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 |
| Amyloid nephropathy, familial | 0 |
| Amyloidosis | 0 |
| Amyotrophic lateral sclerosis | 0 |
| Arrhythmogenic right ventricular dysplasia | 0 |
| Atrial fibrillation, familial | 0 |
| Atypical hemolytic uremic syndrome | 0 |
| Autism | 0 |
| Autoimmune lymphoproliferative syndrome | 0 |
| Autosomal dominant cerebellar ataxia | 0 |
| Bardet-Biedl syndrome | 0 |
| Bartter syndrome | 0 |
| Bile acid synthesis defect with cholestasis and malabsorption | 0 |
| Blackfan-Diamond disease | 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, pulverulent | 0 |
| Classic Ehlers-Danlos syndrome | 0 |
| Cleft lip with or without cleft palate | 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 |
| Corneal dystrophy | 0 |
| Cree leukoencephalopathy | 0 |
| Crigler-Najjar syndrome | 0 |
| Cutis laxa | 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 |
| 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 |
| 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 |
| Graesbeck-Imerslund disease | 0 |
| Granulomatous disease, chronic | 0 |
| Hemochromatosis | 0 |
| Hereditary pheochromocytoma-paraganglioma syndrome | 0 |
| Hermansky-Pudlak syndrome | 0 |
| Hirschsprung disease | 0 |
| Holoprosencephaly | 0 |
| Hyperbilirubinemia transient familial neonatal | 0 |
| Hypercholesterolemia, familial | 0 |
| Hyperekplexia, hereditary | 0 |
| Ichthyosis, lamellar | 0 |
| Idiopathic aplastic anemia | 0 |
| Iminoglycinuria | 0 |
| Immunodeficiency with a complement cascade protein anomaly | 0 |
| Interauricular communication | 0 |
| Joubert syndrome | 0 |
| Juvenile myoclonic epilepsy | 0 |
| Juvenile or adult CACH syndrome | 0 |
| Late infantile CACH syndrome | 0 |
| Late infantile neuronal ceroid lipofuscinosis | 0 |
| Leber amaurosis, congenital | 0 |
| Leigh syndrome | 0 |
| Leucinosis | 0 |
| Leukemia, lymphoblastic, acute | 0 |
| Leukemia, myeloid, acute | 0 |
| Leukemia, promyelocytic, acute | 0 |
| Long QT syndrome, familial | 0 |
| MALT lymphoma | 0 |
| MODY syndrome | 0 |
| Macular degeneration, age-related | 0 |
| Major hypertriglyceridemia | 0 |
| Meckel syndrome | 0 |
| Medulloblastoma | 0 |
| Mendelian susceptibility to atypical mycobacteria | 0 |
| Microcephaly, isolated congenital | 0 |
| Mild nemaline myopathy | 0 |
| Mitochondrial DNA depletion syndrome | 0 |
| Monilethrix | 0 |
| Mucopolysaccharidosis type 3 | 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 |
| Nonacquired combined pituitary hormone deficiency | 0 |
| Nonsyndromic genetic deafness | 0 |
| Noonan syndrome | 0 |
| Oculocutaneous albinism | 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 |
| Pontocerebellar hypoplasia | 0 |
| Porphyria | 0 |
| Postsynaptic congenital myasthenic syndromes | 0 |
| Prader-Willi syndrome | 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 |
| Pyruvate dehydrogenase deficiency | 0 |
| Refsum disease, infantile form | 0 |
| Renal cell carcinoma, familial | 0 |
| Renal tubular dysgenesis | 0 |
| Retinitis pigmentosa | 0 |
| Senior-Loken syndrome | 0 |
| Sheldon-Hall syndrome | 0 |
| Spherocytosis hereditary | 0 |
| Spondyloepimetaphyseal dysplasia | 0 |
| Spondyloepiphyseal dysplasia | 0 |
| Stickler syndrome | 0 |
| Thoracic aortic aneurysm, familial form | 0 |
| Usher syndrome | 0 |
| Walker-Warburg syndrome | 0 |
| Xeroderma pigmentosum | 0 |
| Zellweger syndrome | 0 |
| Transposition of the great arteries | 1 |
| Transposition of the great arteries, right | 1 |
| Encephalopathy due to sulfite oxidase deficiency | 2 |
| Xanthinuria | 2 |
| Charcot-Marie-Tooth disease, type 1 | 3 |
| Dejerine-Sottas syndrome | 3 |
| Gonadal dysgenesis, XY female type | 4 |
| Premature ovarian failure | 4 |
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)
