Papillary Adenocarcinoma": "EFO:1000276", "Familial cortical myoclonus": "Orphanet:319189", "chordo neural hinge": "UBERON:0007097", "cell envelope": "GO:0030313", "THS-seq": "EFO:0008969", "Hypogonadotropic hypogonadism - frontoparietal alopecia": "Orphanet:2230", "glial cell": "CL:0000125", "Spondylocamptodactyly syndrome": "Orphanet:3180", "1-methylhistidine {http": "CHEBI:70958", "GM17790 {http": "CLO:0016687", "pyoderma": "HP:0000999", "Sanjad-Sakati syndrome": "Orphanet:2323", "O-3-methylglutarylcarnitine {http": "CHEBI:70857", "nose morphology measurement": "EFO:0007843", "Enterococcus faecalis V583": "NCBITaxon:226185", "renal artery": "UBERON:0001184", "long day length regimen": "EO:0007199", "immature CD8_alpha-negative CD11b-positive dendritic cell": "CL:0000997", "insecticide": "CHEBI:24852", "Atrial septal defect - atrioventricular conduction defects": "Orphanet:1479", "Shwachman-Diamond syndrome": "Orphanet:811", "comparative genomic hybridization by array": "EFO:0000749", "Other genetic epidermal disease": "Orphanet:79360", "CS57560": "EFO:0000015", "C32TG": "EFO:0002119", "Renal pseudohypoaldosteronism type 1": "Orphanet:171871", "Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency": "Orphanet:83639", "vaccenic acid measurement": "EFO:0007974", "Muscular dystrophy": "Orphanet:98473", "GM14448 {http": "CLO:0031261", "CS57867": "EFO:0000149", "gulonic acid {http": "CHEBI:24462", "idiopathic osteonecrosis of the femoral head": "EFO:1001930", "plasma betaine measurement": "EFO:0007787", "Xylella fastidiosa 9a5c": "NCBITaxon:160492", "recombination": "EFO:0004293", "Mus musculus musculus": "NCBITaxon:39442", "tail": "UBERON:0002415", "osteoma": "EFO:0002423", "4p16.3 microduplication syndrome": "Orphanet:96072", "TRAP-Seq": "EFO:0008975", "NCI-H82": "EFO:0002306", "granulocytopoietic cell": "CL:0002191", "Pinus strobus": "NCBITaxon:3348", "Isolated congenital megalocornea": "Orphanet:91489", "MHC class I polypeptide-related sequence B measurement": "EFO:0008234", "increased risk": "EFO:0005847", "Neurothekeoma": "EFO:1000394", "alcohol dehydrogenase [NADP+] measurement": "EFO:0008017", "Craniosynostosis - intracranial calcifications": "Orphanet:52054", "indomethacin": "CHEBI:49662", "vasculature": "UBERON:0002049", "Chordoma": "Orphanet:178", "Ehlers-Danlos syndrome type 1": "Orphanet:90309", "progressive bulbar palsy": "EFO:0003783", "susceptibility to shingles measurement": "EFO:0008401", "Phlebitis": "EFO:1001395", "Rare genetic female infertility": "Orphanet:400008", "Cervus elaphus hispanicus": "NCBITaxon:141655", "Hartsfield-Bixler-Demyer syndrome": "Orphanet:2117", "CS57521": "EFO:0000006", "Genetic susceptibility to infections due to particular pathogens": "Orphanet:183710", "CD34-positive, CD41-positive, CD42-positive megakaryocyte progenitor cell": "CL:0002023", "cardiomyopathy": "EFO:0000318", "Mandibular hypoplasia-deafness-progeroid syndrome": "Orphanet:363649", "eccrine sweat gland": "UBERON:0000423", "cobalamin metabolic process": "GO:0009235", "TCR-alpha-beta-positive T-cell deficiency": "Orphanet:397959", "Arabis mosaic virus": "NCBITaxon:12271", "Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome": "Orphanet:363611", "GM17782 {http": "CLO:0016642", "dermatitis herpetiformis": "EFO:1000684", "Galactose epimerase deficiency": "Orphanet:79238", "epithelioid and spindle cell nevus": "EFO:1000925", "Otomandibular dysplasia associated with monogenic syndromes": "Orphanet:156202", "Autosomal recessive progressive external ophthalmoplegia": "Orphanet:254886", "musculature of body": "UBERON:0000383", "myometrium": "UBERON:0001296", "Bluetongue virus 2": "NCBITaxon:35328", "Focal palmoplantar and gingival keratoderma": "Orphanet:2200", "methimazole": "CHEBI:50673", "spondyloarthropathy": "EFO:0000706", "embryonic esophageal ganglion": "FBbt:00005670", "trunk neural crest": "UBERON:0003083", "Familial thyroid dyshormonogenesis": "Orphanet:95716", "palatoquadrate arch": "UBERON:0011085", "Waardenburg syndrome type 3": "Orphanet:896", "CD14-positive, CD16-positive monocyte": "CL:0002397", "MHC-II-high non-classical monocyte": "CL:0002473", "CLAPO syndrome": "Orphanet:168984", "Micro syndrome": "Orphanet:2510", "Oculotrichodysplasia": "Orphanet:2718", "White sponge nevus": "Orphanet:171723", "digestive system": "UBERON:0001007", "Congenital pseudoarthrosis of the ulna": "Orphanet:295026", "corpus striatum": "UBERON:0000369", "Lymphomatoid Papulosis": "EFO:1000341", "Metazoa {http": "NCBITaxon:33208", "paracetamol": "CHEBI:46195", "Early-onset generalized limb-onset dystonia": "Orphanet:256", "leaf lamina": "PO:0020039", "Acheiropodia": "Orphanet:931", "ciliary ganglion": "UBERON:0002058", "MS589": "EFO:0002838", "nucleic acid hybridization": "OBI:0302903", "Oral leukoplakia": "HP:0002745", "Angioosteohypotrophic syndrome": "Orphanet:75508", "activated CD4-negative, CD8-negative type I NK T cell": "CL:0000928", "Medullary Cystic Kidney Disease Type I": "EFO:0008617", "Epidermolysis bullosa simplex with pyloric atresia": "Orphanet:158684", "Monteggia's fracture": "EFO:1001811", "beta amyloid": "CHEBI:64645", "Glycogen storage disease due to muscle beta-enolase deficiency": "Orphanet:99849", "NARP syndrome": "Orphanet:644", "Congenital tracheomalacia": "Orphanet:95430", "serotonin": "CHEBI:28790", "Genetic polyendocrinopathy": "Orphanet:183643", "presumptive rhombomere 7": "UBERON:0007294", "Hypomyelination with atrophy of basal ganglia and cerebellum": "Orphanet:139441", "mass": "PATO:0000125", "phototoxic dermatitis": "EFO:1000753", "halothane": "CHEBI:5615", "Hypertrichosis": "Orphanet:79365", "Tall stature {http": "HP:0000098", "Arachnodactyly - abnormal ossification - intellectual disability": "Orphanet:1129", "Cutis laxa": "Orphanet:209", "GM17803 {http": "CLO:0016496", "Genito-palato-cardiac syndrome": "Orphanet:2075", "Peters anomaly - cataract": "Orphanet:101033", "Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy": "Orphanet:217591", "tiglylglycine {http": "CHEBI:73018", "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia": "Orphanet:317476", "Thick lower lip vermilion {http": "HP:0000179", "Fatal infantile cytochrome C oxidase deficiency": "Orphanet:1561", "canrenoate": "CHEBI:50159", "necrotizing sialometaplasia": "EFO:1001057", "Humero-radio-ulnar synostosis, bilateral": "Orphanet:295207", "Fingerprint body myopathy": "Orphanet:97232", "Sebastes melanops": "NCBITaxon:72085", "very low density lipoprotein particle size measurement": "EFO:0008594", "hepatocyte growth factor-like protein measurement": "EFO:0008154", "cerebrovascular endothelial cell": "BTO:0000238", "stem Cell Growth Factor beta measurement": "EFO:0008292", "Otofaciocervical syndrome": "Orphanet:2792", "Pseudomonas fluorescens Pf0-1": "NCBITaxon:205922", "dorsal telencephalon": "UBERON:0000203", "giant cell reparative granuloma": "EFO:1000950", "gastroesophageal reflux disease": "EFO:0003948", "sarcocystosis": "EFO:0007476", "Genetic hyperparathyroidism": "Orphanet:208596", "succinate(2-) {http": "CHEBI:30031", "IBL4": "EFO:0002060", "X-linked hereditary sensory and autonomic neuropathy with deafness": "Orphanet:139583", "Tachycardia, Reciprocating": "EFO:1001432", "ascitic fluid": "UBERON:0007795", "interleukin 25 measurement": "EFO:0008182", "metastasis measurement": "EFO:0007675", "red wine liking measurement": "EFO:0006947", "Lactobacillus reuteri": "NCBITaxon:1598", "1-palmitoyl-2-linoleoyl-sn-glycerol {http": "CHEBI:82927", "Thermotoga neapolitana": "NCBITaxon:2337", "B6C3F1": "EFO:0001340", "Pyloric Gland Adenoma": "EFO:1000501", "sphinganine {http": "CHEBI:16566", "postpartum depression": "EFO:0007453", "Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency": "Orphanet:363543", "protocol parameter": "EFO:0002658", "Abnormality of bronchi": "HP:0002109", "Olfactory Neuroblastoma": "EFO:1000407", "consultant": "EFO:0001732", "Rift Valley fever virus": "NCBITaxon:11588", "glycoprotein biosynthetic process": "GO:0009101", "electrocardiography": "EFO:0004327", "systolic blood pressure change measurement": "EFO:0006944", "Genetic non-syndromic obesity": "Orphanet:98267", "reactive arthritis": "EFO:0007460", "cytoskeleton": "GO:0005856", "embryonic stage 10": "EFO:0005870", "Acro-oto-ocular syndrome": "Orphanet:2980", "calf circumference measurement": "EFO:0008453", "Symplocarpus renifolius": "NCBITaxon:477955", "CCL11 measurement": "EFO:0005188", "Hypoplasminogenemia": "Orphanet:722", "head and neck neoplasia": "EFO:0005950", "embryonic day 8.25": "EFO:0002561", "10-trans,12-cis-octadecadienoic acid": "CHEBI:44526", "Lesch-Nyhan syndrome": "Orphanet:510", "Erythromelalgia": "Orphanet:1956", "rhombomere 5 floor plate": "UBERON:0005579", "RERF-GC-1B": "EFO:0006743", "HepG2": "EFO:0001187", "Patch-seq": "EFO:0008853", "posterior lateral line primordium": "UBERON:2001157", "GM17250 {http": "CLO:0014397", "Partial duplication of the long arm of chromosome X": "Orphanet:263783", "Illumina MiniSeq": "EFO:0008636", "Sphingolipidosis": "Orphanet:79225", "Oligosaccharidosis": "Orphanet:79215", "GM14414 {http": "CLO:0031225", "steroid": "CHEBI:35341", "femtomole per nanogram": "EFO:0005314", "1-methylxanthine {http": "CHEBI:68443", "plasmodium parasite stage": "EFO:0002544", "McKusick-Kaufman syndrome": "Orphanet:2473", "Deinococcus": "NCBITaxon:1298", "struma ovarii": "EFO:1001192", "derived time unit": "UO:0000149", "Infantile spasms - broad thumbs": "Orphanet:3173", "Desmin-related myopathy with Mallory body-like inclusions": "Orphanet:84132", "Mosaic trisomy 8": "Orphanet:96061", "mononuclear cell": "CL:0000842", "response to candesartan": "GO:1901556", "exploratory behavior": "EFO:0004316", "COM-3 cell": "BTO:0004263", "IMR-32": "EFO:0001195", "Ventricular