ORPHA:139373
OBSOLETE: Recessive hereditary methemoglobinemia type 1
inactive · referred to ORPHA:621Autosomal recessive methemoglobinemia
Synonyms: OBSOLETE: NADH-cytochrome b5reductase deficiency type 1 · OBSOLETE: NADH-diaphorase deficiency type 1 · OBSOLETE: Recessive congenital methemoglobinemia type 1
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Hereditary methemoglobinemia
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Recessive hereditary methemoglobinemia type 1 | OBSOLETE: NADH-cytochrome b5reductase deficiency type 1 · OBSOLETE: NADH-diaphorase deficiency type 1 · OBSOLETE: Recessive congenital methemoglobinemia type 1 |
| fr | OBSOLETE : Méthémoglobinémie héréditaire autosomique récessive type 1 | OBSOLETE : Déficit congénital en NADH-cytochrome b5 réductase type I · OBSOLETE : Déficit en NADH-diaphorase type I · OBSOLETE : Déficit en ferrihémoglobine-réductase · OBSOLETE : Méthémoglobinémie congénitale autosomique récessive type 1 |
| de | OBSOLET: Methämoglobinämie, hereditäre, rezessive, Typ 1 | OBSOLET: Methämoglobinämie, kongenitale, rezessive, Typ I · OBSOLET: NADH Cytochrom b5-Reduktase-Mangel Typ I · OBSOLET: NADH-Diaphorase-Mangel Typ I |
| es | OBSOLETO: Metahemoglobinemia hereditaria recesiva tipo 1 | OBSOLETO: Metahemoglobinemia congénita recesiva tipo 1 · OBSOLETO: Deficiencia de NADH-citocromo-b5-reductasa tipo 1 · OBSOLETO: Deficiencia de NADH-diaforasa tipo 1 |
| it | OBSOLETO: Metemoglobinemia ereditaria recessiva tipo 1 | OBSOLETO: Deficit di NADH-citocromo b5 reduttasi · OBSOLETO: Deficit di NADH-diaforasi tipo 1 · OBSOLETO: Metaemoglobinemia congenita recessiva tipo 1 |
| nl | OBSOLEET: Recessieve erfelijke methemoglobinemie type 1 | OBSOLEET: NADH-cytochroom b5-reductasedeficiëntie type 1 · OBSOLEET: NADH-diaforasedeficiëntie type 1 · OBSOLEET: Recessieve congenitale methemoglobinemie type 1 |
| pt | OBSOLETO: Metemoglobinemia tipo I, congénita, autossómica recessiva | |
| pl | NIEAKTUALNE: Recesywna dziedziczna methemoglobinemia typu 1 | NIEAKTUALNE: Niedobór diaforazy NADH typu 1 · NIEAKTUALNE: Niedobór reduktazy NADH cytochromu b5 typu 1 · NIEAKTUALNE: Recesywna wrodzona methemoglobinemia typu 1 |
| cs | NEAKTUÁLNÍ: Recesivní dědičná methemoglobinémie, typ I | NEAKTUÁLNÍ: Deficit NADH-cytochrom b5 reduktázy, typ I · NEAKTUÁLNÍ: Deficit NADH-diaforázy, typ I |
| uk | ЗАСТАРІЛО: Рецесивна спадкова метгемоглобінемія, тип 1 | ЗАСТАРІЛО: Дефіцит НАДН-цитохрому b5-редуктази типу 1 · ЗАСТАРІЛО: Дефіцит NADH-діафорази типу 1 · ЗАСТАРІЛО: Рецесивна вроджена метгемоглобінемія типу 1 |
| zh | 弃用：隐性遗传高铁血红蛋白血症1型 | 隐性先天性高铁血红蛋白血症1型 |
| tr | Eski adı: Resesif kalıtsal methemoglobinemi tip 1 | NADH-diyaforaz eksikliği tip 1 · NADH-sitokrom b5 redüktaz eksikliği tip 1 · Çekinik doğumsal methemoglobinemia tip 1 |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/139373
- This record as JSON: /data/d/139373.json