ORPHA:1767
Familial progressive vestibulocochlear dysfunction
inactive · moved to ORPHA:90635Autosomal dominant non-syndromic genetic deafness
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant non-syndromic sensorineural deafness type DFNA
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial progressive vestibulocochlear dysfunction | |
| fr | Dysfonctionnement vestibulo-cochléaire progressif familial | |
| de | Vestibulocochleäre Dysfunktion, progressive, familiärer Typ | |
| es | Disfunción vestibulococlear progresiva familiar | |
| it | Disfunzione vestibolo-cocleare progressiva familiare | |
| nl | Familiale progressieve vestibulocochleaire disfunctie | |
| pt | Disfunção vestibulo-coclear progressiva familiar | |
| pl | Rodzinna postępująca dysfunkcja przedsionkowo-ślimakowa | |
| cs | Familiární progresivní vestibulokochleární dysfunkce | |
| uk | Сімейна прогресуюча вестибулокохлеарна дисфункція | |
| zh | 家族性进行性前庭耳蜗功能障碍 | |
| tr | Ailesel ilerleyici vestibülokoklear disfonksiyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 193005 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/1767
- This record as JSON: /data/d/1767.json