{"orpha":156607,"name":"Genetic biliary tract 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-156607/","orphanet_url":"https://www.orpha.net/en/disease/detail/156607","names":{"fr":{"name":"Maladie génétique du tractus biliaire"},"de":{"name":"Gallengangkrankheit, genetisch bedingte"},"es":{"name":"Enfermedad genética del tracto biliar"},"it":{"name":"Malattia genetica del tratto biliare"},"nl":{"name":"Genetische galwegziekte"},"pt":{"name":"Doença do trato biliar, genética"},"pl":{"name":"Genetyczna choroba dróg żółciowych"},"cs":{"name":"Geneticky podmíněné nemoci žlučových cest"},"uk":{"name":"Генетично обумовлені захворювання жовчовивідних шляхів"},"zh":{"name":"遗传性胆道疾病"},"tr":{"name":"Genetik safra yolu hastalığı"}},"xrefs":[{"source":"MONDO","code":"15509","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680643","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":57146,"name":"Rare hepatic disease"},"parents":[{"orpha":156601,"name":"Rare genetic hepatic disease","classifications":[156]}],"children":[{"orpha":52,"name":"Alagille syndrome","type":"Malformation syndrome"},{"orpha":2697,"name":"Arthrogryposis-renal dysfunction-cholestasis syndrome","type":"Malformation syndrome"},{"orpha":53035,"name":"Caroli disease","type":"Malformation syndrome"},{"orpha":480520,"name":"Caroli syndrome","type":"Malformation syndrome"},{"orpha":521432,"name":"Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome","type":"Disease"},{"orpha":586,"name":"Cystic fibrosis","type":"Disease"},{"orpha":480556,"name":"Isolated neonatal sclerosing cholangitis","type":"Disease"},{"orpha":2924,"name":"Isolated polycystic liver disease","type":"Malformation syndrome"},{"orpha":69663,"name":"Low phospholipid-associated cholelithiasis","type":"Disease"},{"orpha":59303,"name":"Neonatal ichthyosis-sclerosing cholangitis syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}