ORPHA:3423
Vasquez-Hurst-Sotos syndrome
inactive · moved to ORPHA:261483Xq27.3q28 duplication syndrome
Synonyms: Hypogonadism-gynecomastia-X-linked intellectual disability 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 Xq27.3q28 duplication syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Vasquez-Hurst-Sotos syndrome | Hypogonadism-gynecomastia-X-linked intellectual disability syndrome |
| fr | Syndrome de Vasquez-Hurst-Sotos | Syndrome d'hypogonadisme-gynécomastie-déficience intellectuelle lié à l'X |
| de | Vasquez-Hurst-Sotos-Syndrom | |
| es | Síndrome de Vasquez-Hurst-Sotos | Síndrome de hipogonadismo-ginecomastia-discapacidad intelectual ligada al cromosoma X |
| it | Sindrome di Vasquez-Hurst-Sotos | Sindrome ipogonadismo legato all'X-ginecomastia-disabilità intellettiva |
| nl | Syndroom van Vasquez-Hurst-Sotos | Hypogonadisme - gynaecomastie - X-gebonden intellectuele achterstand-syndroom |
| pt | Síndrome Vasquez-Hurst-Sotos | Síndrome de hipogonadismo-ginecomastia-perturbação do desenvolvimento intelectual ligada ao X |
| pl | Zespół Vasqueza, Hursta i Sotosa | Hipogonadyzm - ginekomastia - niepełnosprawnoś intelektualna sprzężona z chromosomem X |
| cs | Vasquezův-Hurstův-Sotosův syndrom | Syndrom zahrnující hypogonadismus, gynekomastii a X-vázanou mentální retardaci · Vasquez-Hurst-Sotosův syndrom |
| uk | Синдром Васкез-Херста-Сотоса | Х-зчеплений синдром гіпогонадизму-гінекомастії- інтелектуальної недостатності |
| zh | Vasquez-Hurst-Sotos综合征 | 性腺功能减退症-男子乳腺发育-X连锁智力障碍综合征 |
| tr | Vasquez-Hurst-Sotos sendromu | Hipogonadizm-jinekomasti-X'e bağlı zihinsel yetersizlik sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C536533 | E | validated | |
| UMLS | C2931231 | 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/3423
- This record as JSON: /data/d/3423.json