raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enVasquez-Hurst-Sotos syndromeHypogonadism-gynecomastia-X-linked intellectual disability syndrome
frSyndrome de Vasquez-Hurst-SotosSyndrome d'hypogonadisme-gynécomastie-déficience intellectuelle lié à l'X
deVasquez-Hurst-Sotos-Syndrom
esSíndrome de Vasquez-Hurst-SotosSíndrome de hipogonadismo-ginecomastia-discapacidad intelectual ligada al cromosoma X
itSindrome di Vasquez-Hurst-SotosSindrome ipogonadismo legato all'X-ginecomastia-disabilità intellettiva
nlSyndroom van Vasquez-Hurst-SotosHypogonadisme - gynaecomastie - X-gebonden intellectuele achterstand-syndroom
ptSíndrome Vasquez-Hurst-SotosSíndrome de hipogonadismo-ginecomastia-perturbação do desenvolvimento intelectual ligada ao X
plZespół Vasqueza, Hursta i SotosaHipogonadyzm - ginekomastia - niepełnosprawnoś intelektualna sprzężona z chromosomem X
csVasquezův-Hurstův-Sotosův syndromSyndrom zahrnující hypogonadismus, gynekomastii a X-vázanou mentální retardaci · Vasquez-Hurst-Sotosův syndrom
ukСиндром Васкез-Херста-СотосаХ-зчеплений синдром гіпогонадизму-гінекомастії- інтелектуальної недостатності
zhVasquez-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
trVasquez-Hurst-Sotos sendromuHipogonadizm-jinekomasti-X'e bağlı zihinsel yetersizlik sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MeSHC536533Evalidated
UMLSC2931231Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card