raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:139390

Non-syndromic craniosynostosis

Synonyms: Isolated craniosynostosis

Type
Clinical group
Group
Group of disorders
Age of onset
Infancy, Neonatal
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
enNon-syndromic craniosynostosisIsolated craniosynostosis
frCraniosynostose non syndromiqueCraniosynostose isolée
deKraniosynostose, nicht-syndromaleIsolierte Kraniosynostose
esCraneosinostosis no sindrómicaCraneosinostosis aislada
itCraniosinostosi non sindromicaCraniosinostosi isolata
nlNiet-syndromale craniosynostoseGeïsoleerde craniosynostose
ptCraniossinostose não-sindromáticaCraniossinostose isolada
plKraniosynostoza izolowanaNiesyndromiczna kraniosynostoza
csIzolovaná kraniosynostóza= en
ukНесиндромальний краніосиностозІзольований краніосиностоз
zh孤立性颅缝早闭
trİzole kraniyosinostoz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0015337Evalidated
MONDO15337Evalidated
UMLSC5848302Evalidated
GARD19910Evalidated

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 (1):

Children (2):

Codes that Orphanet moved or referred to this one:

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