{"orpha":289098,"name":"Disorders of vitamin D 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-289098/","orphanet_url":"https://www.orpha.net/en/disease/detail/289098","names":{"fr":{"name":"Troubles du métabolisme de la vitamine D"},"de":{"name":"Störung des Vitamin D-Stoffwechels"},"es":{"name":"Trastorno del metabolismo de la vitamina D"},"it":{"name":"Difetti del metabolismo della vitamina D"},"nl":{"name":"Stoornissen van vitamine D-metabolisme"},"pt":{"name":"Doenças do metabolismo da vitamina D"},"pl":{"name":"Zaburzenia metabolizmu witaminy D"},"cs":{"name":"Poruchy metabolismu vitaminu D"},"uk":{"name":"Порушення обміну вітаміну D"},"zh":{"name":"维生素D代谢紊乱"},"tr":{"name":"D vitamini metabolizması bozuklukları"}},"xrefs":[{"source":"MONDO","code":"0017322","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17322","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681017","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":93447,"name":"Primary bone dysplasia with defective bone mineralization","classifications":[147,156,199]},{"orpha":183634,"name":"Rare genetic parathyroid disease and phosphocalcic metabolism disorder","classifications":[156]},{"orpha":68415,"name":"Rare parathyroid disease and phosphocalcic metabolism anomaly","classifications":[193]}],"children":[{"orpha":289103,"name":"Hypocalcemic rickets","type":"Clinical group"},{"orpha":437,"name":"Hypophosphatemic rickets","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}