septal defect": "Orphanet:1480", "ventral nerve cord": "UBERON:0000934", "Naxos disease": "Orphanet:34217", "Xenograft": "EFO:0003942", "Pineocytoma": "EFO:1000476", "candela": "UO:0000014", "superior crus of antihelix expression": "EFO:0007673", "IgE plasma cell": "CL:0000947", "SK-N-DZ": "EFO:0005721", "N syndrome": "Orphanet:2608", "single cell specimen": "EFO:0007831", "Transient hypogammaglobulinemia of infancy": "Orphanet:169139", "Congenital muscular dystrophy due to LMNA mutation": "Orphanet:157973", "Schizosaccharomyces japonicus": "NCBITaxon:4897", "Partial chromosome Y deletion": "Orphanet:1646", "interferon alpha": "EFO:0003021", "Stimmler syndrome": "Orphanet:3199", "patellofemoral pain syndrome": "EFO:1001092", "seropositivity measurement": "EFO:0007034", "tissue culture": "BTO:0001384", "Hypertrichosis cubiti - short stature": "Orphanet:2220", "pantothenate metabolic process": "GO:0015939", "Autosomal recessive limb-girdle muscular dystrophy type 2B": "Orphanet:268", "Herpes simplex virus keratitis": "EFO:0007308", "Solanum tuberosum": "NCBITaxon:4113", "SK-N-MC": "EFO:0002860", "gastrointestinal tuberculosis": "EFO:0007280", "response to anticoagulant": "GO:0061476", "Hereditary sensory and autonomic neuropathy type 1B": "Orphanet:139564", "Gollop-Wolfgang complex": "Orphanet:1986", "tibial nerve": "UBERON:0001323", "Curry-Jones syndrome": "Orphanet:1553", "GM17281 {http": "CLO:0013097", "Leukonychia totalis - acanthosis-nigricans-like lesions - abnormal hair": "Orphanet:210133", "Choanal atresia-deafness-cardiac defects-dysmorphism syndrome": "Orphanet:1200", "Wolfram syndrome": "Orphanet:3463", "RAW264.7": "EFO:0001231", "Benign paroxysmal torticollis of infancy": "Orphanet:71518", "CD141-positive myeloid dendritic cell": "CL:0002394", "primary cell line": "EFO:0003064", "RDES": "EFO:0002316", "Syndactyly - telecanthus - anogenital and renal malformations": "Orphanet:140952", "ribonate {http": "CHEBI:33527", "cP-RNA-Seq": "EFO:0008697", "krebs 2 carcinoma": "EFO:1001007", "Mimulus guttatus": "NCBITaxon:4155", "Major Salivary Gland Mucoepidermoid Carcinoma": "EFO:1000346", "NCI-H522": "EFO:0002295", "Congenital alveolar capillary dysplasia": "Orphanet:210122", "Entamoeba invadens": "NCBITaxon:33085", "Osteonecrosis of genetic origin": "Orphanet:399380", "erythritol {http": "CHEBI:17113", "paroxetine maleate": "CHEBI:64194", "ICF syndrome": "Orphanet:2268", "ventricular system": "UBERON:0005281", "Angel-shaped phalango-epiphyseal dysplasia": "Orphanet:63442", "Bombyx mori": "NCBITaxon:7091", "nerve {http": "UBERON:0001021", "vitamin B6 measurement": "EFO:0004621", "Porencephaly": "Orphanet:2940", "composite lymphoma": "EFO:0007215", "embryo sac {http": "PO:0025074", "Autosomal dominant limb-girdle muscular dystrophy type 1F": "Orphanet:55595", "MX distant metastasis stage": "EFO:0004931", "Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency": "Orphanet:71212", "hormone measurement": "EFO:0004730", "Tae-Eum": "EFO:0007122", "Charcot-Marie-Tooth disease type 4C": "Orphanet:99949", "Conductive deafness - ptosis - skeletal anomalies": "Orphanet:3236", "protein kinase inhibitor": "CHEBI:37699", "adenine {http": "CHEBI:16708", "basal endosperm transfer layer {http": "PO:0025196", "acetoacetate": "CHEBI:13705", "chlorhexidine": "CHEBI:3614", "osteomalacia": "EFO:1002027", "Bacteroides fragilis": "NCBITaxon:817", "CB205": "EFO:0004077", "Unilateral renal dysplasia": "Orphanet:93172", "Vitreoretinal degeneration": "Orphanet:98670", "129xC57BL/6": "EFO:0000601", "Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome": "Orphanet:397927", "Partial deletion of the short arm of chromosome 8": "Orphanet:261920", "sporophyte meristematic apical cell {http": "PO:0030015", "Isolated lissencephaly type 1 without known genetic defects": "Orphanet:1084", "Infantile epileptic-dyskinetic encephalopathy": "Orphanet:364063", "interstitial lung disease": "EFO:0004244", "Bradyrhizobium japonicum USDA 110": "NCBITaxon:224911", "Hirschsprung disease - nail hypoplasia - dysmorphism": "Orphanet:2153", "volume": "EFO:0001715", "Pelvis-shoulder dysplasia": "Orphanet:2839", "putamen volume": "EFO:0006932", "mannose measurement": "EFO:0006958", "embryonic labial sensory complex": "FBbt:00005619", "Rare hereditary metabolic disease with peripheral neuropathy": "Orphanet:207018", "GMUCT 2.0": "EFO:0008753", "susceptibility to cold sores measurement": "EFO:0008402", "language measurement": "EFO:0007797", "selenium": "CHEBI:27568", "very low birth weight infant": "EFO:0003965", "Werner syndrome": "Orphanet:902", "Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome": "Orphanet:369861", "colon": "UBERON:0001155", "Primary qualitative or quantitative defects of alpha-dystroglycan": "Orphanet:371040", "COLO 849": "EFO:0006379", "gamma-linolenic acid {http": "CHEBI:28661", "scRRBS": "EFO:0008914", "Autosomal dominant Charcot-Marie-Tooth disease type 2L": "Orphanet:99945", "left ventricular diastolic function measurement": "EFO:0008204", "pityriasis versicolor": "EFO:0007439", "Aphonia - deafness - retinal dystrophy - bifid halluces - intellectual disability": "Orphanet:324540", "chronic": "HP:0011010", "investigation": "OBI:0000066", "petaloid toenail": "EFO:0007879", "agreeableness measurement": "EFO:0007915", "L-arginine measurement": "EFO:0006524", "Humero-radial synostosis, unilateral": "Orphanet:295209", "Endomyocardial fibroelastosis": "Orphanet:2022", "Isolated oxidative phosphorylation complex disorder": "Orphanet:254846", "Growth retardation-mild developmental delay-chronic hepatitis syndrome": "Orphanet:391366", "Hirschmanniella oryzae {http": "NCBITaxon:362338", "malignant hyperthermia, susceptibility to, 1": "EFO:0009071", "Rhinitis, Allergic, Perennial": "EFO:1001417", "Autosomal recessive cutis laxa type 2, classic type": "Orphanet:357074", "granulocyte colony-stimulating factor measurement": "EFO:0008142", "cotyledon abaxial epidermis": "PO:0006057", "G130": "EFO:0006402", "dioxygen(2+)": "CHEBI:29371", "Pleural Mesothelioma": "EFO:1000485", "Congenital absence of both forearm and hand, bilateral": "Orphanet:295095", "pluripotent": "EFO:0002967", "imipramine": "CHEBI:47499", "N(5)-ethyl-L-glutamine {http": "CHEBI:17394", "Streptococcus thermophilus CNRZ1066": "NCBITaxon:299768", "pro-B cell": "CL:0000826", "Torg-Winchester syndrome": "Orphanet:3460", "double-positive, alpha-beta thymocyte": "CL:0000809", "Syndromic retinitis pigmentosa": "Orphanet:98661", "thyroid crisis": "EFO:1001212", "Fountain syndrome": "Orphanet:3219", "phosgene": "CHEBI:29365", "Intellectual disability-seizures-macrocephaly-obesity syndrome": "Orphanet:369950", "Colon Sessile Serrated Adenoma/Polyp": "EFO:1000189", "Familial bicuspid aortic valve": "Orphanet:402075", "thoracic outlet syndrome": "EFO:0007507", "R wave amplitude": "EFO:0007741", "Intraocular melanoma {http": "HP:0007716", "Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency": "Orphanet:352563", "male accessory sex gland {http": "UBERON:0010147", "Maternal uniparental disomy of chromosome 1": "Orphanet:251009", "GM1 gangliosidosis type 2": "Orphanet:79256", "Split hand, bilateral": "Orphanet:295122", "bone density": "EFO:0003923", "breast neoplasm": "EFO:0003869", "Benign Skin Appendage Neoplasm": "EFO:1000120", "Isochromosome Y": "Orphanet:96325", "Autosomal recessive intermediate Charcot-Marie-Tooth disease type C": "Orphanet:369867", "1q41q42 microdeletion syndrome": "Orphanet:250999", "fibroepithelial polyp of the anus": "EFO:1000699", "Greenberg dysplasia": "Orphanet:1426", "ovarian disease": "EFO:0005771", "Rare hemorrhagic disorder due to a constitutional platelet anomaly": "Orphanet:71202", "Ketoacidosis due to beta-ketothiolase deficiency": "Orphanet:134", "Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome": "Orphanet:391487", "leaf {http": "PO:0025034", "Buchnera aphidicola (Schizaphis graminum)": "NCBITaxon:98794", "PMA": "EFO:0008864", "carcinoma": "EFO:0000313", "Schizosaccharomyces pombe 972h-": "NCBITaxon:284812", "Primary failure of tooth eruption": "Orphanet:412206", "Benign childhood occipital epilepsy, Gastaut type": "Orphanet:98816", "Hereditary cerebral hemorrhage with amyloidosis, Flemish type": "Orphanet:324718", "Arnold-Chiari malformation type II": "Orphanet:1136", "plant developmental tissue": "EFO:0000999", "secreted protein identification design": "EFO:0001786", "Zollinger-Ellison Syndrome": "EFO:0007549", "pulmonary embolism": "EFO:0003827", "Cranial nerve and nuclear aplasia": "Orphanet:98518", "mouse cell line": "EFO:0002887", "double-positive blast": "CL:0002428", "theta wave measurement": "EFO:0006873", "immature interstitial dendritic cell": "CL:0001011", "Invasive Breast Carcinoma": "EFO:1000307", "larval stage": "UBERON:0000069", "methionine sulfone {http": "CHEBI:21363", "mesencephalic neural crest": "UBERON:0003849", "HEK293": "EFO:0001182", "dimercaprol": "CHEBI:64198", "European bat lyssavirus 1": "NCBITaxon:57482", "9p13 microdeletion syndrome": "Orphanet:324313", "mental health": "EFO:0003935", "subependymal glioma": "EFO:1001197", "Nabothian Cyst": "EFO:1000390", "White matter hypoplasia - corpus callosum agenesis - intellectual disability": "Orphanet:3207", "primary metabolic process": "GO:0044238", "Ovarian Sertoli-Leydig Cell Tumor": "EFO:1000429", "Harpagifer antarcticus": "NCBITaxon:43256", "respiratory symptom measurement": "EFO:0007939", "nicotine": "CHEBI:18723", "Endometrial Endometrioid Adenocarcinoma": "EFO:1000233", "GM10843 {http": "CLO:0023785", "2-methylcitrate (3-) {http": "CHEBI:15598", "Hi-0": "EFO:0006980", "osteoarthritis, spine": "EFO:1000787", "docosapentaenoic acid": "CHEBI:61204", "postoperative ventricular dysfunction": "EFO:0004889", "Disorder