{"orpha":35123,"name":"OBSOLETE: Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: 17b-hydroxysteroid dehydrogenase deficiency type 10","OBSOLETE: 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency","OBSOLETE: HSD deficiency"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency","url":"https://raremap.alftech.space/d/ORPHA-35123/","orphanet_url":"https://www.orpha.net/en/disease/detail/35123","names":{"fr":{"name":"OBSOLETE : Déficit en 3-hydroxyacyl-CoA déshydrogénase des acides gras à cha”ne courte","synonyms":["OBSOLETE : Déficit en 17b-hydroxystéroïde déshydrogénase type 10","OBSOLETE : Déficit en 2-méthyl-3-hydroxybutyryl-CoA déshydrogénase","OBSOLETE : Déficit en 3-hydroxy-2-méthylbutyryl-CoA déshydrogénase","OBSOLETE : Déficit en HSD","OBSOLETE : Déficit en MHBD","OBSOLETE : Déficit en SCHAD"]},"de":{"name":"OBSOLET: Kurzketten-3-Hydroxylacyl-CoA-Dehydrogenase-Mangel","synonyms":["OBSOLET: 17-beta-HSD-Mangel","OBSOLET: 2-Methyl-3-Hydroxybutyryl-CoA-Dehydrogenase-Mangel","OBSOLET: 3-Hydroxy-2-Methylbutyrat-CoA-Dehydrogenase-Mangel","OBSOLET: SCHAD-Mangel"]},"es":{"name":"OBSOLETO: Deficiencia de 3-hidroxiacil-CoA deshidrogenasa de cadena corta","synonyms":["OBSOLETO: Deficiencia de 17-b hidroxiesteroide deshidrogenasa tipo 10","OBSOLETO: Deficiencia de 3-hidroxi-2-methilbutiril-CoA deshidrogenasa","OBSOLETO: Deficiencia de HSD"]},"it":{"name":"OBSOLETO: Deficit di 3-idrossiacil-CoA deidrogenasi degli acidi grassi a catena corta","synonyms":["OBSOLETO: Deficit di 17b-idrossisteroido deidrogenasi, tipo 10","OBSOLETO: Deficit di 3-idrossi-2-metilbutirril-CoA deidrogenasi","OBSOLETO: Deficit di HSD"]},"nl":{"name":"OBSOLEET: Korte keten 3-hydroxyacyl-CoA-dehydrogenasedeficiëntie","synonyms":["OBSOLEET: 17-hydroxysteroïdedehydrogenasedeficiëntie type 10","OBSOLEET: 2-methyl-3-hydroxybutyryl-CoA-dehydrogenasedeficiëntie","OBSOLEET: 3-hydroxy-2-methylbutyryl-CoA-dehydrogenasedeficiëntie","OBSOLEET: HSD-deficiëntie","OBSOLEET: MHBD-deficiëntie","OBSOLEET: SCHAD-deficiëntie"]},"pt":{"name":"OBSOLETO: Deficiência de 3-hidroxilacil-CoA desidrogenase de cadeias curtas","synonyms":["OBSOLETO: Deficiência de 17b-hidroxisteróide desidrogenase tipo 10","OBSOLETO: Deficiência de 2-metil-3-hidroxibutiril-CoA desidrogenase","OBSOLETO: Deficiência de 3-hidroxi-2-metilbutiril-CoA desidrogenase","OBSOLETO: Deficiência de HSD","OBSOLETO: Deficiência de MHBD","OBSOLETO: Deficiência de SCHAD"]},"pl":{"name":"NIEAKTUALNE: Niedobór dehydrogenazy krótkolancuchowego 3-hydroksyacetylo-CoA","synonyms":["NIEAKTUALNE: 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency Niedobór dehydrogenazy 2-metylo - 3-hydroksybutyrylo-CoA","NIEAKTUALNE: Niedobór dehydrogenazy 17b-hydrosteroidowej typu 10","NIEAKTUALNE: Niedobór dehydrogenazy 3-hydroksy-3metylobutyrylo-CoA","NIEAKTUALNE: Niedobór HSD","NIEAKTUALNE: Niedobór MHBD","NIEAKTUALNE: Niedobór SCHAD"]},"cs":{"name":"NEAKTUÁLNÍ: Deficit 3-hydroxyacyl-CoA dehydrogenázy s krátkým řetězcem","synonyms":["OBSOLETE: 17b-hydroxysteroid dehydrogenase deficiency type 10","OBSOLETE: 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency","OBSOLETE: HSD deficiency"]},"uk":{"name":"ЗАСТАРІЛО: Дефіцит коротколанцюгової 3-гідроксиацил-КоА-дегідрогенази","synonyms":["ЗАСТАРІЛО: Дефіцит 17b-гідроксистероїддегідрогенази, тип 10","ЗАСТАРІЛО: Дефіцит 3-гідрокси-2-метилбутирил-КоА-дегідрогенази","ЗАСТАРІЛО: Недостатність HSD"]},"zh":{"name":"弃用：短链3-羟酰基辅酶A脱氢酶缺乏症","synonyms":["3-羟基-2-甲基丁酰辅酶A脱氢酶缺乏症"]},"tr":{"name":"Eski adı: Kısa zincirli 3-hidroksiasil-CoA dehidrogenaz eksikliği","synonyms":["HSD eksikliği","17b-hidroksisteroid dehidrojenaz eksikliği tip 10","3-hidroksi-2-metilbütiril-CoA dehidrojenaz eksikliği"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":71212,"name":"Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}