ORPHA:2706
OBSOLETE: Oculocerebroacral syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Oculocerebroacral syndrome | |
| fr | OBSOLETE : Syndrome oculo-cérébro-acral | |
| de | OBSOLET: Okulo-zerebro-akrales Syndrom | |
| es | OBSOLETO: Síndrome óculo-cerebro-acral | |
| it | OBSOLETO: Sindrome oculo-cerebro-acrale | |
| nl | OBSOLEET: Oculo-cerebro-acraal syndroom | |
| pt | OBSOLETO: Síndrome oculo-cerebro-acral | |
| pl | NIEAKTUALNE: Zespól oczno-mózgowo-konczynowy | |
| cs | NEAKTUÁLNÍ: Okulocerebroakrální syndrom | |
| uk | ЗАСТАРІЛО: Окулоцереброакральний синдром | |
| zh | 弃用：眼脑肢端综合征 | |
| tr | Eski adı: Oküloserebroakral sendrom |
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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/2706
- This record as JSON: /data/d/2706.json