of purine metabolism": "Orphanet:79191", "Yoruba": "EFO:0004900", "chromosomal aberration": "EFO:0000336", "Autosomal dominant prognathism": "Orphanet:2964", "complete blood cell count": "EFO:0004586", "Immunodeficiency syndrome with hypopigmentation": "Orphanet:331249", "Mus": "NCBITaxon:10088", "Staphylococcus aureus subsp. aureus str. Newman": "NCBITaxon:426430", "Disorder of galactose metabolism": "Orphanet:308467", "Candidiasis, Invasive": "EFO:1001283", "Autosomal recessive distal hereditary motor neuropathy": "Orphanet:140468", "diabetic ketoacidosis": "EFO:1000897", "organochlorine pesticides": "CHEBI:25705", "Retinal degeneration - nanophthalmos - glaucoma": "Orphanet:1574", "Nossen ecotype": "EFO:0006975", "Whipple's disease": "EFO:0000775", "Bromus secalinus": "NCBITaxon:4502", "CS57570": "EFO:0000018", "Danio rerio larval stage": "EFO:0007695", "simple cystadenoma": "EFO:0002511", "Myasthenic syndrome with eye involvement": "Orphanet:98690", "Qualitative or quantitative defects of filamin C": "Orphanet:209047", "GM17766 {http": "CLO:0016594", "malate(2-) {http": "CHEBI:15595", "X-linked sideroblastic anemia": "Orphanet:75563", "embryonic proventriculus outer layer": "FBbt:00005610", "anaplastic oligoastrocytoma": "EFO:0002500", "Mus caroli": "NCBITaxon:10089", "Pelvic dysplasia - arthrogryposis of lower limbs": "Orphanet:2840", "stage I endometrioid carcinoma": "EFO:0000205", "GM11839": "EFO:0001121", "nutritional disorder": "EFO:0001069", "Dysequilibrium syndrome": "Orphanet:1766", "Hyperplastic polyposis syndrome": "Orphanet:157798", "somite 3": "UBERON:2000732", "TELO2-related intellectual disability-neurodevelopmental disorder": "EFO:0009061", "Panc89": "EFO:0002714", "gestational hematopoietic stem cell": "CL:0002352", "Kit-negative, Ly-76 high polychromatophilic erythroblast": "CL:0002015", "blood sedimentation": "EFO:0004304", "Loose anagen syndrome": "Orphanet:168", "Dedifferentiated Solitary Fibrous Tumor": "EFO:1000214", "Setaria italica": "NCBITaxon:4555", "CS57908": "EFO:0000164", "ependymal neoplasm": "EFO:1000027", "trunk mesoderm anlage": "UBERON:6005436", "Bleeding diathesis due to a collagen receptor defect": "Orphanet:73271", "papillary follicular thyroid adenocarcinoma": "EFO:1001083", "KATOIII": "EFO:0002217", "Autosomal dominant progressive external ophthalmoplegia": "Orphanet:254892", "Muscular hypertrophy - hepatomegaly - polyhydramnios": "Orphanet:324416", "tuberculin skin test reactivity measurement": "EFO:0008307", "lipid or lipoprotein measurement": "EFO:0005105", "allergenic agent": "CHEBI:50904", "failure to thrive {http": "HP:0001508", "case control design": "EFO:0001427", "immature gamma-delta T cell": "CL:0000799", "CS57727": "EFO:0000076", "Temtamy preaxial brachydactyly syndrome": "Orphanet:363417", "GM17794 {http": "CLO:0016676", "Osteochondroma": "EFO:1000411", "gamma-Glu-Ile {http": "CHEBI:68434", "e-selectin measurement": "EFO:0004575", "2-methyl-6-(phenylethynyl)pyridine hydrochloride": "CHEBI:64158", "Thymic aplasia": "Orphanet:83471", "Prelingual non-syndromic genetic deafness": "Orphanet:216445", "Moyamoya disease": "Orphanet:2573", "Buruli Ulcer": "EFO:1001281", "Cornelia de Lange syndrome": "Orphanet:199", "epithelium of bronchus": "UBERON:0002031", "Persea americana": "NCBITaxon:3435", "Neisseriaceae Infections": "EFO:1001377", "Distal trisomy 2p": "Orphanet:96070", "TANOUE": "EFO:0002380", "GTI-Seq": "EFO:0008759", "Drosophila melanogaster": "NCBITaxon:7227", "Autosomal dominant spastic paraplegia type 31": "Orphanet:101011", "Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria": "Orphanet:1933", "X-linked intellectual disability, Raynaud type": "Orphanet:3061", "Multiple epiphyseal dysplasia due to collagen 9 anomaly": "Orphanet:166002", "cathepsin B measurement": "EFO:0008072", "presumptive brain": "UBERON:0006238", "Upper thoracic spina bifida aperta": "Orphanet:268740", "brain disease": "EFO:0005774", "Autosomal recessive polycystic kidney disease": "Orphanet:731", "alcohol withdrawal": "EFO:0004777", "caffeine metabolite measurement": "EFO:0007872", "neural rod": "UBERON:0005068", "Digitotalar dysmorphism": "Orphanet:1146", "267B1 Ki-ras": "EFO:0001081", "3\u00e2\u0080\u00b2-Seq": "EFO:0008643", "red light regimen": "EO:0007207", "Nevus comedonicus syndrome": "Orphanet:64754", "X-linked intellectual disability, Gu type": "Orphanet:3059", "Glycine max": "NCBITaxon:3847", "Xeroderma pigmentosum complementation group A": "Orphanet:276249", "descending octaval nucleus": "UBERON:2000645", "Equisetum arvense {http": "NCBITaxon:3258", "GM14480 {http": "CLO:0031534", "brain edema": "EFO:1000845", "Charcot-Marie-Tooth disease - deafness - intellectual disability": "Orphanet:90103", "Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome": "Orphanet:306558", "lung epithelium": "UBERON:0000115", "Mammary-digital-nail syndrome": "Orphanet:238744", "GM17117 {http": "CLO:0014950", "Isolated delta-storage pool disease": "Orphanet:248340", "pre-natural killer cell": "CL:0000937", "polidocanol": "CHEBI:46859", "COV413B": "EFO:0006558", "pilar sheath acanthoma": "EFO:1001107", "Partial deletion of the long arm of chromosome 1": "Orphanet:262001", "Mucopolysaccharidosis type 4": "Orphanet:582", "Muscle weakness {http": "HP:0001324", "Small Intestinal Burkitt Lymphoma": "EFO:1000533", "Primary ciliary dyskinesia": "Orphanet:244", "purine nucleoside biosynthetic process": "GO:0042451", "Human herpesvirus 6B": "NCBITaxon:32604", "abnormal renal physiology": "HP:0012211", "Monosomy 9q22.3": "Orphanet:77301", "Malignant Germ Cell Tumor": "EFO:1000352", "cardiac arrhythmia": "EFO:0004269", "Thyroid Gland Mucoepidermoid Carcinoma": "EFO:1000590", "spondin-1 measurement": "EFO:0008290", "MHC class I polypeptide-related sequence A measurement": "EFO:0008233", "CADASIL": "Orphanet:136", "[Pyruvate dehydrogenase acetyl-transferring] kinase isozyme 1, mitochondrial measurement": "EFO:0008010", "ND04158 {http": "CLO:0032601", "Methylmalonic acidemia without homocystinuria": "Orphanet:293355", "pH regimen": "EO:0007171", "chronic hepatitis": "EFO:0008496", "Bordetella parapertussis": "NCBITaxon:519", "Progressive supranuclear palsy - corticobasal syndrome": "Orphanet:240103", "Patski {http": "EFO:0005481", "Noccaea caerulescens": "NCBITaxon:107243", "palmitoyl ethanolamide {http": "CHEBI:71464", "treatment-resistant hypertension": "EFO:1002006", "smMIP": "EFO:0008935", "Dense deposit disease": "Orphanet:93571", "ficolin-2 measurement": "EFO:0008135", "ONT GridION X5": "EFO:0008633", "Dyschromatosis symmetrica hereditaria": "Orphanet:41", "Ossifying Renal Tumor of Infancy": "EFO:1000409", "chronic lymphocytic leukemia": "EFO:0000095", "WM115": "EFO:0002390", "Benign Thyroid Gland Neoplasm": "EFO:1000122", "reverse transcription PCR": "OBI:0000552", "cutaneous nodular amyloidosis": "EFO:1001882", "Intellectual disability - short stature - hypertelorism": "Orphanet:3074", "Capillary malformation - arteriovenous malformation": "Orphanet:137667", "tomatine": "CHEBI:9630", "Unclassified familial retinal dystrophy": "Orphanet:98662", "Dnase I SIM": "EFO:0008715", "Hawaiian": "EFO:0003168", "CS57716": "EFO:0000072", "Toscana virus": "NCBITaxon:11590", "Pyruvate dehydrogenase phosphatase deficiency": "Orphanet:79246", "Cataract-congenital heart disease-neural tube defect syndrome": "Orphanet:314993", "GM08436 {http": "CLO:0010557", "EAST syndrome": "Orphanet:199343", "B220-low CD38-negative unswitched memory B cell": "CL:0002113", "Monosomy 13q14": "Orphanet:1587", "p-tau": "EFO:0007709", "ESC derived cell line": "EFO:0005738", "Streptomyces virginiae": "NCBITaxon:1961", "Ectocarpus": "NCBITaxon:2879", "Bulbar conjunctival dermoid or conjunctival dermolipoma": "Orphanet:98617", "anal fin": "UBERON:4000163", "Tarsal kink syndrome": "Orphanet:99170", "Urban-Rogers-Meyer syndrome": "Orphanet:3409", "platelet glycoprotein VI measurement": "EFO:0008263", "M1 distant metastasis stage": "EFO:0004930", "mouse postnatal": "EFO:0004390", "PEHO syndrome": "Orphanet:2836", "sulfasalazine": "CHEBI:9334", "HCC1500": "EFO:0001172", "resistin measurement": "EFO:0004819", "surfactant protein D measurement": "EFO:0005081", "YCC7": "EFO:0002882", "lymphoblast": "EFO:0000572", "estrogen receptor activity": "GO:0030284", "Trichophyton soudanense": "NCBITaxon:69891", "Lipoprotein glomerulopathy": "Orphanet:329481", "Acromicric dysplasia": "Orphanet:969", "Palpebral lentiginosis": "Orphanet:98587", "N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide": "CHEBI:63996", "phosphate": "CHEBI:26020", "Rare disease with glaucoma as a major feature": "Orphanet:98638", "immature eosinophil": "CL:0000772", "Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome": "Orphanet:313846", "oligomycin A": "CHEBI:28285", "Cataract - intellectual disability - hypogonadism": "Orphanet:1387", "Cyanophage S-BnM1": "NCBITaxon:65016", "Constitutional sideroblastic anemia": "Orphanet:98362", "X-linked intellectual disability, Seemanova type": "Orphanet:85323", "response to duloxetine": "EFO:0008345", "paragonimiasis": "EFO:0007418", "galactonate {http": "CHEBI:24148", "Pericardial and diaphragmatic defect": "Orphanet:2847", "initial pursuit acceleration": "EFO:0008434", "Drosophila pseudoobscura": "NCBITaxon:7237", "Congenital intestinal transport defect": "Orphanet:104003", "Halobacterium sp. NRC-1": "NCBITaxon:64091", "Renal-hepatic-pancreatic dysplasia": "Orphanet:294415", "anaplastic lung carcinoma": "EFO:1000016", "Triticum urartu": "NCBITaxon:4572", "tetanus": "EFO:0005593", "ILSXISS84/TejJ": "EFO:0002994", "Anopheles arabiensis": "NCBITaxon:7173", "hypoglycemic drug": "CHEBI:35526", "Aminoacylase 1 deficiency": "EFO:1001981", "Eczema": "HP:0000964", "flower development