{"orpha":308993,"name":"Glycerol kinase deficiency","type":"Clinical group","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-308993/","orphanet_url":"https://www.orpha.net/en/disease/detail/308993","names":{"fr":{"name":"Déficit en glycérol kinase"},"de":{"name":"Glycerol-Kinase-Mangel"},"es":{"name":"Deficiencia de glicerol quinasa"},"it":{"name":"Deficit di glicerolo chinasi"},"nl":{"name":"Glycerolkinasedeficiëntie"},"pt":{"name":"Défice de glicerol quinase"},"pl":{"name":"Niedobór kinazy glicerolu"},"cs":{"name":"Deficit glycerolkinázy"},"uk":{"name":"Дефіцит гліцеролкінази"},"zh":{"name":"甘油激酶缺乏症"},"tr":{"name":"Gliserol kinaz eksikliği"}},"xrefs":[{"source":"MONDO","code":"10613","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0268418","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79179,"name":"Disorder of glycerol metabolism","classifications":[150,156]}],"children":[{"orpha":408,"name":"Isolated glycerol kinase deficiency","type":"Disease"},{"orpha":261476,"name":"Xp21 deletion syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}