This table contains the exhaustive list of each orphan disease and the corresponding weakly connected component ID. You can explore any connected component by clicking on its ID, or start exploring by a specific node by clicking on its name.
Orphan diseases interactive list
| Disease name |
Connected component ID |
| Achromatopsia | 0 |
| Alzheimer disease, familial | 0 |
| Amyloid nephropathy, familial | 0 |
| Amyloidosis | 0 |
| Autoimmune lymphoproliferative syndrome | 0 |
| Autosomal dominant cerebellar ataxia | 0 |
| Autosomal recessive malignant osteopetrosis | 0 |
| Autosomal recessive spondylocostal dysostosis | 0 |
| Bile acid synthesis defect with cholestasis and malabsorption | 0 |
| Blackfan-Diamond disease | 0 |
| Brachydactyly | 0 |
| Breast cancer, familial | 0 |
| CACH syndrome | 0 |
| COFS syndrome | 0 |
| Cardiofaciocutaneous syndrome | 0 |
| Cardiomyopathy, familial dilated | 0 |
| Cardiomyopathy, hypertrophic, primary or idiopathic | 0 |
| Cataract, cerulean | 0 |
| Cataract, pulverulent | 0 |
| Cataract, zonular | 0 |
| Chromosome Y deletion | 0 |
| Classic Ehlers-Danlos syndrome | 0 |
| Coenzyme Q cytochrome c reductase deficiency | 0 |
| Colon cancer, familial nonpolyposis | 0 |
| Cone rod dystrophy | 0 |
| Congenital adrenal hyperplasia | 0 |
| Congenital myasthenic syndromes | 0 |
| Congenital or early infantile CACH syndrome | 0 |
| Conotruncal heart malformations | 0 |
| Cree leukoencephalopathy | 0 |
| Crigler-Najjar syndrome | 0 |
| Crohn disease | 0 |
| Deafness, autosomal dominant, nonsyndromic, sensorineural, type DFNA | 0 |
| Deafness, autosomal recessive, nonsyndromic, sensorineural, type DFNB | 0 |
| Diabetes mellitus, neonatal | 0 |
| Diabetes mellitus, neonatal, permanent | 0 |
| Dyskeratosis congenita | 0 |
| Emery-Dreifuss muscular dystrophy | 0 |
| Encephalopathy due to sulfite oxidase deficiency | 0 |
| Epidermolysis bullosa, epidermolytic | 0 |
| Epidermolysis bullosa, generalized atrophic benign | 0 |
| Epidermolysis bullosa, junctional | 0 |
| Epidermolysis bullosa, junctional, non-Herlitz type | 0 |
| Epiphyseal dysplasia multiple | 0 |
| Erythroderma, congenital ichthyosiform, nonbullous | 0 |
| Ewing sarcoma | 0 |
| Fanconi anemia | 0 |
| Fatal infantile cytochrome C oxidase deficiency | 0 |
| Frontotemporal dementia | 0 |
| Generalized epilepsy with febrile seizures-plus context | 0 |
| Gilbert syndrome | 0 |
| Glioblastoma | 0 |
| Glutaryl-CoA dehydrogenase deficiency | 0 |
| Gonadal dysgenesis, XY female type | 0 |
| Graesbeck-Imerslund disease | 0 |
| Hereditary chronic pancreatitis | 0 |
| Hereditary pheochromocytoma-paraganglioma syndrome | 0 |
| Heterotaxia | 0 |
| Hirschsprung disease | 0 |
| Holoprosencephaly | 0 |
| Hyper-IgM syndrome | 0 |
| Hyperbilirubinemia transient familial neonatal | 0 |
| Hypercholesterolemia, familial | 0 |
| Hyperekplexia, hereditary | 0 |
| Hypodontia | 0 |
| Hypothyroidism, congenital | 0 |
| Ichthyosis, lamellar | 0 |
| Idiopathic aplastic anemia | 0 |
| Immunodeficiency by defective expression of HLA class 2 | 0 |
| Interauricular communication | 0 |
| Juvenile myoclonic epilepsy | 0 |
| Juvenile or adult CACH syndrome | 0 |
| Kallmann syndrome | 0 |
| Late infantile CACH syndrome | 0 |
| Leber amaurosis, congenital | 0 |
| Leigh syndrome | 0 |
| Leucinosis | 0 |
| Leukemia, promyelocytic, acute | 0 |
| MALT lymphoma | 0 |
| MODY syndrome | 0 |
| Macular degeneration, age-related | 0 |
| Major hypertriglyceridemia | 0 |
| Medulloblastoma | 0 |
| Mendelian susceptibility to atypical mycobacteria | 0 |
| Microcephaly, isolated congenital | 0 |
| Mild nemaline myopathy | 0 |
| Mitochondrial DNA depletion syndrome | 0 |
| Monosomy 22q11 | 0 |
| Multiple pterygium syndrome, lethal form | 0 |
| NADH-CoQ reductase deficiency | 0 |
| Nemaline myopathy | 0 |
| Neural tube defect | 0 |
| Neuronal ceroid lipofuscinosis | 0 |
| Night blindness, stationary, congenital | 0 |
| Non-syndromic congenital cataract | 0 |
| Nonsyndromic genetic deafness | 0 |
| Noonan syndrome | 0 |
| Normosmic congenital hypogonadotropic hypogonadism | 0 |
| Oculocutaneous albinism | 0 |
| Omenn syndrome | 0 |
| Ondine syndrome | 0 |
| Osteogenesis imperfecta | 0 |
| Ovarioleukodystrophy | 0 |
| Pachyonychia congenita | 0 |
| Pancreatic carcinoma, familial | 0 |
| Parkinson disease, genetic type | 0 |
| Pelizaeus-Merzbacher disease | 0 |
| Persistent hyperinsulinemic hypoglycemia of infancy | 0 |
| Peters anomaly | 0 |
| Polymicrogyria | 0 |
| Porphyria | 0 |
| Postsynaptic congenital myasthenic syndromes | 0 |
| Prader-Willi syndrome | 0 |
| Primary ciliary dyskinesia | 0 |
| Primary familial polycythemia | 0 |
| Progressive cone dystrophy | 0 |
| Prostate cancer, familial | 0 |
| Pulmonary alveolar proteinosis | 0 |
| Pyruvate dehydrogenase deficiency | 0 |
| Renal tubular dysgenesis | 0 |
| Retinitis pigmentosa | 0 |
| Sarcoidosis | 0 |
| Sheldon-Hall syndrome | 0 |
| Situs ambiguus | 0 |
| Spherocytosis hereditary | 0 |
| Spondyloepiphyseal dysplasia | 0 |
| Squamous cell carcinoma of head and neck | 0 |
| Stickler syndrome | 0 |
| Synovialosarcoma | 0 |
| Tetralogy of Fallot | 0 |
| Thoracic aortic aneurysm, familial form | 0 |
| Thyroid carcinoma, papillary or follicular | 0 |
| Transposition of the great arteries | 0 |
| Transposition of the great arteries, right | 0 |
| Xanthinuria | 0 |
| Xeroderma pigmentosum | 0 |
| Zellweger syndrome | 0 |
| Glaucoma, congenital | 1 |
| Glaucoma, hereditary | 1 |
| Beckwith-Wiedemann syndrome | 2 |
| Silver-Russell syndrome | 2 |
| Atypical hemolytic uremic syndrome | 3 |
| Immunodeficiency with a complement cascade protein anomaly | 3 |
The exploration is done with the Adobe Flash Web application GexfWalker. (Hint: find a specific orphan disease or related gene by searching it with the search feature of your web browser)
