{"orpha":99763,"name":"OBSOLETE: Familial hyperreninemic hypoaldosteronism type 1","type":"Etiological subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: 18-hydroxylase deficiency","OBSOLETE: 18-oxidase deficiency","OBSOLETE: Aldosterone synthase deficiency","OBSOLETE: CMO I","OBSOLETE: CMO II","OBSOLETE: Corticosterone methyloxidase deficiency type I","OBSOLETE: FHHA1"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial hypoaldosteronism","url":"https://raremap.alftech.space/d/ORPHA-99763/","orphanet_url":"https://www.orpha.net/en/disease/detail/99763","names":{"fr":{"name":"OBSOLETE : Hypoaldostéronisme hyperréninémique familial type 1","synonyms":["OBSOLETE : Déficit en 18-oxydase","OBSOLETE : Déficit en aldostérone synthase","OBSOLETE : Déficit en corticostérone méthyloxydase type I","OBSOLETE : CMO I","OBSOLETE : CMO II","OBSOLETE : Déficit en 18-hydroxylase"]},"de":{"name":"OBSOLET: Hypoaldosteronismus, familiärer hyperreninämischer, Typ 1","synonyms":["OBSOLET: 18-Hydroxylase-Mangel","OBSOLET: 18-Oxydase-Mangel","OBSOLET: Aldosteron-Synthetase-Mangel","OBSOLET: CMO I","OBSOLET: CMO II","OBSOLET: Corticosteron-Methyloxidase-Mangel Typ I","OBSOLET: FHHA1"]},"es":{"name":"OBSOLETO: Hipoaldosteronismo hiperreninémico familiar tipo 1","synonyms":["OBSOLETO: CMO I","OBSOLETO: CMO II","OBSOLETO: Deficiencia de 18 hidroxilasa","OBSOLETO: Deficiencia de 18 oxidasa","OBSOLETO: Deficiencia de aldosterona sintasa","OBSOLETO: Deficiencia de corticosterona metil oxidasa tipo 1","OBSOLETO: FHHA1"]},"it":{"name":"OBSOLETO: Ipoaldosteronismo iperreninemico familiare, tipo 1","synonyms":["OBSOLETO: CMO I","OBSOLETO: CMO II","OBSOLETO: CMO 1","OBSOLETO: CMO 2","OBSOLETO: Deficit di 18-idrossilasi","OBSOLETO: Deficit di 18-ossidasi","OBSOLETO: Deficit di aldosterone sintasi","OBSOLETO: Deficit di corticosterone metil-ossidasi, tipo 1","OBSOLETO: FHHA1"]},"nl":{"name":"OBSOLEET: Familiaal hyperreninemisch hypoaldosteronisme type 1","synonyms":["OBSOLEET: 18-hydroxylasedeficiëntie","OBSOLEET: 18-oxidasedeficiëntie","OBSOLEET: Aldosteronsynthasedeficiëntie","OBSOLEET: CMO I","OBSOLEET: CMO II","OBSOLEET: Corticosteron-methyloxidasedeficiëntie type I","OBSOLEET: FHHA1"]},"pt":{"name":"OBSOLETO: Hipoaldosteronismo hiperreninémico, tipo 1 (FHHA1), familiar"},"pl":{"name":"NIEAKTUALNE: Rodzinny hipoaldosteronizm hiperreninowy typu 1","synonyms":["NIEAKTUALNE: CMO I","NIEAKTUALNE: CMO II","NIEAKTUALNE: FHHA1","NIEAKTUALNE: Niedobór hydrolazy 18","NIEAKTUALNE: Niedobór metyloksydazy kortykosteronu typu 1","NIEAKTUALNE: Niedobór oksydazy 18","NIEAKTUALNE: Niedobór syntazy aldosteronu"]},"cs":{"name":"NEAKTUÁLNÍ: Familiární hyperreninemický hypoaldosteronismus, typ 1","synonyms":["NEAKTUÁLNÍ: Deficit 18-hydroxylázy","NEAKTUÁLNÍ: Deficit 18-oxidázy","NEAKTUÁLNÍ: Deficit aldosteron syntázy","NEAKTUÁLNÍ: CMO I","NEAKTUÁLNÍ: CMO II","NEAKTUÁLNÍ: Deficit kortikosteron methyloxidázy, typ I","NEAKTUÁLNÍ: FHHA1"]},"uk":{"name":"ЗАСТАРІЛО: Сімейний гіперренінемічний гіпоальдостеронізм, тип 1","synonyms":["ЗАСТАРІЛО: Дефіцит 18-гідроксилази","ЗАСТАРІЛО: Дефіцит 18-оксидази","ЗАСТАРІЛО: Дефіцит альдостеронової синтази","ЗАСТАРІЛО: CMO I","ЗАСТАРІЛО: CMO II","ЗАСТАРІЛО: Дефіцит кортикостерон-метилоксидази I типу","ЗАСТАРІЛО: FHHA1"]},"zh":{"name":"弃用：家族性高肾素醛固酮减少症1型","synonyms":["皮质酮甲氧基氧化酶缺乏症I型"]},"tr":{"name":"Eski adı: ailesel hiperreninemik hipoaldosteronizm tip 1","synonyms":["CMO I","FHHA1","CMO II","18-oksidaz eksikliği","18-hidroksilaz eksikliği","Aldosteron sentaz eksikliği","Kortikosteron metiloksidaz eksikliği tip I"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":427,"name":"Familial hypoaldosteronism"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}