raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1535

Craniosynostosis-dysmorphism-brachydactyly syndrome

inactive · moved to ORPHA:53271Muenke syndrome

Synonyms: Glass-Chapman-Hockley 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 Muenke syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCraniosynostosis-dysmorphism-brachydactyly syndromeGlass-Chapman-Hockley syndrome
frSyndrome de craniosynostose-brachydactylieSyndrome de Glass-Chapman-Hockley
deKraniosynostose-Dysmorphie-Brachydaktylie-SyndromGlass-Chapman-Hockley-Syndrom
esSíndrome de craneosinostosis-dismorfia-braquidactiliaSíndrome de Glass-Chapman-Hockley
itCraniosinostosi - brachidattiliaSindrome di Glass-Chapman-Hockley
nlCraniosynostose - dysmorfie - brachydactylie-syndroomSyndroom van Glass-Chapman-Hockley
ptSíndrome de craniossinostose-dismorfia-braquidactiliaSíndrome Glass-Chapman-Hockley
plKraniosynostoza - dysmorfizm - brachydaktyliaZespół Glassa, Chapmana i Hockley'a
csSyndrom zahrnující kraniosynostózu, dysmorfismus a brachydaktyliiGlassův-Chapmanův-Hockleyův syndrom · Glass-Chapman-Hockleyův syndrom
ukСиндром краніосиностозу-дизморфізму-брахідактиліїСиндром Гласса-Чепмена-Хоклі
zh颅缝早闭-外貌畸形-短指综合征Glass-Chapman-Hockley综合征
trKraniosinostozis-dismorfizm-brakidaktili sendromuGlass-Chapman-Hockley sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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