{"orpha":79214,"name":"Disorder of biogenic amine metabolism and transport","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-79214/","orphanet_url":"https://www.orpha.net/en/disease/detail/79214","names":{"fr":{"name":"Trouble du métabolisme et du transport des amines biogènes"},"de":{"name":"Störung des Biogene Amine-Stoffwechsels/-Transports"},"es":{"name":"Enfermedad del metabolismo y transporte de aminas biogénicas"},"it":{"name":"Difetto del metabolismo e del trasporto delle ammine biogeniche"},"nl":{"name":"Stoornis van biogeen aminemetabolisme en -transport"},"pt":{"name":"Metabólica da neurotransmissão, anomalia"},"pl":{"name":"Zaburzenie metabolizmu i transportu amin biogennych"},"cs":{"name":"Poruchy metabolismu a transportu biogenních aminů"},"uk":{"name":"Порушення метаболізму та транспорту біогенних амінів"},"zh":{"name":"生物胺代谢和转运异常"},"tr":{"name":"Biyojenik amin metabolizması ve taşınmasında bozukluk"}},"xrefs":[{"source":"MONDO","code":"0019250","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19250","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681274","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":68367,"name":"Rare inborn error of metabolism","classifications":[150,156]}],"children":[{"orpha":79175,"name":"Disorder of gamma-aminobutyric acid metabolism","type":"Category"},{"orpha":79169,"name":"Disorder of neurotransmitter metabolism and transport","type":"Category"},{"orpha":79192,"name":"Disorder of pyridoxine metabolism","type":"Category"},{"orpha":79219,"name":"Metabolic disease involving other neurotransmitter deficiency","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}