ORPHA:352740
Ocular albinism with congenital sensorineural deafness
inactive · moved to ORPHA:895Waardenburg syndrome type 2
Synonyms: Ocular albinism with congenital sensorineural hearing loss · Waardenburg syndrome type 2 with ocular albinism
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Waardenburg syndrome type 2
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ocular albinism with congenital sensorineural deafness | Ocular albinism with congenital sensorineural hearing loss · Waardenburg syndrome type 2 with ocular albinism |
| fr | Albinisme oculaire avec surdité neurosensorielle congénitale | Syndrome de Waardenburg type 2 avec albinisme oculaire |
| de | Okulärer Albinismus mit kongenitaler sensorineuraler Schwerhörigkeit | Waardenburg-Syndrom Typ 2 mit okulärem Albinismus |
| es | Albinismo ocular con sordera neurosensorial congénita | Síndrome de Waardenburg con albinismo ocular · Albinismo ocular con hipoacusia neurosensorial congénita |
| it | Albinismo oculare con sordità neurosensoriale congenita | Sindrome di Waardenburg tipo 2 con albinismo oculare |
| nl | Oculair albinisme met congenitale sensorineurale doofheid | Oculair albinisme met congenitaal sensorineuraal gehoorverlies · Syndroom van Waardenburg type 2 met oculair albinisme |
| pt | Albinismo ocular com surdez neurossensorial congénita | |
| pl | Albinizm oczny z głuchotą zmysłowo-nerwową | Zespół Waardenburga typu 2 z albinizmem ocznym |
| cs | Okulární albinismus s vrozenou senzorineurální hluchotou | Waardenburgův syndrom, typ 2 s okulárním albinismem |
| uk | Очний альбінізм з вродженою сенсоневральною глухотою | Очний альбінізм з вродженою сенсоневральною приглухуватістю · Синдром Ваарденбурга типу 2 з очним альбінізмом |
| zh | 眼白化病伴先天性感音神经性聋 | 眼白化病班先天性感音听力丧失 |
| tr | Doğumsal sensörinöral sağırlık ile seyreden oküler albinizm | Oküler albinizm ile seyreden Waardenburg sendromu tip 2 · Doğumsal sensörinöral işitme kaybı ile seyreden oküler albinizm |
Definition in:
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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/352740
- This record as JSON: /data/d/352740.json