{"orpha":79169,"name":"Disorder of neurotransmitter 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-79169/","orphanet_url":"https://www.orpha.net/en/disease/detail/79169","names":{"fr":{"name":"Trouble du métabolisme et du transport des neurotransmetteurs"},"de":{"name":"Störung des Neurotransmitter-Stoffwechsels/-Transports"},"es":{"name":"Trastorno del metabolismo y transporte de los neurotransmisores"},"it":{"name":"Difetto del metabolismo e del trasporto dei neurotrasmettitori"},"nl":{"name":"Stoornis van neurotransmittermetabolisme en -transport"},"pt":{"name":"Doença do metabolismo das aminas biogénicas"},"pl":{"name":"Zaburzenie metabolizmu i transportu neuroprzekaźników"},"cs":{"name":"Poruchy metabolismu a transportu neurotransmiterů"},"uk":{"name":"Порушення метаболізму та транспорту нейромедіаторів"},"zh":{"name":"神经递质代谢和转运异常"},"tr":{"name":"Nörotransmiter metabolizması ve taşınmasında bozukluk"}},"xrefs":[{"source":"MONDO","code":"0019219","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19219","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681289","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79214,"name":"Disorder of biogenic amine metabolism and transport","classifications":[150,156]}],"children":[{"orpha":352649,"name":"Brain dopamine-serotonin vesicular transport disease","type":"Disease"},{"orpha":309830,"name":"Disorder of catecholamine synthesis","type":"Category"},{"orpha":309819,"name":"Disorder of pterin metabolism","type":"Category"},{"orpha":727719,"name":"Monoamine oxidase A and monoamine oxidase B deficiency","type":"Disease"},{"orpha":3057,"name":"Monoamine oxidase A deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}