{"orpha":139380,"name":"OBSOLETE: Recessive hereditary methemoglobinemia type 2","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: NADH-cytochrome b5reductase deficiency type 2","OBSOLETE: NADH-diaphorase deficiency type 2","OBSOLETE: Recessive congenital methemoglobinemia type 2"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Hereditary methemoglobinemia","url":"https://raremap.alftech.space/d/ORPHA-139380/","orphanet_url":"https://www.orpha.net/en/disease/detail/139380","names":{"fr":{"name":"OBSOLETE : Méthémoglobinémie héréditaire autosomique récessive type 2","synonyms":["OBSOLETE : Déficit en NADH-cytochrome b5réductase type II","OBSOLETE : Déficit en NADH-diaphorase type II","OBSOLETE : Méthémoglobinémie congénitale autosomique récessive type 2"]},"de":{"name":"OBSOLET: Methämoglobinämie, hereditäre, rezessive, Typ 2","synonyms":["OBSOLET: Methämoglobinämie, kongenitale, rezessive, Typ II","OBSOLET: NADH Cytochrom b5-Reduktase-Mangel Typ II","OBSOLET: NADH-Diaphorase-Mangel Typ II"]},"es":{"name":"OBSOLETO: Metahemoglobinemia hereditaria recesiva tipo 2","synonyms":["OBSOLETO: Deficiencia de NADH-citocromo-b5-reductasa tipo 2","OBSOLETO: Deficiencia de NADH-diaforasa","OBSOLETO: Metahemoglobinemia congénita recesiva tipo 2"]},"it":{"name":"OBSOLETO: Metemoglobinemia ereditaria recessiva tipo 2","synonyms":["OBSOLETO: Carenza di NADH-citocromo b5 reduttasi tipo 2","OBSOLETO: Carenza di NADH-diaforasi tipo 2","OBSOLETO: Metemoglobinemia congenita recessiva tipo 2"]},"nl":{"name":"OBSOLEET: Recessieve erfelijke methemoglobinemie type 2","synonyms":["OBSOLEET: NADH-cytochroom b5-reductasedeficiëntie type 2","OBSOLEET: NADH-diaforasedeficiëntie type 2","OBSOLEET: Recessieve congenitale methemoglobinemie type 2"]},"pt":{"name":"OBSOLETO: Metemoglobinemia tipo II, congénita, autossómica recessiva"},"pl":{"name":"NIEAKTUALNE: Recesywna dziedziczna methemoglobinemia typu 2","synonyms":["NIEAKTUALNE: Niedobór diaforazy NADH typu 2","NIEAKTUALNE: Niedobór reduktazy NADH cytochromu b5 typu 2","NIEAKTUALNE: Recesywna wrodzona methemoglobinemia typu 2"]},"cs":{"name":"NEAKTUÁLNÍ: Recesivní dědičná methemoglobinémie, typ II","synonyms":["NEAKTUÁLNÍ: Deficit NADH-cytochrom b5 reduktázy, typ II","NEAKTUÁLNÍ: Deficit NADH-diaforázy, typ II"]},"uk":{"name":"ЗАСТАРІЛО: Рецесивна спадкова метгемоглобінемія, тип 2","synonyms":["ЗАСТАРІЛО: Дефіцит НАДН-цитохрому b5-редуктази типу 2","ЗАСТАРІЛО: Дефіцит NADH-діафорази 2 типу","ЗАСТАРІЛО: Рецесивна вроджена метгемоглобінемія типу 2"]},"zh":{"name":"弃用：隐性遗传高铁血红蛋白血症2型","synonyms":["隐性先天性高铁血红蛋白血症2型"]},"tr":{"name":"Eski adı: Resesif kalıtsal methemoglobinemi tip 2","synonyms":["NADH-diyaforaz eksikliği tip 2","NADH-sitokrom b5 redüktaz eksikliği tip 2","Çekinik doğumsal methemoglobinemia tip 2"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":621,"name":"Autosomal recessive methemoglobinemia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}