{"orpha":79190,"name":"Disorder of phenylalanin or tyrosine 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-79190/","orphanet_url":"https://www.orpha.net/en/disease/detail/79190","names":{"fr":{"name":"Trouble du métabolisme de la phénylalanine ou de la tyrosine"},"de":{"name":"Phenylalanin/Tyrosin-Stoffwechselstörung"},"es":{"name":"Enfermedad del metabolismo de la fenilalanina o tirosina"},"it":{"name":"Malattia del metabolismo della fenilalanina o tirosina"},"nl":{"name":"Stoornis van fenylalanine- of tyrosinemetabolisme"},"pt":{"name":"Doença do metabolismo da fenilalanina ou tirosina"},"pl":{"name":"Zaburzenie metabolizmu fenyloalaniny i tyrozyny"},"cs":{"name":"Poruchy metabolismu fenyalaninu a tyrosinu"},"uk":{"name":"Порушення обміну фенілаланіну або тирозину"},"zh":{"name":"苯丙氨酸或酪氨酸代谢异常"},"tr":{"name":"Fenilalanin veya tirozin metabolizması bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0019235","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19235","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681284","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":284814,"name":"Disorder of phenylalanine metabolism","type":"Category"},{"orpha":284818,"name":"Disorder of tyrosine metabolism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}