stage {http": "PO:0007615", "Ascites": "HP:0001541", "MCIXC": "EFO:0002230", "Fraction C' precursor B cell": "CL:0002050", "pharyngeal arch cartilage": "UBERON:0011004", "Autosomal recessive disease with focal palmoplantar keratoderma as a major feature": "Orphanet:98357", "response to flupirtine": "EFO:0007809", "spontaneous abortion {http": "EFO:1001255", "verapamil": "CHEBI:9948", "light regimen {http": "EO:0007196", "undifferentiated pleomorphic sarcoma": "EFO:1001972", "Hemolytic anemia due to erythrocyte adenosine deaminase overproduction": "Orphanet:99138", "nucleic acid sequencing protocol": "EFO:0004170", "Haematobia irritans": "NCBITaxon:7368", "Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency": "Orphanet:279934", "AG11696 {http": "CLO:0022362", "Autosomal recessive spastic ataxia": "Orphanet:316240", "Autosomal recessive limb-girdle muscular dystrophy type 2G": "Orphanet:34514", "necrobiosis lipoidica": "EFO:1000738", "OCI-LY7": "EFO:0006711", "Donnai-Barrow syndrome": "Orphanet:2143", "hepatitis E": "EFO:0007303", "mature dendritic epithelial T cell precursor": "CL:0002401", "posterior spiracle primordium": "FBbt:00000197", "GM15850": "EFO:0006276", "0 seed germination stage": "PO:0007057", "renal aminoaciduria": "EFO:1001149", "Combined oxidative phosphorylation defect type 25": "EFO:0009035", "Digenome-seq": "EFO:0008709", "anti-arrhythmia drug": "CHEBI:38070", "Enterovirus infectious disease": "EFO:0007255", "Beta-mannosidosis": "Orphanet:118", "acarbose": "CHEBI:2376", "Mesenchymatous palpebral tumor": "Orphanet:98591", "Cystathioninuria": "Orphanet:212", "Myotonia fluctuans": "Orphanet:99734", "myeloid sarcoma": "EFO:1001052", "Paramecium bursaria Chlorella virus 1": "NCBITaxon:10506", "postpartum": "EFO:0008562", "Galloway-Mowat syndrome": "Orphanet:2065", "Col-4": "EFO:0005152", "Val-Gly {http": "CHEBI:73699", "Benign familial neonatal-infantile seizures": "Orphanet:140927", "Nicotiana langsdorffii x Nicotiana sanderae": "NCBITaxon:164110", "Candida albicans WO-1": "NCBITaxon:294748", "Annular pancreas": "Orphanet:675", "CS57807": "EFO:0000123", "Distal myopathy, Welander type": "Orphanet:603", "X-linked congenital disorder of glycosylation with intellectual disability as a major feature": "Orphanet:371054", "Trichophyton schoenleinii": "NCBITaxon:34386", "Liriodendron tulipifera": "NCBITaxon:3415", "Severe intellectual disability-short stature-behavioral troubles-facial dysmorphism syndrome": "Orphanet:391307", "Say-Barber-Miller syndrome": "Orphanet:3132", "GM2": "EFO:0005747", "Pseudomonas putida KT2440": "NCBITaxon:160488", "HeLa": "EFO:0001185", "TUBO": "EFO:0006306", "Lymphatic Metastasis": "EFO:1001364", "pharyngeal pouch 6": "UBERON:0007127", "funder": "EFO:0001736", "hearing threshold measurement": "EFO:0007618", "chordate pharynx": "UBERON:0001042", "Colinus virginianus": "NCBITaxon:9014", "embryonic stage 12": "EFO:0005872", "anti-cyclic citrullinated peptide antibody measurement": "EFO:0004733", "Carassius auratus": "NCBITaxon:7957", "Coloboma of inferior eyelid": "Orphanet:155889", "GM00144 {http": "CLO:0025850", "total particulate matter per liter": "EFO:0004386", "46,XY disorder of sex development due to isolated 17,20 lyase deficiency": "Orphanet:90796", "concentration of": "PATO:0000033", "CS57598": "EFO:0000028", "GM17244 {http": "CLO:0014414", "rotator cuff tear": "EFO:1001250", "ribitol {http": "CHEBI:15963", "executive function": "EFO:0007046", "aortic valve": "UBERON:0002137", "stem {http": "PO:0009047", "Atypical Rett syndrome": "Orphanet:3095", "Postpericardiotomy Syndrome": "EFO:1001404", "Brachydactyly": "Orphanet:294937", "MeWo": "EFO:0006648", "CI-1": "EFO:0006367", "yang deficiency": "EFO:0006817", "metabolomic profiling": "EFO:0000752", "Hereditary myoclonus - progressive distal muscular atrophy": "Orphanet:2590", "short day length regimen": "EO:0007200", "adipose macrophage": "CL:0002477", "Phaseolus coccineus": "NCBITaxon:3886", "Melampsora larici-populina": "NCBITaxon:203908", "Schizophyllum commune": "NCBITaxon:5334", "Cyanobacteria": "NCBITaxon:1117", "chitotriosidase-1 measurement": "EFO:0008084", "PEComa": "EFO:1000464", "Microcephaly-capillary malformation syndrome": "Orphanet:294016", "macula utricle": "UBERON:0002214", "Congenital muscular dystrophy": "Orphanet:97242", "Centripetalis recessive dystrophic epidermolysis bullosa": "Orphanet:89841", "Dent disease": "Orphanet:1652", "Kit-positive macrophage dendritic cell progenitor": "CL:0002011", "heptanoate {http": "CHEBI:32362", "female genital tuberculosis": "EFO:1000935", "Ectodermal dysplasia, trichoodontoonychial type": "Orphanet:1818", "Genetic branchial arch or oral-acral syndrome": "Orphanet:183576", "Hep3B": "EFO:0002205", "Anopheles gambiae S": "NCBITaxon:377270", "Intellectual disability-strabismus syndrome": "Orphanet:363528", "benign fibrous mesothelioma": "EFO:1000835", "delta-6 desaturase measurement": "EFO:0007765", "Von Willebrand disease type 2B": "Orphanet:166087", "Lysinuric protein intolerance": "Orphanet:470", "1-oleoyl-2-linoleoyl-sn-glycero-3-phosphocholine {http": "CHEBI:74670", "obstructive sleep apnea": "EFO:0003918", "carotid artery": "UBERON:0005396", "Bm4 B cell": "CL:0000966", "midline primordium": "FBbt:00005528", "NCI-H847": "EFO:0006696", "Frontootopalatodigital syndrome": "Orphanet:364541", "Infantile systemic hyalinosis": "Orphanet:2176", "Caldicellulosiruptor owensensis": "NCBITaxon:55205", "multiple myeloma": "EFO:0001378", "Abnormality of connective tissue": "HP:0003549", "Episodic ataxia type 5": "Orphanet:211067", "glutamate residue {http": "CHEBI:32484", "Newcastle disease": "EFO:0007395", "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency": "Orphanet:319539", "GM17845 {http": "CLO:0016453", "Atypical Werner syndrome": "Orphanet:79474", "HCjE": "EFO:0003139", "Enterococcus casseliflavus": "NCBITaxon:37734", "Dysostosis with limb and face anomalies as a major feature": "Orphanet:364571", "imatinib methanesulfonate": "CHEBI:31690", "Best vitelliform macular dystrophy": "Orphanet:1243", "Partial duplication of chromosome 17": "Orphanet:262677", "Decreased body weight {http": "HP:0004325", "GM15036 {http": "CLO:0030311", "Homocarnosinosis": "Orphanet:2168", "Agrobacterium tumefaciens": "NCBITaxon:358", "cathepsin Z measurement": "EFO:0008074", "OPM-2": "EFO:0006716", "EFO-27": "EFO:0006571", "date of birth": "EFO:0004950", "Isolated focal cortical dysplasia type I": "Orphanet:268961", "presumptive mesoderm": "UBERON:0006603", "Spastic paraparesis - deafness": "Orphanet:2815", "thioridazine": "CHEBI:9566", "circulating cell": "CL:0000080", "peripheral blood stem cell": "CL:0002246", "GM14584 {http": "CLO:0031668", "Revesz syndrome": "Orphanet:3088", "ILSXISS3/TejJ": "EFO:0002972", "absorbed dose unit": "UO:0000129", "Follicular atrophoderma-basal cell carcinoma": "Orphanet:79459", "sialic acid-binding Ig-like lectin 9 measurement": "EFO:0008286", "Humero-radio-ulnar synostosis, unilateral": "Orphanet:295205", "16-hydroxypalmitate {http": "CHEBI:55329", "Ewing sarcoma": "EFO:0000174", "Mopeia virus": "NCBITaxon:11629", "insertion": "EFO:0004016", "Gyps fulvus": "NCBITaxon:36247", "Cooper-Jabs syndrome": "Orphanet:1488", "Thyroid Gland Squamous Cell Carcinoma": "EFO:1000594", "GM17180 {http": "CLO:0013751", "pneumocystosis": "EFO:0007448", "GM17261 {http": "CLO:0013183", "Dicentrarchus labrax": "NCBITaxon:13489", "papillary thyroid carcinoma": "EFO:0000641", "Ect1": "EFO:0005264", "Ralstonia phage RSL1": "NCBITaxon:482058", "polysorbate 60": "CHEBI:53425", "anterior lateral line nerve": "UBERON:2000425", "DEOC-1": "EFO:0006563", "ascariasis": "EFO:0007154", "intradermal nevus": "EFO:1000995", "Laing early-onset distal myopathy": "Orphanet:59135", "antitragus size": "EFO:0007669", "tonsil cancer": "EFO:1001214", "GM15236 {http": "CLO:0027467", "pancreatic adenosquamous carcinoma": "EFO:0006732", "MCF12A": "EFO:0001202", "Hermansky-Pudlak syndrome without pulmonary fibrosis": "Orphanet:231512", "type III hypersensitivity reaction disease": "EFO:1001222", "Spina bifida - hypospadias": "Orphanet:3176", "lens placode": "UBERON:0003073", "dexamethasone": "CHEBI:41879", "Xeroderma pigmentosum-Cockayne syndrome complex": "Orphanet:220295", "common myeloid progenitor": "CL:0000049", "Benign infantile focal epilepsy with midline spikes and wave during sleep": "Orphanet:166308", "response to anthracycline-based chemotherapy": "EFO:0005257", "Overgrowth syndrome": "Orphanet:93460", "Sickle cell - hemoglobin C disease": "Orphanet:251365", "metapterygoid": "UBERON:2000240", "COLO668": "EFO:0002138", "Daudi": "EFO:0002169", "congenital syphilis": "EFO:0007219", "Atypical hemolytic-uremic syndrome with DGKE deficiency": "Orphanet:357008", "chloracne": "EFO:1001777", "Intellectual disability-facial dysmorphism-hand anomalies syndrome": "Orphanet:370010", "contagious pustular dermatitis": "EFO:0007222", "X-linked neurodegenerative syndrome, Bertini type": "Orphanet:85334", "Fenneropenaeus merguiensis": "NCBITaxon:71412", "RI-1": "EFO:0006477", "Genetic parenchymatous liver disease": "Orphanet:156604", "abnormality of the nervous system": "HP:0000707", "copper": "CHEBI:28694", "Pantoea agglomerans": "NCBITaxon:549", "Nanogrid RNA-Seq": "EFO:0008825", "RERF-LC-AI": "EFO:0002850", "Alien Hand Syndrome": "EFO:1001261", "DNA assay": "EFO:0001456", "TPE interval measurement": "EFO:0004644", "beta wave measurement": "EFO:0006871", "Pellagra-like skin rash - neurological manifestations": "Orphanet:2837", "high content analysis of cells by morphological and physical properties": "EFO:0005399", "estrogen receptor status": "EFO:0005512", "cercarium": "EFO:0007712", "lung": "UBERON:0002048", "adult hindgut precursor": "FBbt:00005646", "Ebola