ORPHA:669
OBSOLETE: Otopalatodigital syndrome
inactive · referred to ORPHA:364541Otopalatodigital syndrome spectrum disorder
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Otopalatodigital syndrome spectrum disorder
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Otopalatodigital syndrome | |
| fr | OBSOLETE : Syndrome oto-palato-digital | |
| de | OBSOLET: Oto-palato-digitales Syndrom | |
| es | OBSOLETO: Síndrome oto-palato-digital | |
| it | OBSOLETO: Sindrome oto-palato-digitale | OBSOLETO: Sindrome di Taybi |
| nl | OBSOLEET: Otopalatodigitaal syndroom | |
| pt | OBSOLETO: Síndrome oto-palato-digital | OBSOLETO: OPD · OBSOLETO: Síndrome Taybi |
| pl | NIEAKTUALNE: Zespól uszno-podniebienno-palcowy | NIEAKTUALNE: Zespół Taybiego |
| cs | NEAKTUÁLNÍ: Otopalatodigitální syndrom | NEAKTUÁLNÍ: Taybiho syndrom |
| uk | ЗАСТАРІЛО: Отопалатодігітальний синдром | |
| zh | 弃用：耳腭指综合征 | |
| tr | Eski adı: Otopalatodijital sendromu |
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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/669
- This record as JSON: /data/d/669.json