raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93451

Cleidocranial dysplasia and isolated cranial ossification defect

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCleidocranial dysplasia and isolated cranial ossification defect
frDysplasie cleido-crânienne et défaut d'ossification du crâne isolé
deKleidokraniale Dysplasie und isolierten kranialen Ossifikationsdefekt
esDisplasia cleidocraneal y defecto de osificación craneal aislado
itDisplasia cleidocranica e difetto isolato dell'ossificazione del cranio
nlCleidocraniale dysplasie en geïsoleerd craniale ossificatiedefect
ptDisplasia cleidocraniana e defeito de ossificação craniana isolado
plGrupa dysplazji obojczykowo-czaszkowych
csKleidokraniální dysplázie a izolované defekty kraniální osifikace
ukКлідокраніальна дисплазія та ізольований дефект окостеніння черепа
zh锁骨颅骨发育不良伴孤立型颅骨骨化缺陷
trKleidokraniyal displazi ve izole kraniyal ossifikasyon defekti
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681593Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (2):

Children (6):

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