Orphan disease network

Orphan diseases network

7. Diseases network - Most connected diseases, edge as shared cellular component

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
Adrenoleukodystrophy, neonatal0
Alzheimer disease, familial0
Amelogenesis imperfecta0
Amyloid nephropathy, familial0
Amyotrophic lateral sclerosis0
Arrhythmogenic right ventricular dysplasia0
Atrial fibrillation, familial0
Atypical hemolytic uremic syndrome0
Autoimmune lymphoproliferative syndrome0
Autosomal dominant cerebellar ataxia0
Bardet-Biedl syndrome0
Bartter syndrome0
Bile acid synthesis defect with cholestasis and malabsorption0
Blackfan-Diamond disease0
Breast cancer, familial0
CACH syndrome0
COFS syndrome0
Cardiofaciocutaneous syndrome0
Cardiomyopathy, familial dilated0
Cardiomyopathy, hypertrophic, primary or idiopathic0
Cataract, pulverulent0
Classic Ehlers-Danlos syndrome0
Cleft lip with or without cleft palate0
Coenzyme Q cytochrome c reductase deficiency0
Colon cancer, familial nonpolyposis0
Cone rod dystrophy0
Congenital adrenal hyperplasia0
Congenital myasthenic syndromes0
Congenital or early infantile CACH syndrome0
Corneal dystrophy0
Cree leukoencephalopathy0
Crigler-Najjar syndrome0
Cutis laxa0
Deafness, autosomal dominant, nonsyndromic, sensorineural, type DFNA0
Deafness, autosomal recessive, nonsyndromic, sensorineural, type DFNB0
Diabetes mellitus, neonatal0
Diabetes mellitus, neonatal, permanent0
Dyskeratosis congenita0
Emery-Dreifuss muscular dystrophy0
Epidermolysis bullosa, epidermolytic0
Epidermolysis bullosa, generalized atrophic benign0
Epidermolysis bullosa, junctional0
Epidermolysis bullosa, junctional, non-Herlitz type0
Epiphyseal dysplasia multiple0
Erythroderma, congenital ichthyosiform, nonbullous0
Fanconi anemia0
Fatal infantile cytochrome C oxidase deficiency0
Frontotemporal dementia0
Generalized epilepsy with febrile seizures-plus context0
Gilbert syndrome0
Glutaryl-CoA dehydrogenase deficiency0
Graesbeck-Imerslund disease0
Granulomatous disease, chronic0
Hereditary pheochromocytoma-paraganglioma syndrome0
Hermansky-Pudlak syndrome0
Hirschsprung disease0
Hyperbilirubinemia transient familial neonatal0
Hypercholesterolemia, familial0
Hyperekplexia, hereditary0
Ichthyosis, lamellar0
Idiopathic aplastic anemia0
Immunodeficiency with a complement cascade protein anomaly0
Interauricular communication0
Joubert syndrome0
Juvenile myoclonic epilepsy0
Juvenile or adult CACH syndrome0
Late infantile CACH syndrome0
Late infantile neuronal ceroid lipofuscinosis0
Leber amaurosis, congenital0
Leigh syndrome0
Leukemia, lymphoblastic, acute0
Leukemia, myeloid, acute0
Leukemia, promyelocytic, acute0
Long QT syndrome, familial0
MALT lymphoma0
MODY syndrome0
Macular degeneration, age-related0
Major hypertriglyceridemia0
Meckel syndrome0
Mendelian susceptibility to atypical mycobacteria0
Microcephaly, isolated congenital0
Mild nemaline myopathy0
Mitochondrial DNA depletion syndrome0
Mucopolysaccharidosis type 30
Multiple pterygium syndrome, lethal form0
NADH-CoQ reductase deficiency0
Nemaline myopathy0
Neural tube defect0
Neuronal ceroid lipofuscinosis0
Night blindness, stationary, congenital0
Non-syndromic congenital cataract0
Nonacquired combined pituitary hormone deficiency0
Nonsyndromic genetic deafness0
Noonan syndrome0
Oculocutaneous albinism0
Osteogenesis imperfecta0
Pachyonychia congenita0
Pancreatic carcinoma, familial0
Parkinson disease, genetic type0
Pelizaeus-Merzbacher disease0
Persistent hyperinsulinemic hypoglycemia of infancy0
Peters anomaly0
Pontocerebellar hypoplasia0
Postsynaptic congenital myasthenic syndromes0
Prader-Willi syndrome0
Primary ciliary dyskinesia0
Primary familial polycythemia0
Progressive cone dystrophy0
Progressive external ophthalmoplegia0
Prostate cancer, familial0
Pseudohypoaldosteronism, type 10
Pyruvate dehydrogenase deficiency0
Refsum disease, infantile form0
Renal cell carcinoma, familial0
Renal tubular dysgenesis0
Retinitis pigmentosa0
Senior-Loken syndrome0
Sheldon-Hall syndrome0
Spherocytosis hereditary0
Spondyloepimetaphyseal dysplasia0
Spondyloepiphyseal dysplasia0
Stickler syndrome0
Thoracic aortic aneurysm, familial form0
Usher syndrome0
Walker-Warburg syndrome0
Xeroderma pigmentosum0
Zellweger syndrome0
Transposition of the great arteries1
Transposition of the great arteries, right1
Encephalopathy due to sulfite oxidase deficiency2
Charcot-Marie-Tooth disease, type 13
Dejerine-Sottas syndrome3
Gonadal dysgenesis, XY female type4
Premature ovarian failure4

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)