hemorrhagic fever": "EFO:0007243", "pulmonary amyloidosis": "EFO:1001910", "Benign Carotid Body Paraganglioma": "EFO:1000108", "type II hypersensitivity": "GO:0002445", "Advanved Chia-PET": "EFO:0008650", "Recessive X-linked ichthyosis": "Orphanet:461", "GM13649 {http": "CLO:0032713", "date of diagnosis": "EFO:0004953", "immature basophil": "CL:0000768", "Collimonas": "NCBITaxon:202907", "SS3-Seq": "EFO:0008948", "Cerulean cataract": "Orphanet:98989", "orotidine {http": "CHEBI:25722", "root meristem": "PO:0006085", "tanespimycin": "CHEBI:64153", "abamectin": "CHEBI:39214", "developing seed stage {http": "PO:0004506", "Alagille syndrome due to a JAG1 point mutation": "Orphanet:261619", "Familial thrombomodulin anomalies": "Orphanet:3324", "propofol": "CHEBI:44915", "BA/F3 cell": "BTO:0001516", "gene knock out": "EFO:0000506", "Micropterus salmoides": "NCBITaxon:27706", "Cervical Endometrioid Adenocarcinoma": "EFO:1000164", "reproductive system cell": "EFO:0002955", "cystic fibrosis associated meconium ileum": "EFO:0004608", "Fibular hemimelia, bilateral": "Orphanet:295083", "CINCA syndrome with NLRP3 mutations": "Orphanet:93365", "streptococcal pneumonia": "EFO:0007499", "Keratosis palmaris et plantaris - clinodactyly": "Orphanet:86919", "intracranial vasospasm": "EFO:1000994", "C-Cell Hyperplasia": "EFO:1000147", "saliva": "UBERON:0001836", "Genetic immune deficiency with skin involvement": "Orphanet:183494", "carotid artery geometry measurement": "EFO:0007717", "Hypomyelination neuropathy - arthrogryposis": "Orphanet:2680", "hexadecanedioate(2-) {http": "CHEBI:76276", "arylesterase enzyme measurement": "EFO:0005126", "Synechococcus phage S-RSM2": "NCBITaxon:264653", "cortisol measurement": "EFO:0005843", "Congenital disorder of glycosylation with deafness as a major feature": "Orphanet:371212", "linolenic acid": "CHEBI:25048", "ChIP-Chip": "EFO:0000748", "129 mouse strain": "EFO:0000597", "Hereditary thrombocytopenia with normal platelets": "Orphanet:268322", "Bovine mastitis": "EFO:1001765", "Streptococcus dysgalactiae subsp. equisimilis": "NCBITaxon:119602", "Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy": "Orphanet:255235", "HM7": "EFO:0006787", "abnormality of the urinary system physiology": "HP:0011277", "monocyte": "EFO:0007956", "Neuroferritinopathy": "Orphanet:157846", "femoral hernia": "EFO:1001791", "genetic trait": "EFO:0000511", "S462": "EFO:0006292", "integumental cell": "EFO:0000700", "loop design": "EFO:0001770", "salicylic acid": "CHEBI:16914", "Pol II CLIP": "EFO:0008865", "mevalonate": "CHEBI:25350", "4C": "EFO:0007690", "mixed cell type cancer": "EFO:0007373", "Progressive familial intrahepatic cholestasis type 2": "Orphanet:79304", "response to diisocyanate": "EFO:0006995", "Pycnodysostosis": "Orphanet:763", "Rare constitutional medullar aplasia": "Orphanet:68383", "pancreatectomy": "EFO:0002581", "Syngnathia multiple anomalies": "Orphanet:3262", "complex partial epilepsy": "EFO:1000877", "Mitochondrial myopathy with reversible cytochrome C oxidase deficiency": "Orphanet:254864", "ddRADseq": "EFO:0008707", "GM09585 {http": "CLO:0011391", "response to opioid": "EFO:0008541", "uterine corpus cancer": "EFO:0007532", "Acheiria, bilateral": "Orphanet:295103", "age-related cataract": "HP:0011141", "GDNF family receptor alpha-2 measurement": "EFO:0008138", "Heart-hand syndrome": "Orphanet:228184", "Apis mellifera": "NCBITaxon:7460", "pharyngula prim-15": "EFO:0001312", "NCI-H441": "EFO:0002292", "G401": "EFO:0002179", "motility assay": "EFO:0002908", "camptothecin": "CHEBI:27656", "Yersinia pseudotuberculosis": "NCBITaxon:633", "Brachydactyly - preaxial hallux varus": "Orphanet:1278", "eye morphology measurement": "EFO:0007858", "Humerus trochlea aplasia": "Orphanet:3383", "Xeroderma pigmentosum": "Orphanet:910", "Constitutional neutropenia": "Orphanet:101987", "Peutz-Jeghers Polyp": "EFO:1000470", "Spinocerebellar ataxia type 6": "Orphanet:98758", "CLN10 disease": "Orphanet:228337", "WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement": "EFO:0008319", "Abnormality of the inner ear": "HP:0000359", "Partial duplication of chromosome 6": "Orphanet:262628", "GM17196 {http": "CLO:0013816", "Multiple epiphyseal dysplasia, Beighton type": "Orphanet:166011", "Kearns-Sayre syndrome": "Orphanet:480", "response to paclitaxel": "GO:1901555", "Early infantile epileptic encephalopathy without suppression burst": "Orphanet:369894", "diabetic nephropathy": "EFO:0000401", "Ulnar/fibula ray defect - brachydactyly": "Orphanet:52056", "Uk-2": "EFO:0005162", "1p36 deletion syndrome": "Orphanet:1606", "AA89": "EFO:0004027", "SLAM family member 7 measurement": "EFO:0008287", "Monosomy 18q": "Orphanet:1600", "Drosophila sechellia": "NCBITaxon:7238", "Metatropic dysplasia": "Orphanet:2635", "atrophic rhinitis": "EFO:0007159", "Polysyndactyly - cardiac malformation": "Orphanet:2934", "Venezuelan equine encephalitis": "EFO:0007534", "Hyperglycemia": "HP:0003074", "SUP-B15": "EFO:0006763", "Primary glomerular disease": "Orphanet:102373", "fetal hypoxia": "EFO:1001793", "airway hyperresponsiveness": "EFO:0005414", "HVA measurement": "EFO:0005131", "Naegeli-Franceschetti-Jadassohn syndrome": "Orphanet:69087", "vagal ganglion 4": "UBERON:2001305", "Zaire ebolavirus": "NCBITaxon:186538", "peritonitis": "EFO:0008588", "late rosette growth stage": "PO:0007076", "NUGC-3": "EFO:0006702", "transcription profiling by MPSS": "EFO:0002942", "amino acid measurement": "EFO:0005134", "Gossypium longicalyx": "NCBITaxon:34280", "ovarian cancer cell lines": "EFO:0002394", "Disorder of metabolite absorption and transport": "Orphanet:309824", "Inverse Marcus-Gunn phenomenon": "Orphanet:98951", "endoplasmic reticulum": "GO:0005783", "Umkirch ecotype": "EFO:0005160", "Cranioectodermal dysplasia": "Orphanet:1515", "Late-onset localized junctional epidermolysis bullosa - intellectual disability": "Orphanet:231556", "neuropeptide S": "CHEBI:53461", "endolymphatic hydrops": "EFO:1000918", "NAD-dependent protein deacetylase sirtuin-2 measurement": "EFO:0008241", "Congenital factor X deficiency": "Orphanet:328", "tinea favosa": "EFO:0007511", "T265": "EFO:0006304", "Odontohypophosphatasia": "Orphanet:247685", "Ataxia-telangiectasia-like disorder": "Orphanet:251347", "Cervical spina bifida aperta": "Orphanet:268392", "Dental enamel hypoplasia": "EFO:1001304", "Swiss2": "EFO:0006298", "Monosomy 5p": "Orphanet:281", "Proximal myotonic myopathy": "Orphanet:606", "eosinophil percentage of granulocytes": "EFO:0007996", "age-related hearing impairment": "EFO:0005782", "Spermophilus lateralis": "NCBITaxon:76772", "Atkin-Flaitz syndrome": "Orphanet:1193", "Spermophilus parryii": "NCBITaxon:9999", "Zonular cataract": "Orphanet:98995", "SF268": "EFO:0005451", "Carnitine palmitoyltransferase II deficiency": "Orphanet:157", "Odontomicronychial dysplasia": "Orphanet:1811", "mental or behavioural disorder": "EFO:0000677", "MOR": "EFO:0006655", "GM17292 {http": "CLO:0013136", "CS57858": "EFO:0000147", "Microcephalic primordial dwarfism due to ZNF335 deficiency": "Orphanet:329228", "Partial duplication of the short arm of chromosome 16": "Orphanet:262794", "Abnormality of sodium homeostasis": "HP:0010931", "Coimbra ecotype": "EFO:0005176", "sex interaction measurement": "EFO:0008343", "Familial temporal epilepsy": "Orphanet:98819", "Non-immunoglobulin-mediated membranoproliferative glomerulonephritis": "Orphanet:329918", "Gingival fibromatosis - progressive deafness": "Orphanet:2027", "Neonatal intrahepatic cholestasis due to citrin deficiency": "Orphanet:247598", "Methylobacterium extorquens": "NCBITaxon:408", "Oncorhynchus mykiss": "NCBITaxon:8022", "dissociation process": "EFO:0009091", "Joubert syndrome and related disorders": "Orphanet:140874", "Disseminated superficial actinic porokeratosis": "Orphanet:79152", "Rickettsia rickettsii": "NCBITaxon:783", "fruit size 30 to 50% stage {http": "PO:0025506", "Cardiospondylocarpofacial syndrome": "Orphanet:3238", "liver neoplasm": "EFO:1001513", "ventricular repolarisation duration measurement": "EFO:0008335", "Julidochromis transcriptus": "NCBITaxon:70784", "Syndactyly": "Orphanet:90025", "syntactic complexity measurement": "EFO:0007799", "peritoneum": "UBERON:0002358", "short physical performance battery score measurement": "EFO:0008454", "Eyelids malposition disorder": "Orphanet:98567", "ethanol": "CHEBI:16236", "fibrosis": "EFO:0006890", "Epidermal nevus syndrome": "Orphanet:35125", "response to wounding": "GO:0009611", "atmosphere": "EFO:0000273", "but-1-ene": "CHEBI:48362", "anterolateral myocardial infarction": "EFO:1000812", "Cerebellar ataxia - ectodermal dysplasia": "Orphanet:1174", "coronary atheroscleroris measurement": "EFO:0007938", "Hyperinsulinism due to HNF4A deficiency": "Orphanet:263455", "Spinocerebellar ataxia type 31": "Orphanet:217012", "Pontocerebellar hypoplasia type 1": "Orphanet:2254", "Fraction A pre-pro B cell": "CL:0002045", "alpha globulin measurement": "EFO:0004813", "SNU182": "EFO:0002345", "nervous system disease": "EFO:0000618", "SUM159PT": "EFO:0001241", "Escherichia coli B str. REL606": "NCBITaxon:413997", "Chordoid Meningioma": "EFO:1000176", "48,XXXY syndrome": "Orphanet:96263", "fibular nerve {http": "UBERON:0035652", "Lactobacillus sakei": "NCBITaxon:1599", "Genetic visceral malformation of the liver, biliary tract, pancreas or spleen": "Orphanet:183548", "interleukin-8 measurement": "EFO:0004811", "TMEM165-CDG": "Orphanet:314667", "Radio-ulnar synostosis - amegakaryocytic thrombocytopenia": "Orphanet:71289", "Keratinopathic ichthyosis": "Orphanet:281103", "Herpesvirus saimiri (strain 11)": "NCBITaxon:10383", "5-hydroxymethyl-2-furoic acid {http": "CHEBI:89118", "gamma-Glu-Glu {http": "CHEBI:73705", "hemoglobin