ORPHA:3349
Treft-Sanborn-Carey syndrome
inactive · moved to ORPHA:1215Autosomal dominant optic atrophy plus syndrome
Synonyms: Optic atrophy-ophthalmoplegia-ptosis-deafness-myopathy syndrome · Optic atrophy-ophthalmoplegia-ptosis-hearing loss-myopathy syndrome
- 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 optic atrophy plus syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Treft-Sanborn-Carey syndrome | Optic atrophy-ophthalmoplegia-ptosis-deafness-myopathy syndrome · Optic atrophy-ophthalmoplegia-ptosis-hearing loss-myopathy syndrome |
| fr | Syndrome de Treft-Sanborn-Carey | Syndrome d'atrophie optique-ophtalmoplégie-ptosis-surdité-myopathie |
| de | Treft-Sanborn-Carey-Syndrom | Optikusatrophie - Ptosis - Ophthalmoplegie - Myopathie - Taubheit |
| es | Síndrome de Treft-Sanborn-Carey | Síndrome de atrofia óptica-oftalmoplejía-ptosis-hipoacusia-miopatía · Síndrome de atrofia óptica-oftalmoplejía-ptosis-sordera-miopatía |
| it | Sindrome di Treft-Sanborn-Carey | Atrofia ottica - oftalmoplegia - ptosi - sordità - miopatia |
| nl | Syndroom van Treft-Sanborn-Carey | Opticusatrofie - oftalmoplegie - ptose - doofheid - myopathie-syndroom |
| pt | Síndrome Treft-Sanborn-Carey | Síndrome de atrofia óptica-oftalmoplegia-ptose-perda auditiva-miopatia · Síndrome de atrofia óptica-oftalmoplegia-ptose-surdez-miopatia |
| pl | Zespół Trefta, Sanborna i Careya | Atrofia nerwu wzrokowego- oftalmoplegia- ptoza - głuchota - miopatia |
| cs | Treftův-Sanbornův-Careyův syndrom | Syndrom zahrnující atrofii optického nervu, oftalmoplegii, ptózu, hluchotu a myopatii · Treft-Sanborn-Careyův syndrom |
| uk | Синдром Трефта-Санборна-Кейрі | Синдром атрофії зорового нерва - офтальмоплегія - птоз - глухота - міопатія · Синдром атрофії зорового нерва - офтальмоплегія - птоз - втрати слуху - міопатія |
| zh | Treft-Sanborn-Carey综合征 | 视神经萎缩-眼肌麻痹-上睑下垂-听觉丧失-肌病综合征 |
| tr | Treft-Sanborn-Carey sendromu | Optik atrofi-oftalmopleji-ptozis-sağırlık-miyopati sendromu · Optik atrofi-oftalmopleji-ptoz-işitme kaybı-miyopati sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C536544 | E | validated | |
| UMLS | C2931235 | 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/3349
- This record as JSON: /data/d/3349.json