{"orpha":352728,"name":"Disorder of melanin metabolism","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-352728/","orphanet_url":"https://www.orpha.net/en/disease/detail/352728","names":{"fr":{"name":"Trouble du métabolisme de la mélanine"},"de":{"name":"Melanin-Stoffwechselstörung"},"es":{"name":"Trastorno del metabolismo de la melanina"},"it":{"name":"Difetto del metabolismo della melanina"},"nl":{"name":"Stoornis van melaninemetabolisme"},"pt":{"name":"Alteração do metabolismo da melanina"},"pl":{"name":"Zaburzenia metabolizmu melaniny"},"cs":{"name":"Porucha metabolismu melaninu"},"uk":{"name":"Порушення обміну меланіну"},"zh":{"name":"黑色素代谢紊乱"},"tr":{"name":"Melanin metabolizması bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0018134","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"18134","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680988","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79062,"name":"Disorder of amino acid and other organic acid metabolism","classifications":[150,156]}],"children":[{"orpha":284804,"name":"Ocular albinism","type":"Clinical group"},{"orpha":55,"name":"Oculocutaneous albinism","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}