ORPHA:1557
Cutis verticis gyrata-intellectual disability syndrome
inactive · moved to ORPHA:357225Primary non-essential cutis verticis gyrata
Synonyms: McDowall 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 Primary non-essential cutis verticis gyrata
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cutis verticis gyrata-intellectual disability syndrome | McDowall syndrome |
| fr | Syndrome de cutis verticis gyrata-déficience intellectuelle | Syndrome de McDowall |
| de | Cutis verticis gyrata-Intelligenzminderung-Syndrom | McDowall-Syndrom |
| es | Síndrome de cutis verticis gyrata-discapacidad intelectual | Síndrome de McDowall |
| it | Sindrome da cutis verticis gyrata-disabilità intellettiva | Sindrome di McDowall |
| nl | Cutis verticis gyrata - intellectuele achterstand-syndroom | Syndroom van McDowall |
| pt | Síndrome de cutis verticis gyrata-perturbação do desenvolvimento intelectual | Síndrome McDowall |
| pl | Skóra kręta ciemienia - niepełnosprawność intelektualna | Zespół McDowalla |
| cs | Syndrom zahrnující cutis verticis gyrata a mentální retardaci | McDowallův syndrom |
| uk | Синдром складчастої пахідермії-інтелектуальної недостатності | Синдром Макдауелла |
| zh | 回状颅皮-智力障碍综合征 | McDowall综合征 |
| tr | Cutis verticis gyrata-zihinsel yetersizlik sendromu | McDowall 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/1557
- This record as JSON: /data/d/1557.json