ORPHA:98677
OBSOLETE: Autosomal recessive syndromic optic atrophy
inactive · referred to ORPHA:441434Syndromic hereditary optic neuropathy
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Syndromic hereditary optic neuropathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal recessive syndromic optic atrophy | |
| fr | OBSOLETE : Atrophie optique syndromique autosomique récessive | |
| de | OBSOLET: Optikusatrophie, autosomal-rezessive, syndromale | |
| es | OBSOLETO: Atrofia óptica sindrómica autosómica recesiva | |
| it | OBSOLETO: Atrofia ottica sindromica, autosomica recessiva | |
| nl | OBSOLEET: Autosomaal recessieve syndromale optische atrofie | |
| pt | OBSOLETO: Atrofia óptica sindromática autossómica recessiva | |
| pl | NIEAKTUALNE: Autosomalny recesywny syndromiczny zanik nerwu wzrokowego | |
| cs | NEAKTUÁLNÍ: Autozomálně recesivní syndromická atrofie zrakového nervu | |
| uk | ЗАСТАРІЛО: Аутосомно-рецесивна синдромна атрофія зорового нерва | |
| zh | 弃用：常染色体隐性遗传视神经萎缩综合征 | |
| tr | Eski adı: Otozomal resesif sendromik optik atrofi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98677
- This record as JSON: /data/d/98677.json