{"orpha":309833,"name":"Disorder of other vitamins and cofactors 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-309833/","orphanet_url":"https://www.orpha.net/en/disease/detail/309833","names":{"fr":{"name":"Anomalie du métabolisme et du transport des autres vitamines et cofacteurs"},"de":{"name":"Weitere Vitamin- und Kofaktor-Stoffwechsel- und Transportstörungen"},"es":{"name":"Trastornos del metabolismo y transporte de otras vitaminas y cofactores"},"it":{"name":"Difetto del trasporto e del metabolismo delle altre vitamine e dei cofattori"},"nl":{"name":"Stoornis van andere vitaminen en cofactoren-metabolisme en transport"},"pt":{"name":"Alteração de outras vitaminas e cofatores do metabolismo e transporte"},"pl":{"name":"Zaburzenia metabolizmu i transportu innych witamin i kofaktorów"},"cs":{"name":"Poruchy metabolismu a transportu jiných vitaminů a kofaktorů"},"uk":{"name":"Порушення метаболізму та транспорту інших вітамінів і кофакторів"},"zh":{"name":"其他维生素和辅助因子代谢-转运障碍"},"tr":{"name":"Diğer vitamin ve kofaktör metabolizması ve taşınmasında bozukluk"}},"xrefs":[{"source":"MONDO","code":"17760","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681036","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":309827,"name":"Disorder of vitamin and non-protein cofactor absorption and transport","classifications":[150,156]}],"children":[{"orpha":96,"name":"Ataxia with vitamin E deficiency","type":"Disease"},{"orpha":79241,"name":"Biotinidase deficiency","type":"Disease"},{"orpha":98434,"name":"Hereditary combined deficiency of vitamin K-dependent clotting factors","type":"Disease"},{"orpha":199285,"name":"Hereditary hypercarotenemia and vitamin A deficiency","type":"Disease"},{"orpha":79242,"name":"Holocarboxylase synthetase deficiency","type":"Disease"},{"orpha":411712,"name":"Maternal riboflavin deficiency","type":"Disease"},{"orpha":157850,"name":"Pantothenate kinase-associated neurodegeneration","type":"Disease"},{"orpha":352718,"name":"Progressive retinal dystrophy due to retinol transport defect","type":"Disease"},{"orpha":79096,"name":"Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy","type":"Disease"},{"orpha":521268,"name":"Sodium-dependent multivitamin transporter deficiency","type":"Disease"},{"orpha":99732,"name":"Sulfite oxidase deficiency due to molybdenum cofactor deficiency","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}