A1 measurement": "EFO:0007629", "Alnus glutinosa": "NCBITaxon:3517", "FA6": "EFO:0006392", "Hoyeraal-Hreidarsson syndrome": "Orphanet:3322", "surgical shock": "EFO:0007686", "superoxide dismutase [Mn], mitochondrial measurement": "EFO:0008294", "Renal coloboma syndrome": "Orphanet:1475", "telomere": "EFO:0004359", "Atypical Meningioma": "EFO:1000101", "suicide behaviour": "EFO:0007623", "Sarcophilus harrisii": "NCBITaxon:9305", "SURF1-related Charcot-Marie-Tooth disease type 4": "Orphanet:391351", "granulocyte monocyte progenitor cell": "CL:0000557", "Marginal papular palmoplantar keratoderma": "Orphanet:307995", "Inability to walk {http": "HP:0002540", "Vaginal Adenoid Cystic Carcinoma": "EFO:1000617", "Multiple endocrine neoplasia type 2A": "Orphanet:247698", "glycosyl compound biosynthetic process": "GO:1901659", "mitochondrial intermembrane space": "GO:0005758", "Microcephaly - glomerulonephritis - marfanoid habitus": "Orphanet:2172", "Choroidal atrophy - alopecia": "Orphanet:1433", "HCT8": "EFO:0002189", "folic acid measurement": "EFO:0005111", "Acroosteolysis-keloid-like lesions-premature aging syndrome": "Orphanet:363665", "angioimmunoblastic T-cell lymphoma": "EFO:0000255", "Localized junctional epidermolysis bullosa, non-Herlitz type": "Orphanet:251393", "ObOb": "EFO:0002747", "Systemic primary carnitine deficiency": "Orphanet:158", "atrial myocardium": "UBERON:0002302", "Congenital pulmonary lymphangiectasia": "Orphanet:2414", "GM17282 {http": "CLO:0013094", "AREDYLD syndrome": "Orphanet:1133", "neutral ceramidase measurement": "EFO:0008247", "Secretory diarrhea": "HP:0005208", "SW527": "EFO:0005462", "decreased susceptibility to bacterial infection": "EFO:0008322", "Osteopetrosis - hypogammaglobulinemia": "Orphanet:178389", "Palpebral tumor with a vascular malformation": "Orphanet:98592", "embryonic gonadal ridge": "EFO:0001414", "superior mesenteric artery syndrome": "EFO:1001201", "Say-Field-Coldwell syndrome": "Orphanet:3133", "sialic acid-binding Ig-like lectin 14 measurement": "EFO:0008284", "Symptomatic form of hemophilia A in female carriers": "Orphanet:177926", "Hispanic": "EFO:0003169", "Mitochondrial membrane transport disorder": "Orphanet:254827", "Streptomyces lividans": "NCBITaxon:1916", "Charcot-Marie-Tooth disease type 1A": "Orphanet:101081", "response to risperidone": "GO:0097336", "Psammomatous Meningioma": "EFO:1000500", "Tularemia": "EFO:1001444", "Intellectual disability, severe {http": "HP:0010864", "LS1034": "EFO:0002226", "fruit size up to 10% stage {http": "PO:0025504", "BTBR mouse": "EFO:0002522", "Abnormality of the large intestine": "HP:0002250", "coenzyme": "CHEBI:23354", "CD34-positive, CD41-positive, CD42-negative megakaryocyte progenitor cell": "CL:0002025", "Spinocerebellar ataxia type 27": "Orphanet:98764", "Thermosynechococcus elongatus BP-1": "NCBITaxon:197221", "Mycobacterium avium": "NCBITaxon:1764", "Retinal cavernous hemangioma": "Orphanet:71213", "Autosomal dominant cerebellar ataxia": "Orphanet:99", "Spinal muscular atrophy - Dandy-Walker malformation - cataracts": "Orphanet:73245", "Infantile spams - psychomotor retardation - progressive brain atrophy - basal ganglia disease": "Orphanet:263410", "Heart neoplasm": "EFO:1001339", "protein N-linked glycosylation": "GO:0006487", "carotid artery central pulse pressure measurement": "EFO:0007721", "LAM-HTGTS": "EFO:0008784", "Venous thrombosis": "HP:0004936", "N-octylhomovanillamide": "CHEBI:64041", "3-hydroxy-3-methylglutarate(1-) {http": "CHEBI:30920", "mating type F": "EFO:0004012", "anti-topoisomerase-I-antibody-positive systemic scleroderma": "EFO:0008537", "immature NK T cell": "CL:0000914", "HC11": "EFO:0006414", "Bdellovibrio bacteriovorus": "NCBITaxon:959", "Epinephelus tauvina": "NCBITaxon:203262", "KPL-4": "EFO:0006624", "Congenital elbow dislocation, unilateral": "Orphanet:295225", "embryonic ventral apodeme": "FBbt:00005749", "CHARGE syndrome": "Orphanet:138", "cortex of kidney": "UBERON:0001225", "Autosomal dominant myoglobinuria": "Orphanet:99846", "high throughput sequence alignment protocol": "EFO:0004917", "CCD-13Lu": "EFO:0005361", "has extra parts of type": "PATO:0002002", "Non-hereditary late-onset primary lymphedema": "Orphanet:90185", "Hyperparathyroidism-jaw tumor syndrome": "Orphanet:99880", "Qualitative or quantitative defects of myotubularin": "Orphanet:207110", "desmoplastic medulloblastoma": "EFO:0005699", "selenite(2-)": "CHEBI:18212", "Kit-positive, integrin beta7-high basophil mast progenitor cell": "CL:0002044", "ulcer of lower limb": "EFO:0007068", "localised scleroderma": "EFO:1001361", "NCI-H1563": "EFO:0002255", "echinostomiasis": "EFO:0007246", "1-fluoro-2,4-dinitrobenzene": "CHEBI:53049", "signet ring cell carcinoma": "EFO:0000698", "conduct disorder": "EFO:0004216", "seed {http": "PO:0009010", "splenic white pulp macrophage": "CL:0000876", "Rare otorhinolaryngological malformation": "Orphanet:96333", "ulcerative proctosigmoiditis": "EFO:1001223", "gastrulating embryo Ce": "EFO:0005503", "Multiple epiphyseal dysplasia type 1": "Orphanet:93308", "methylmalonic aciduria and homocystinuria type cblG": "EFO:0005597", "multinuclear odontoclast": "CL:0000780", "Mutilating palmoplantar keratoderma with periorificial keratotic plaques": "Orphanet:659", "Phakomatosis spilorosea": "Orphanet:79485", "Myoclonic-astastic epilepsy": "Orphanet:1942", "1-linoleoyl-sn-glycero-3-phosphoethanolamine {http": "CHEBI:83058", "Disease predisposing to age-related macular degeneration": "Orphanet:98667", "Double outlet right ventricle with non-committed subpulmonary ventricular septal defect": "Orphanet:99046", "Malus x domestica": "NCBITaxon:3750", "Lower limb deficiency - hypospadias": "Orphanet:2487", "JRT3T35": "EFO:0002213", "GM17746 {http": "CLO:0016566", "basal ganglia cerebrovascular disease": "EFO:1000640", "Atypical pantothenate kinase-associated neurodegeneration": "Orphanet:216873", "Leptosphaeria maculans": "NCBITaxon:5022", "radiation unit": "UO:0000127", "Periapical Periodontitis": "EFO:1001391", "Nystagmus": "HP:0000639", "susceptibility to common cold measurement": "EFO:0008417", "Obesity due to CEP19 deficiency": "Orphanet:397615", "cerebellar hemisphere": "UBERON:0002245", "Leigh syndrome with leukodystrophy": "Orphanet:255241", "abnormality of metabolism/homeostasis": "HP:0001939", "Respirovirus infectious disease": "EFO:0007465", "Sertoli cell": "CL:0000216", "excitatory amino acid agonist": "CHEBI:50103", "bis(2-chloroethyl) sulfide": "CHEBI:25434", "Craniodigital syndrome - intellectual disability": "Orphanet:1514", "nonepidermolytic palmoplantar keratoderma": "EFO:1000743", "Brachydactyly type A7": "Orphanet:93397", "postpoliomyelitis syndrome": "EFO:0007454", "beta-carotene measurement": "EFO:0007894", "Hyperornithinemia-hyperammonemia-homocitrullinuria": "Orphanet:415", "Streptomyces maritimus": "NCBITaxon:115828", "MIA Paca-2": "EFO:0002236", "Lactobacillus hilgardii": "NCBITaxon:1588", "Canthal anomaly": "Orphanet:98572", "Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA": "Orphanet:254776", "Genetic vascular anomaly": "Orphanet:211240", "NCI-H209": "EFO:0006671", "intestinal volvulus": "EFO:1000989", "CD34-positive, CD38-negative hematopoietic stem cell": "CL:0001024", "stroke": "EFO:0000712", "COLO 699": "EFO:0006374", "Spinocerebellar ataxia type 1": "Orphanet:98755", "Glaucoma - ectopia - microspherophakia - stiff joints - short stature": "Orphanet:2084", "insulin resistance": "EFO:0002614", "meningoencephalitis": "EFO:0007364", "Testicular regression syndrome": "Orphanet:983", "MINCE-seq": "EFO:0008812", "HEK-293 cell": "BTO:0000007", "Genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability": "Orphanet:330206", "Succinyl-CoA": "Orphanet:832", "Encephalopathy due to GLUT1 deficiency": "Orphanet:71277", "OVCA429": "EFO:0006721", "FVB/NJ": "EFO:0007728", "supraorbital lateral line neuromast": "UBERON:2001026", "Craniosynostosis, Philadelphia type": "Orphanet:1527", "Autosomal dominant focal dystonia, DYT7 type": "Orphanet:93963", "meningeal neoplasm": "EFO:0003851", "Angiomyxoma": "EFO:1000087", "Tetranychus urticae": "NCBITaxon:32264", "Silver-Russell syndrome due to a point mutation": "Orphanet:397590", "hybrid selection of targets": "EFO:0004188", "OE21": "EFO:0002309", "Craniodiaphyseal dysplasia": "Orphanet:1513", "food allergy measurement": "EFO:0007016", "Dolichocephaly {http": "HP:0000268", "hypohidrosis": "EFO:1000712", "eWGA": "EFO:0008733", "HCC2935": "EFO:0005375", "Gitelman syndrome": "Orphanet:358", "Alopecia totalis": "Orphanet:700", "Bull's eye maculopathy {http": "HP:0011504", "Micrococcal Nuclease digestion": "EFO:0004177", "heartwater disease": "EFO:1000960", "Lysosomal disease with hypertrophic cardiomyopathy": "Orphanet:217581", "Juvenile absence epilepsy": "Orphanet:1941", "osteoblast": "CL:0000062", "leucine {http": "CHEBI:25017", "Tendinopathy": "EFO:1001434", "Multiple endocrine neoplasia type 2B": "Orphanet:247709", "actinomycin D": "CHEBI:27666", "Borderline Ovarian Endometrioid Tumor": "EFO:1000137", "base unit": "UO:0000045", "dental phobia": "EFO:1001884", "magnesium sulfate {http": "CHEBI:32599", "cerebrospinal fluid": "UBERON:0001359", "Tetraodon nigroviridis": "NCBITaxon:99883", "lacrimal gland": "UBERON:0001817", "PEO1": "EFO:0005445", "Autosomal recessive cerebellar ataxia - saccadic intrusion": "Orphanet:95434", "GM17262 {http": "CLO:0013173", "uterine cervix": "UBERON:0000002", "Conjunctival lymphangiectasia": "Orphanet:98614", "lung cancer cell": "BTO:0000551", "Marinesco-Sj\u00c3\u00b6gren syndrome": "Orphanet:559", "Disorder of zinc metabolism": "Orphanet:309845", "topoisomerase I inhibitor": "CHEBI:50276", "Isolated congenital sclerocornea": "Orphanet:91490", "GM19239": "EFO:0002789", "Cleft