raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93452

OBSOLETE: Craniosynostosis syndrome or cranial ossification disease

inactive · referred to ORPHA:139393Syndromic craniosynostosis

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Syndromic craniosynostosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Craniosynostosis syndrome or cranial ossification disease
frOBSOLETE : Craniosténose ou anomalie de l'ossification crânienne
deOBSOLET: Kraniosynostose-Syndrom und kraniale Verknöcherung
esOBSOLETO: Síndrome de craneosinostosis o enfermedad de la osificación craneal
itOBSOLETO: Sindrome da craniosinostosi e malattia dell'ossificazione cranica
nlOBSOLEET: Craniosynostosesyndroom van craniale ossificatieziekte
ptOBSOLETO: Síndrome craniossinostose e doença da ossificação craniana
plNIEAKTUALNE: Zespól kraniosynostozy lub zaburzenia kostnienia czaszki
csNEAKTUÁLNÍ: Syndrom kraniosynostózy nebo onemocnění osifikace lebky
ukЗАСТАРІЛО: Синдром краніосиностозу або хвороба окостеніння черепа
zh弃用:颅缝早闭综合征或颅缝骨化症
trEski adı: Kraniosinostozis sendromu veya kraniyal ossifikasyon hastalığı
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