ORPHA:77302
Oculo-oto-facial dysplasia
inactive · moved to ORPHA:1200Burn-McKeown syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Burn-McKeown syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Oculo-oto-facial dysplasia | |
| fr | Dysplasie oculo-oto-faciale | |
| de | Dysplasie, okulo-oto-faziale | |
| es | Displasia óculo-oto-facial | |
| it | Displasia oculo-oto-faciale | |
| nl | Oculo-oto-faciale dysplasie | |
| pt | Displasia oculo-oto-facial | |
| pl | Dysplazja oczno-uszno-twarzowa | |
| cs | Okulootofaciální dysplázie | Burnův-McKeownův syndrom · Burn-McKeownův syndrom |
| uk | Окулоотофаціальна дисплазія | |
| zh | 眼-耳-面发育不良 | |
| tr | Okülo-oto-yüz displazisi |
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/77302
- This record as JSON: /data/d/77302.json