lip/palate - ectodermal dysplasia": "Orphanet:320317", "anterior pancreatic bud": "ZFA:0001369", "GM17247 {http": "CLO:0014417", "Renal Angiomyoadenomatous Tumor": "EFO:1000507", "trabecular meshwork": "EFO:0003077", "sulpiride": "CHEBI:32168", "Immunoglobulin-mediated membranoproliferative glomerulonephritis": "Orphanet:329903", "BT20": "EFO:0001092", "bone giant cell tumor": "EFO:0007176", "Familial restrictive cardiomyopathy": "Orphanet:217635", "grip strength measurement": "EFO:0006941", "mid whole plant fruit ripening stage {http": "PO:0007031", "XYLT1-CDG": "Orphanet:370930", "Brachydactyly type C": "Orphanet:93384", "Familial episodic pain syndrome with predominantly upper body involvement": "Orphanet:391389", "Citrobacter rodentium": "NCBITaxon:67825", "alpha-methyl-L-tyrosine": "CHEBI:6912", "epilepsy": "EFO:0000474", "dihomo-gamma-linoleic acid measurement": "EFO:0008356", "SCIM": "EFO:0007030", "Acrodysostosis": "Orphanet:950", "M14": "EFO:0003056", "Wide nasal bridge {http": "HP:0000431", "Methanobacterium congolense": "NCBITaxon:118062", "Childhood-onset epilepsy syndrome": "Orphanet:98259", "erythrocyte": "CL:0000232", "nasal cavity squamous cell carcinoma": "EFO:1000057", "CD8-alpha-beta-positive, alpha-beta intraepithelial T cell": "CL:0000796", "lipoxin A4": "CHEBI:6498", "Mucopolysaccharidosis with skin involvement": "Orphanet:79388", "lung carcinoma": "EFO:0001071", "postsynaptic density": "GO:0014069", "Multiple epiphyseal dysplasia type 4": "Orphanet:93307", "feature extraction": "EFO:0000494", "A498": "EFO:0002105", "gene deletion library": "EFO:0007560", "SW620": "EFO:0002368", "response to water deprivation": "GO:0009414", "Distal hereditary motor neuropathy": "Orphanet:53739", "purine ribonucleoside triphosphate metabolic process": "GO:0009205", "Tessier number 4 facial cleft": "Orphanet:141258", "complement factor H-related protein 5 measurement": "EFO:0008098", "Akinesia {http": "HP:0002304", "lipoprotein measurement": "EFO:0004732", "melanotic neuroectodermal tumor": "EFO:1001038", "EB3": "EFO:0002174", "Foster-Kennedy syndrome": "EFO:1001330", "Combined immunodeficiency due to ZAP70 deficiency": "Orphanet:911", "plasma plasminogen measurement": "EFO:0006309", "reticulum cell sarcoma": "EFO:0005287", "Partial duplication of the short arm of chromosome 7": "Orphanet:262749", "Weaver-Williams syndrome": "Orphanet:3448", "adipose dendritic cell": "CL:0002462", "pollen tube": "EFO:0001004", "(+)-catechin monohydrate": "CHEBI:58994", "serum IgM measurement": "EFO:0004993", "Flock house virus": "NCBITaxon:12287", "chitin": "CHEBI:17029", "Lupus Vasculitis, Central Nervous System": "EFO:1001363", "Autosomal recessive spastic paraplegia type 39": "Orphanet:139480", "Ovine herpesvirus 2": "NCBITaxon:10398", "ND00397 {http": "CLO:0027048", "Rhodopirellula baltica": "NCBITaxon:265606", "Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis": "Orphanet:94062", "DN2 thymocyte": "CL:0000806", "coronary artery": "UBERON:0001621", "GM17107 {http": "CLO:0014903", "Cucumis melo": "NCBITaxon:3656", "HPDE6-E6E7": "EFO:0005711", "Phakomatosis with eye involvement": "Orphanet:98701", "Glutaric acidemia type 3": "Orphanet:35706", "slow muscle cell somite 7": "ZFA:0000973", "actinomycosis": "EFO:0007128", "tragus size": "EFO:0007668", "Combined oxidative phosphorylation defect type 30": "EFO:0009038", "Wyeomyia smithii": "NCBITaxon:174621", "Triticum aestivum cv. Chinese Spring": "EFO:0007588", "Circle-Seq": "EFO:0008689", "transitional cell papilloma": "EFO:0006497", "RWPE1": "EFO:0002323", "Pseudomonas {http": "NCBITaxon:286", "Sorsby's fundus dystrophy": "Orphanet:59181", "NCI-H727": "EFO:0006695", "CLN1 disease": "Orphanet:228329", "liter": "UO:0000099", "Parkes Weber syndrome": "Orphanet:90307", "Essential fructosuria": "Orphanet:2056", "Disorder of O-mannosylglycan synthesis": "Orphanet:309469", "left superior temporal gyrus grey matter volume measurement": "EFO:0007697", "hepatitis C infection": "EFO:0003047", "Bradyrhizobium japonicum": "NCBITaxon:375", "Bronchiolitis": "HP:0011950", "ileal neoplasm": "EFO:1000981", "urinary bladder fistula": "EFO:1001862", "5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamide": "CHEBI:18406", "gut microbiome measurement": "EFO:0007874", "BL-2 {http": "EFO:0005475", "Syndromic X-linked intellectual disability 7": "Orphanet:85274", "Testicular Yolk Sac Tumor": "EFO:1000574", "Mycobacterium tuberculosis CDC1551": "NCBITaxon:83331", "Central Nervous System Neoplasm": "EFO:1000158", "Limb dystonia": "Orphanet:93957", "SHOX-related short stature": "Orphanet:314795", "Trisomy 18p": "Orphanet:1715", "Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency": "Orphanet:331176", "Generalized junctional epidermolysis bullosa, non-Herlitz type": "Orphanet:79402", "fraction": "UO:0000191", "X-linked cleft palate and ankyloglossia": "Orphanet:324601", "diastolic heart failure": "EFO:1000899", "milligram per liter": "UO:0000273", "1,5 anhydroglucitol measurement": "EFO:0008009", "immunoproliferative small intestinal disease": "EFO:1001798", "dermal neurofibroma": "EFO:0000397", "family size": "EFO:0004802", "linolenic acid measurement": "EFO:0006811", "Puccinia graminis f. sp. tritici": "NCBITaxon:56615", "urocortin II": "EFO:0002680", "Autosomal dominant proximal renal tubular acidosis": "Orphanet:314889", "Lymphangioleiomyomatosis": "Orphanet:538", "2-hydroxy-3-methylbutyric acid {http": "CHEBI:60645", "Osteopetrosis with renal tubular acidosis": "Orphanet:2785", "mycosis fungoides": "EFO:1001051", "BDC2.5/NOD": "EFO:0001337", "Congenital absence of both lower leg and foot, bilateral": "Orphanet:295099", "colorectal neoplasm": "EFO:0004142", "adenohypophyseal placode": "UBERON:0009122", "rhombomere 3": "UBERON:0005507", "tolbutamide": "CHEBI:27999", "Isolated follicle stimulating hormone deficiency": "Orphanet:52901", "JT interval": "EFO:0007885", "Blue cone monochromatism": "Orphanet:16", "LC-1F": "EFO:0002827", "toxicodendron dermatitis": "EFO:1000773", "Poroma": "EFO:1001826", "Cyprinus carpio": "NCBITaxon:7962", "RC301": "EFO:0004059", "Premature aging appearance-developmental delay-cardiac arrhythmia syndrome": "Orphanet:276432", "diarrhea": "HP:0002014", "high grade ovarian serous adenocarcinoma": "EFO:1001958", "herpangina": "EFO:0007306", "Ichthyosis prematurity syndrome": "Orphanet:88621", "multinuclear osteoclast": "CL:0000779", "Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344": "NCBITaxon:216597", "GM12239": "EFO:0001144", "blood cell": "CL:0000081", "Pentasomy X": "Orphanet:11", "CCD-19Lu": "EFO:0005363", "RT4": "EFO:0006480", "blood aluminium measurement": "EFO:0007575", "Metabolic disease associated with ocular features": "Orphanet:98710", "bilirubin": "CHEBI:16990", "Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome": "Orphanet:401959", "congenital rubella": "EFO:0007218", "Guttmacher syndrome": "Orphanet:2957", "GM17110 {http": "CLO:0014964", "adrenal gland pheochromocytoma": "EFO:0000239", "Wagner disease": "Orphanet:898", "European HapMap cell line": "EFO:0004902", "corpus allatum": "UBERON:0001057", "Pierre Robin syndrome - faciodigital anomaly": "Orphanet:2888", "Abnormality of the liver": "HP:0001392", "survival time": "EFO:0000714", "SUPeR-seq": "EFO:0008956", "Syndromic neurometabolic disease with non-X-linked intellectual disability": "Orphanet:182073", "Cavernous Hemangioma": "EFO:1000151", "disease state design": "EFO:0001756", "Neuronal intestinal pseudoobstruction": "Orphanet:99811", "NCI-H1581": "EFO:0002257", "A549": "EFO:0001086", "Okamoto-Aoki": "EFO:0001348", "Streptococcus thermophilus": "NCBITaxon:1308", "gill filament": "UBERON:0009120", "T-WGBS": "EFO:0008957", "MS428": "EFO:0002837", "Isolated osteopoikilosis": "Orphanet:166119", "Ichthyosis - hepatosplenomegaly - cerebellar degeneration": "Orphanet:2274", "thiopurine methyltransferase activity measurement": "EFO:0007852", "jejunal cancer": "EFO:1000998", "Kit-low proerythroblast": "CL:0002012", "EEG with generalized epileptiform discharges {http": "HP:0011198", "Holoprosencephaly - craniosynostosis": "Orphanet:2163", "Suprabasal epidermolysis bullosa simplex": "Orphanet:158661", "Populus": "NCBITaxon:3689", "Zygodactyly type 3": "Orphanet:295191", "matrix metalloproteinase measurement": "EFO:0004744", "Isaacs syndrome": "EFO:1000638", "Bifidobacterium breve": "NCBITaxon:1685", "mesenteric vascular occlusion": "EFO:1001043", "Punctate palmoplantar keratoderma type 1": "Orphanet:79501", "Atypical juvenile parkinsonism": "Orphanet:391411", "Brassica carinata x Brassica rapa {http": "NCBITaxon:1324865", "Gynatresia": "EFO:1001335", "Pelizaeus-Merzbacher-like disease": "Orphanet:280270", "Amelo-onycho-hypohidrotic syndrome": "Orphanet:1028", "YCC10": "EFO:0002877", "Craniosynostosis": "Orphanet:1531", "gastrointestinal hemorrhage": "HP:0002239", "Posterior meningocele": "Orphanet:268810", "sodium hydroxide": "CHEBI:32145", "T2 B cell": "CL:0000959", "ILSXISS52/TejJ": "EFO:0002988", "fetomaternal transfusion": "EFO:1001794", "Barber-Say syndrome": "Orphanet:1231", "immature CD8_alpha-positive CD11b-negative dendritic cell": "CL:0001004", "artificial sequences": "NCBITaxon:81077", "Hypereosinophilic syndrome": "EFO:1001467", "Non-distal monosomy 20q": "Orphanet:96164", "Ovarian hyperstimulation syndrome": "Orphanet:64739", "acute synovitis": "EFO:0008998", "influenza": "EFO:0007328", "cryptoxanthin measurement": "EFO:0007897", "Tomato ringspot virus": "NCBITaxon:12280", "ornithine carbamoyltransferase deficiency": "EFO:0007409", "anlage in statu nascendi": "UBERON:6005413", "Cutaneous T-cell lymphoma": "EFO:0002913", "Congenital absence/hypoplasia of thumb": "Orphanet:294988", "wild type