{"orpha":659694,"name":"Hepatic porphyria","type":"Clinical group","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-659694/","orphanet_url":"https://www.orpha.net/en/disease/detail/659694","names":{"fr":{"name":"Porphyrie hépatique"},"de":{"name":"Hepatische Porphyrie"},"es":{"name":"Porfiria hepática"},"it":{"name":"Porfiria epatica"},"nl":{"name":"Hepatische porfyrie"},"pt":{"name":"Porfiria hepática"},"pl":{"name":"Porfiria wątrobowa"},"cs":{"name":"Jaterní porfyrie"},"uk":{"name":"Печінкова порфірія"}},"xrefs":[{"source":"MONDO","code":"2520","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0162533","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":95161,"name":"OBSOLETE: Chronic hepatic porphyria","status":"inactive"}],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":738,"name":"Porphyria","classifications":[150,156,187,188]},{"orpha":101940,"name":"Rare metabolic liver disease","classifications":[156,183]}],"children":[{"orpha":95157,"name":"Acute hepatic porphyria","type":"Clinical group"},{"orpha":659698,"name":"Hepatic cutaneous porphyria","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}