{"orpha":156601,"name":"Rare genetic hepatic disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-156601/","orphanet_url":"https://www.orpha.net/en/disease/detail/156601","names":{"fr":{"name":"Maladie hépatique génétique rare"},"de":{"name":"Leberkrankheit, genetische, seltene"},"es":{"name":"Enfermedades hepáticas genéticas raras"},"it":{"name":"Malattia epatica genetica"},"nl":{"name":"Zeldzame genetische leverziekte","synonyms":["Zeldzame genetische aandoening van lever"]},"pt":{"name":"Doença hepática genética"},"pl":{"name":"Rzadka genetyczna choroba wątroby"},"cs":{"name":"Vzácná geneticky podmíněná onemocnění jater"},"uk":{"name":"Рідкісне генетично обумовлене захворювання печінки"},"zh":{"name":"罕见遗传性肝病"},"tr":{"name":"Nadir genetik karaciğer hastalığı"}},"xrefs":[{"source":"MONDO","code":"15507","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680645","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":57146,"name":"Rare hepatic disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":1414,"name":"Cholestasis-lymphedema syndrome","type":"Disease"},{"orpha":156607,"name":"Genetic biliary tract disease","type":"Category"},{"orpha":156604,"name":"Genetic parenchymatous liver disease","type":"Category"},{"orpha":79124,"name":"Hepatic veno-occlusive disease-immunodeficiency syndrome","type":"Disease"},{"orpha":276405,"name":"Hyperbiliverdinemia","type":"Disease"},{"orpha":101940,"name":"Rare metabolic liver disease","type":"Category"},{"orpha":2312,"name":"Transient familial neonatal hyperbilirubinemia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}