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  Diseases matching the query *Fibrosis* and the corresponding human biomolecules involved in at least one interaction

Primary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00352135700Fibrosis of extraocular muscles, congenital, 11Show list of biomolecules +1
DI-01466219700Cystic fibrosis1Show list of biomolecules +1
DI-02509600638Fibrosis of extraocular muscles, congenital, 3A1Show list of biomolecules +1
DI-02670178500Pulmonary fibrosis, idiopathic3Show list of biomolecules +3
DI-02746254450Myelofibrosis1Show list of biomolecules +1
DI-03415254450Myelofibrosis with myeloid metaplasia1Show list of biomolecules +1
DI-03500614742Pulmonary fibrosis, and/or bone marrow failure, telomere-related, 11Show list of biomolecules +1
DI-04431616373Pulmonary fibrosis, and/or bone marrow failure, telomere-related, 31Show list of biomolecules +1
DI-04987617441Thrombocytopenia, anemia, and myelofibrosis1Show list of biomolecules +1
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Secondary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00407613989Dyskeratosis congenita, autosomal dominant, 21Show list of biomolecules +1
DI-00408224230Dyskeratosis congenita, autosomal recessive, 11Show list of biomolecules +1
DI-00493162000Familial juvenile hyperuricemic nephropathy 11Show list of biomolecules +1
DI-00530613027Glycogen storage disease 9C1Show list of biomolecules +1
DI-00558608233Hermansky-Pudlak syndrome 21Show list of biomolecules +1
DI-00560614073Hermansky-Pudlak syndrome 41Show list of biomolecules +1
DI-00561614074Hermansky-Pudlak syndrome 51Show list of biomolecules +1
DI-00563614076Hermansky-Pudlak syndrome 71Show list of biomolecules +1
DI-00564614077Hermansky-Pudlak syndrome 81Show list of biomolecules +1
DI-00799605814Cholestasis, neonatal intrahepatic, caused by citrin deficiency1Show list of biomolecules +1
DI-00806606966Nephronophthisis 41Show list of biomolecules +1
DI-00950601847Cholestasis, progressive familial intrahepatic, 21Show list of biomolecules +1
DI-01301166700Buschke-Ollendorff syndrome1Show list of biomolecules +1
DI-01313208250Camptodactyly-arthropathy-coxa vara-pericarditis syndrome1Show list of biomolecules +1
DI-01389277180Congenital bilateral absence of the vas deferens1Show list of biomolecules +1
DI-01454215600Cirrhosis2Show list of biomolecules +2
DI-01707235550Hepatic venoocclusive disease with immunodeficiency1Show list of biomolecules +1
DI-02002255320Multiminicore disease with external ophthalmoplegia1Show list of biomolecules +1
DI-02031610199Diabetes mellitus, neonatal, with congenital hypothyroidism1Show list of biomolecules +1
DI-02259208540Renal-hepatic-pancreatic dysplasia 11Show list of biomolecules +1
DI-02715218330Cranioectodermal dysplasia 11Show list of biomolecules +1
DI-02835216360COACH syndrome3Show list of biomolecules +3
DI-02898613550Nephronophthisis 111Show list of biomolecules +1
DI-02901613159Nephronophthisis-like nephropathy 11Show list of biomolecules +1
DI-03050613824Nephronophthisis 91Show list of biomolecules +1
DI-03051613820Nephronophthisis 121Show list of biomolecules +1
DI-03165613990Dyskeratosis congenita, autosomal dominant, 31Show list of biomolecules +1
DI-03166613989Dyskeratosis congenita, autosomal recessive, 41Show list of biomolecules +1
DI-03167613987Dyskeratosis congenita, autosomal recessive, 21Show list of biomolecules +1
DI-03168613988Dyskeratosis congenita, autosomal recessive, 31Show list of biomolecules +1
DI-03183614099Cranioectodermal dysplasia 31Show list of biomolecules +1
DI-03187614171Hermansky-Pudlak syndrome 91Show list of biomolecules +1
DI-03326614377Nephronophthisis 131Show list of biomolecules +1
DI-03327614378Cranioectodermal dysplasia 41Show list of biomolecules +1
DI-03387614480Hypertriglyceridemia, transient infantile1Show list of biomolecules +1
DI-03475266920Short-rib thoracic dysplasia 9 with or without polydactyly1Show list of biomolecules +1
DI-03547614844Nephronophthisis 141Show list of biomolecules +1
DI-03755615190Dyskeratosis congenita, autosomal recessive, 51Show list of biomolecules +1
DI-03843615382Nephronophthisis 161Show list of biomolecules +1
DI-03889615190Dyskeratosis congenita, autosomal dominant, 41Show list of biomolecules +1
DI-03891615415Renal-hepatic-pancreatic dysplasia 21Show list of biomolecules +1
DI-03895615438Infantile liver failure syndrome 11Show list of biomolecules +1
DI-04019615636Joubert syndrome 211Show list of biomolecules +1
DI-04152615878Cholestasis, progressive familial intrahepatic, 41Show list of biomolecules +1
DI-04336616217Nephronophthisis 191Show list of biomolecules +1
DI-04360616278Congenital bile acid synthesis defect 51Show list of biomolecules +1
DI-04521616553Dyskeratosis congenita, autosomal dominant, 61Show list of biomolecules +1
DI-04522616553Dyskeratosis congenita, autosomal recessive, 71Show list of biomolecules +1
DI-04550616483Infantile liver failure syndrome 21Show list of biomolecules +1
DI-04579616654Joubert syndrome 241Show list of biomolecules +1
DI-04603616719Spinocerebellar ataxia, autosomal recessive, 211Show list of biomolecules +1
DI-04607616781Joubert syndrome 251Show list of biomolecules +1
DI-04615616784Joubert syndrome 261Show list of biomolecules +1
DI-04653616818IgA nephropathy 31Show list of biomolecules +1
DI-04719616937Thrombocytopenia 61Show list of biomolecules +1
DI-04774617049Cholestasis, progressive familial intrahepatic, 51Show list of biomolecules +1
DI-04775617050Hermansky-Pudlak syndrome 101Show list of biomolecules +1
DI-04819617120Joubert syndrome 271Show list of biomolecules +1
DI-04820617121Joubert syndrome 281Show list of biomolecules +1
DI-04885617175Retinal dystrophy with or without extraocular anomalies1Show list of biomolecules +1
DI-04920617271Nephronophthisis 201Show list of biomolecules +1
DI-04970617394Sclerosing cholangitis, neonatal1Show list of biomolecules +1
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