ORPHA:441344
OBSOLETE: Autosomal recessive optic atrophy, OPA9 type
inactive · referred to ORPHA:98676Autosomal recessive isolated optic atrophy
- 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 Autosomal recessive isolated optic atrophy
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal recessive optic atrophy, OPA9 type | |
| fr | OBSOLETE : Atrophie optique autosomique récessive type OPA9 | |
| de | OBSOLET: Optikusatrophie, autosomal-rezessive, Typ OPA9 | |
| es | OBSOLETO: Atrofia óptica autosómica recesiva tipo OPA9 | |
| it | OBSOLETO: Atrofia ottica autosomica recessiva, tipo OPA8 | |
| nl | OBSOLEET: Autosomaal recessieve opticusatrofie, type OPA9 | |
| pt | OBSOLETO: Atrofia óptica autossómica recessiva, tipo OPA9 | |
| pl | NIEAKTUALNE: Autosomalny recesywny zanik nerwu wzrokowego, typ OPA9 | |
| cs | NEAKTUÁLNÍ: Autozomálně recesivní optická atrofie, OPA8 typ | |
| uk | ЗАСТАРІЛО: Аутосомно-рецесивна атрофія зорового нерва, тип OPA9 | |
| zh | 弃用：常染色体隐性遗传性视神经萎缩，OPA9型 | |
| tr | Eski adı: Otozomal resesif optik atrofi, OPA9 tipi |
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/441344
- This record as JSON: /data/d/441344.json