{"orpha":659698,"name":"Hepatic cutaneous 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-659698/","orphanet_url":"https://www.orpha.net/en/disease/detail/659698","names":{"fr":{"name":"Porphyrie cutanée hépatique"},"de":{"name":"Hepatische kutane Porphyrie"},"es":{"name":"Porfiria hepática cutánea"},"it":{"name":"Porfiria cutanea epatica"},"nl":{"name":"Hepatische cutane porfyrie"},"pt":{"name":"Porfiria cutânea hepática"},"pl":{"name":"Porfiria wątrobowo-skórna"},"cs":{"name":"Jaterní kožní porfyrie"},"uk":{"name":"Печінкова шкірна порфірія"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":659694,"name":"Hepatic porphyria","classifications":[150,156,183,187,188]}],"children":[{"orpha":101330,"name":"Porphyria cutanea tarda","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}