{"orpha":101939,"name":"Rare parenchymal liver 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-101939/","orphanet_url":"https://www.orpha.net/en/disease/detail/101939","names":{"fr":{"name":"Maladie rare du parenchyme hépatique"},"de":{"name":"Parenchymatöse Leberkrankheit, seltene"},"es":{"name":"Enfermedad hepática parenquimatosa rara"},"it":{"name":"Malattia epatica parenchimatosa rara"},"nl":{"name":"Zeldzame parenchymateuze leverziekte"},"pt":{"name":"Doença parenquimatosa hepática, rara"},"pl":{"name":"Rzadkie choroby miąższu wątroby"},"cs":{"name":"Vzácné parenchymatózní onemocnění jater"},"uk":{"name":"Рідкісні паренхіматозні захворювання печінки"},"zh":{"name":"罕见实质性肝病"},"tr":{"name":"Nadir parankimal karaciğer hastalığı"}},"xrefs":[{"source":"MONDO","code":"15114","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681787","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19789","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":464682,"name":"OBSOLETE: Disorder with acute infantile liver failure","status":"inactive"}],"preferential_parent":{"orpha":57146,"name":"Rare hepatic disease"},"parents":[{"orpha":57146,"name":"Rare hepatic disease","classifications":[183]}],"children":[{"orpha":243367,"name":"Acute fatty liver of pregnancy","type":"Disease"},{"orpha":217371,"name":"Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins","type":"Disease"},{"orpha":466794,"name":"Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","type":"Disease"},{"orpha":370088,"name":"Acute infantile liver failure-multisystemic involvement syndrome","type":"Disease"},{"orpha":2137,"name":"Autoimmune hepatitis","type":"Disease"},{"orpha":731,"name":"Autosomal recessive polycystic kidney disease","type":"Disease"},{"orpha":397922,"name":"Ferro-cerebro-cutaneous syndrome","type":"Disease"},{"orpha":464724,"name":"Fever-associated acute infantile liver failure syndrome","type":"Disease"},{"orpha":699068,"name":"Fontan-associated liver disease","type":"Disease"},{"orpha":35063,"name":"Fulminant viral hepatitis","type":"Disease"},{"orpha":541423,"name":"Growth delay-intellectual disability-hepatopathy syndrome","type":"Disease"},{"orpha":391366,"name":"Growth retardation-mild developmental delay-chronic hepatitis syndrome","type":"Disease"},{"orpha":2031,"name":"Hepatic fibrosis-renal cysts-intellectual disability syndrome","type":"Malformation syndrome"},{"orpha":726824,"name":"Hepatorenocardiac degenerative fibrosis","type":"Disease"},{"orpha":209919,"name":"Idiopathic copper-associated cirrhosis","type":"Disease"},{"orpha":90003,"name":"Inflammatory pseudotumor of the liver","type":"Disease"},{"orpha":69665,"name":"Intrahepatic cholestasis of pregnancy","type":"Disease"},{"orpha":485426,"name":"Isolated congenital hepatic fibrosis","type":"Disease"},{"orpha":1454,"name":"Joubert syndrome with hepatic defect","type":"Clinical subtype"},{"orpha":3032,"name":"NPHP3-related Meckel-like syndrome","type":"Malformation syndrome"},{"orpha":562639,"name":"Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome","type":"Disease"},{"orpha":210136,"name":"Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome","type":"Disease"},{"orpha":294415,"name":"Renal-hepatic-pancreatic dysplasia","type":"Malformation syndrome"},{"orpha":440427,"name":"Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency","type":"Disease"},{"orpha":300293,"name":"Transient infantile hypertriglyceridemia and hepatosteatosis","type":"Disease"},{"orpha":84064,"name":"Trichohepatoenteric syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}