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 |
| Adrenoleukodystrophy, neonatal | 0 |
| Alzheimer disease, familial | 0 |
| Amelogenesis imperfecta | 0 |
| Amyloidosis | 0 |
| Amyotrophic lateral sclerosis | 0 |
| Anophthalmia - Microphthalmia, isolated | 0 |
| Atrial fibrillation, familial | 0 |
| Atypical hemolytic uremic syndrome | 0 |
| Autosomal dominant Charcot-Marie-Tooth disease, type 2 | 0 |
| Autosomal dominant centronuclear myopathy | 0 |
| Autosomal dominant cerebellar ataxia | 0 |
| Autosomal recessive malignant osteopetrosis | 0 |
| Autosomal recessive spondylocostal dysostosis | 0 |
| Bardet-Biedl syndrome | 0 |
| Bartter syndrome | 0 |
| Beckwith-Wiedemann syndrome | 0 |
| Brachydactyly | 0 |
| Breast cancer, familial | 0 |
| COFS syndrome | 0 |
| Calcinosis, tumoral | 0 |
| Cardiofaciocutaneous syndrome | 0 |
| Cardiomyopathy, familial dilated | 0 |
| Cardiomyopathy, hypertrophic, primary or idiopathic | 0 |
| Cataract, cerulean | 0 |
| Cataract, posterior polar | 0 |
| Cataract, pulverulent | 0 |
| Cataract, zonular | 0 |
| Centronuclear myopathy | 0 |
| Charcot-Marie-Tooth disease, type 1 | 0 |
| Classic Ehlers-Danlos syndrome | 0 |
| Cleft lip with or without cleft palate | 0 |
| Colon cancer, familial nonpolyposis | 0 |
| Cone rod dystrophy | 0 |
| Congenital adrenal hyperplasia | 0 |
| Congenital myasthenic syndromes | 0 |
| Conotruncal heart malformations | 0 |
| Corneal dystrophy | 0 |
| Crohn disease | 0 |
| Cutis laxa | 0 |
| Deafness, autosomal dominant, nonsyndromic, sensorineural, type DFNA | 0 |
| Deafness, autosomal recessive, nonsyndromic, sensorineural, type DFNB | 0 |
| Dejerine-Sottas syndrome | 0 |
| Emery-Dreifuss muscular dystrophy | 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 |
| Fanconi anemia | 0 |
| Frontotemporal dementia | 0 |
| Generalized epilepsy with febrile seizures-plus context | 0 |
| Glaucoma, hereditary | 0 |
| Glioblastoma | 0 |
| Gonadal dysgenesis, XY female type | 0 |
| Granulomatous disease, chronic | 0 |
| Hemochromatosis | 0 |
| Hereditary pheochromocytoma-paraganglioma syndrome | 0 |
| Hermansky-Pudlak syndrome | 0 |
| Heterotaxia | 0 |
| Hirschsprung disease | 0 |
| Holoprosencephaly | 0 |
| Hyper-IgM syndrome | 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 |
| Joubert syndrome | 0 |
| Juvenile myoclonic epilepsy | 0 |
| Kallmann syndrome | 0 |
| Late infantile neuronal ceroid lipofuscinosis | 0 |
| Leber amaurosis, congenital | 0 |
| Leukemia, lymphoblastic, acute | 0 |
| Leukemia, myeloid, acute | 0 |
| Long QT syndrome, familial | 0 |
| MALT lymphoma | 0 |
| Meckel syndrome | 0 |
| Medullary cystic kidney disease, autosomal recessive | 0 |
| Medulloblastoma | 0 |
| Mendelian susceptibility to atypical mycobacteria | 0 |
| Mild nemaline myopathy | 0 |
| Mitochondrial DNA depletion syndrome | 0 |
| Mucopolysaccharidosis type 3 | 0 |
| Multiple pterygium syndrome, lethal form | 0 |
| Nemaline myopathy | 0 |
| Neural tube defect | 0 |
| Neuronal ceroid lipofuscinosis | 0 |
| Night blindness, stationary, congenital | 0 |
| Non-syndromic congenital cataract | 0 |
| Nonacquired combined pituitary hormone deficiency | 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 |
| Pachyonychia congenita | 0 |
| Pancreatic carcinoma, familial | 0 |
| Parkinson disease, genetic type | 0 |
| Pelizaeus-Merzbacher disease | 0 |
| Peters anomaly | 0 |
| Porphyria | 0 |
| Postsynaptic congenital myasthenic syndromes | 0 |
| Prader-Willi syndrome | 0 |
| Premature ovarian failure | 0 |
| Primary ciliary dyskinesia | 0 |
| Primary familial polycythemia | 0 |
| Progressive cone dystrophy | 0 |
| Progressive external ophthalmoplegia | 0 |
| Prostate cancer, familial | 0 |
| Pseudohypoaldosteronism, type 1 | 0 |
| Pulmonary alveolar proteinosis | 0 |
| Rare intellectual deficit without developmental anomaly | 0 |
| Renal tubular dysgenesis | 0 |
| Retinitis pigmentosa | 0 |
| Senior-Loken syndrome | 0 |
| Silver-Russell syndrome | 0 |
| Situs ambiguus | 0 |
| Spherocytosis hereditary | 0 |
| Spondyloepimetaphyseal dysplasia | 0 |
| Spondyloepiphyseal dysplasia | 0 |
| Stickler syndrome | 0 |
| Tetralogy of Fallot | 0 |
| Thoracic aortic aneurysm, familial form | 0 |
| Transposition of the great arteries | 0 |
| Transposition of the great arteries, right | 0 |
| Usher syndrome | 0 |
| Vitamin D resistant rickets | 0 |
| Walker-Warburg syndrome | 0 |
| Xeroderma pigmentosum | 0 |
| Zellweger syndrome | 0 |
| Bile acid synthesis defect with cholestasis and malabsorption | 1 |
| Diabetes mellitus, neonatal | 1 |
| Diabetes mellitus, neonatal, permanent | 1 |
| Hereditary chronic pancreatitis | 1 |
| Hypercholesterolemia, familial | 1 |
| MODY syndrome | 1 |
| Major hypertriglyceridemia | 1 |
| Persistent hyperinsulinemic hypoglycemia of infancy | 1 |
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)
