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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-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
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Secondary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00407613989Dyskeratosis congenita, autosomal dominant, 21Show list of biomolecules +1
DI-00493162000Familial juvenile hyperuricemic nephropathy 11Show list of biomolecules +1
DI-00563614076Hermansky-Pudlak syndrome 71Show list of biomolecules +1
DI-00564614077Hermansky-Pudlak syndrome 81Show list of biomolecules +1
DI-00806606966Nephronophthisis 41Show 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-02080604901North American Indian childhood cirrhosis1Show list of biomolecules +1
DI-02259208540Renal-hepatic-pancreatic dysplasia 11Show list of biomolecules +1
DI-02901613159Nephronophthisis-like nephropathy 11Show 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-03187614171Hermansky-Pudlak syndrome 91Show list of biomolecules +1
DI-03387614480Hypertriglyceridemia, transient infantile1Show list of biomolecules +1
DI-03843615382Nephronophthisis 161Show list of biomolecules +1
DI-03895615438Infantile liver failure syndrome 11Show 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
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