genotype": "EFO:0005168", "Hereditary angioedema type 1": "Orphanet:100050", "Familial congenital palsy of trochlear nerve": "Orphanet:91498", "Sabia virus": "NCBITaxon:45709", "oxalate(2-) {http": "CHEBI:30623", "Andropogon gerardii": "NCBITaxon:79824", "ILSXISS19/TejJ": "EFO:0002977", "C3 glomerulonephritis": "Orphanet:329931", "stomach": "UBERON:0000945", "Synpolydactyly type 3": "Orphanet:295199", "Thymic Carcinoma": "EFO:1000576", "zinc ion homeostasis": "GO:0055069", "plantar wart": "EFO:1002023", "adenosine 5'-monophosphate {http": "CHEBI:16027", "Erdheim-Chester disease": "EFO:1000926", "abnormality of body weight": "HP:0004323", "Splenic Mantle Cell Lymphoma": "EFO:1000549", "Non-acquired combined pituitary hormone deficiency with spine abnormalities": "Orphanet:231720", "pharyngeal pouches 2-6": "UBERON:2001129", "AB SOLiD System 3.0": "EFO:0004439", "Atypical hemolytic-uremic syndrome with I factor anomaly": "Orphanet:93580", "hexadecanoate {http": "CHEBI:7896", "submandibular gland": "UBERON:0001736", "GM17280 {http": "CLO:0013096", "Calyptogena magnifica symbiont": "NCBITaxon:2361", "Autosomal recessive cerebellar ataxia": "Orphanet:1172", "sweat gland disease": "EFO:1000772", "Goodman syndrome": "Orphanet:65798", "perphenazine": "CHEBI:8028", "Familial isolated arrhythmogenic ventricular dysplasia, right dominant form": "Orphanet:293910", "Persistent hyperplastic primary vitreous": "Orphanet:91495", "Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys": "Orphanet:79118", "Childhood encephalopathy due to thiamine pyrophosphokinase deficiency": "Orphanet:293955", "folic acid reductase inhibitor": "CHEBI:50683", "carotid artery circumferential wall stress measurement": "EFO:0007724", "visceral muscle primordium": "FBbt:00005519", "QRS duration": "EFO:0005055", "peritrophic membrane": "BTO:0001038", "Mosaic trisomy 3": "Orphanet:100071", "Partial deletion of the long arm of chromosome 18": "Orphanet:262146", "NOD mouse": "EFO:0002547", "Ba-1": "EFO:0007606", "GM17296 {http": "CLO:0013124", "Aym\u00c3\u00a9-Gripp syndrome": "EFO:0009020", "having extra processual parts": "PATO:0001561", "GM07348 {http": "CLO:0016951", "colorectal carcinoma": "EFO:1001951", "potassium deficiency": "EFO:1001120", "Lenz-Majewski hyperostotic dwarfism": "Orphanet:2658", "mature neutrophil": "CL:0000096", "cervical artery dissection": "EFO:1000059", "bronchiolitis obliterans": "EFO:0007183", "lymphangiectasis": "EFO:1001025", "dopaminergic neuron": "CL:0000700", "congenital disorder of glycosylation type I": "EFO:0005545", "cellular modification design": "EFO:0004666", "Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly": "Orphanet:98694", "Rare constitutional hemolytic anemia": "Orphanet:182043", "inflammatory response": "GO:0006954", "Spinocerebellar ataxia type 23": "Orphanet:101108", "Beemer-Ertbruggen syndrome": "Orphanet:1237", "Severe lateral tibial bowing with short stature": "Orphanet:324307", "normalization data transformation": "OBI:0200169", "Fraction B precursor B cell": "CL:0002047", "Mononen-Karnes-Senac syndrome": "Orphanet:2565", "Mayetiola destructor": "NCBITaxon:39758", "Familial partial lipodystrophy, K\u00c3\u00b6bberling type": "Orphanet:79084", "Brachydactyly of toes, unilateral": "Orphanet:295132", "Hereditary sensory and autonomic neuropathy with deafness and global delay": "Orphanet:139573", "NOD.B6": "EFO:0002745", "Primary familial polycythemia": "Orphanet:90042", "X-linked Charcot-Marie-Tooth disease type 6": "Orphanet:352675", "calcineurin": "CHEBI:53439", "Peripheral resistance to thyroid hormones": "Orphanet:97927", "Distal renal tubular acidosis with anemia": "Orphanet:93610", "temporal measurement": "EFO:0000719", "fungal-type cell wall": "GO:0009277", "Charcot-Marie-Tooth disease type 4B3": "Orphanet:363981", "beriberi": "EFO:1000837", "elementary body": "BTO:0000377", "Legionella longbeachae": "NCBITaxon:450", "Severe early-onset axonal neuropathy due to NEFL deficiency": "Orphanet:228374", "GM17122 {http": "CLO:0015117", "Autosomal recessive syndromic cerebellar ataxia": "Orphanet:98099", "Rare hereditary neurologic disease with peripheral neuropathy": "Orphanet:207025", "46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency": "Orphanet:168558", "Glycogen storage disease with hypertrophic cardiomyopathy": "Orphanet:217572", "Rabies virus": "NCBITaxon:11292", "myeloid leukocyte": "CL:0000766", "Distal monosomy 7p": "Orphanet:96126", "Pt45P1": "EFO:0002716", "aortic aneurysm": "EFO:0001666", "ChIRP": "EFO:0008687", "HCC44": "EFO:0003133", "Short palpebral fissure {http": "HP:0012745", "Abruptio Placentae": "EFO:1001754", "transforming growth factor beta measurement": "EFO:0004818", "Goldenhar syndrome": "Orphanet:374", "Shoulder and thorax deformity - congenital heart disease": "Orphanet:1940", "Fusarium acuminatum": "NCBITaxon:502705", "HCA-7": "EFO:0006415", "HCC1359": "EFO:0003128", "eye infection": "EFO:1001888", "X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - Seizures": "Orphanet:1568", "Hypertonia {http": "HP:0001276", "tacrolimus hydrate": "CHEBI:61057", "Diastematomyelia": "Orphanet:1671", "Leymus cinereus": "NCBITaxon:86020", "urethral neoplasm": "EFO:0003846", "Familial progressive hyperpigmentation": "Orphanet:79146", "GM14679 {http": "CLO:0031953", "Retinal dystrophy": "Orphanet:71862", "hip circumference": "EFO:0005093", "Monosomy 21": "Orphanet:574", "thoracic aorta": "UBERON:0001515", "Combined pancreatic lipase-colipase deficiency": "Orphanet:309111", "MALT lymphoma": "EFO:0000191", "Camptodactyly syndrome, Guadalajara type 2": "Orphanet:1326", "Coloboma of macula": "Orphanet:98945", "Theiler stage 27": "EFO:0004391", "Naumovozyma": "NCBITaxon:278028", "cot filtration for theoretical single copy genomic DNA": "EFO:0004174", "Amelogenesis imperfecta": "Orphanet:88661", "Muscle-eye-brain disease": "Orphanet:588", "Hemoglobin D disease": "Orphanet:90039", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C": "Orphanet:308400", "sapropterin dihydrochloride": "CHEBI:32120", "Lipoic acid biosynthesis defect": "Orphanet:401854", "nylon substrate": "EFO:0005063", "pericardium": "UBERON:0002407", "SCL-exo": "EFO:0008909", "autoimmune bullous skin disease": "EFO:0008598", "adult onset asthma": "EFO:1002011", "Cryopyrin-associated periodic syndrome": "Orphanet:208650", "N-methylnicotinate {http": "CHEBI:18123", "Metaphyseal dysplasia, Braun-Tinschert type": "Orphanet:85188", "telencephalic ventricle {http": "UBERON:0002285", "Disorder of porphyrin and haem metabolism": "Orphanet:309813", "Lattice corneal dystrophy type I": "Orphanet:98964", "4q21 microdeletion syndrome": "Orphanet:238750", "L-proline": "CHEBI:17203", "Allan-Herndon-Dudley syndrome": "Orphanet:59", "dietary heme iron intake measurement": "EFO:0008355", "floor plate of midbrain": "UBERON:0003307", "middRAD": "EFO:0008810", "Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy": "Orphanet:156156", "EGF-like module-containing mucin-like hormone receptor-like 2 measurement": "EFO:0008116", "Spinocerebellar ataxia type 43": "EFO:0009060", "cardinal organ part {http": "PO:0025001", "basophilic myeloblast": "CL:0000829", "Glutaric aciduria": "HP:0003150", "Sparse and thin eyebrow {http": "HP:0000535", "Autosomal dominant hyperinsulinism due to SUR1 deficiency": "Orphanet:276575", "GM17251 {http": "CLO:0014391", "hatching long-pec": "EFO:0002718", "Microtriplication 11q24.1": "Orphanet:289522", "Lethal arteriopathy syndrome due to fibulin-4 deficiency": "Orphanet:314718", "Nail-patella syndrome": "Orphanet:2614", "vacuole": "GO:0005773", "Niemann-Pick disease type C, juvenile neurologic onset": "Orphanet:216981", "Muenke syndrome": "Orphanet:53271", "hair cell anterior macula": "ZFA:0000678", "Geobacter sulfurreducens PCA": "NCBITaxon:243231", "Congenital macroglossia": "Orphanet:2430", "guard cell": "CL:0000292", "Pfeiffer syndrome type 1": "Orphanet:93258", "Anopheles gambiae": "NCBITaxon:7165", "synophrys measurement": "EFO:0007906", "HTGTS": "EFO:0008770", "aldosterone-producing adenoma": "EFO:1000015", "plant ovule": "PO:0020003", "pancreatic bud": "UBERON:0003922", "Epidermolysis bullosa simplex, Ogna type": "Orphanet:79401", "Pontocerebellar hypoplasia type 4": "Orphanet:166063", "Craniosynostosis and dental anomalies": "Orphanet:284149", "homostachydrine {http": "CHEBI:5757", "Classic multiminicore myopathy": "Orphanet:324604", "Non progressive epilepsy and/or ataxia with myoclonus as a major feature": "Orphanet:306759", "cups of coffee per day measurement": "EFO:0006782", "skin pigmentation measurement": "EFO:0007009", "biliverdin {http": "CHEBI:17033", "Neuroblastic Tumor": "EFO:1000393", "Genetic 46,XY disorder of sex development of endocrine origin": "Orphanet:325713", "dermatographia": "EFO:1000685", "causalgia": "EFO:1000854", "Borderline personality disorder": "HP:0012076", "Genetic polycythemia": "Orphanet:250165", "lung carcinoid tumor": "EFO:1000037", "3-aminobenzamide": "CHEBI:64042", "Actinobacillus pleuropneumoniae serovar 1 str. 4074": "NCBITaxon:228399", "whole plant fruit formation stage 70% to final size {http": "PO:0007027", "protein jagged-1 measurement": "EFO:0008271", "derived unit": "UO:0000046", "X-ChIP-seq": "EFO:0008986", "seasonality measurement": "EFO:0006876", "Posterior polymorphous corneal dystrophy": "Orphanet:98973", "GM09581 {http": "CLO:0011436", "Renier-Gabreels-Jasper syndrome": "Orphanet:93975", "tyrosine measurement": "EFO:0005058", "Phlebotomus fever": "EFO:0007437", "Clear Cell Papillary Cystadenoma": "EFO:1000181", "Pseudomonas aeruginosa": "NCBITaxon:287", "Primary erythermalgia": "Orphanet:90026", "Laryngeal dyskinesia": "Orphanet:93961", "Parana hard-skin syndrome": "Orphanet:2812", "KM12": "EFO:0006282"};