raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:620096

Non-syndromic unisutural craniosynostosis

Synonyms: Isolated unisutural craniosynostosis · Non-syndromic single suture synostosis

Type
Clinical group
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

10 of 12 languages
LangNameSynonyms
enNon-syndromic unisutural craniosynostosisIsolated unisutural craniosynostosis · Non-syndromic single suture synostosis
frCraniosynostose unisuturaire non syndromiqueCraniosynostose unisuturaire isolée
deKraniosynostose, unisuturale, nicht-syndromaleIsolierte monosuturale Kraniosynostose · Isolierte unisuturale Kraniosynostose
esCraneosinostosis unisutural no sindrómicaCraneosinostosis unisutural aislada · Sinostosis de sutura única no sindrómica
itCraniosinostosi monosuturale non sindromicaCraniosinostosi monosuturale isolata · Sinostosi di una sola sutura non sindromica
nlNiet-syndromale unisuturale craniosynostoseGeïsoleerde unisuturale craniosynostose · Niet-syndromale synostose van een enkele schedelnaad
ptCraniossinostose unisutural não-sindromáticaCraniossinostose unisutural isolada · Sinostose de sutura única não-sindromática
plNiesyndromiczna kraniosynostoza obejmująca jeden szew= en
csNesyndromická unisuturální kraniosynostóza= en
ukНесиндромальний унісутуральний краніосиностозІзольований однобічний краніосиностоз · Несиндромний синостоз одного шва
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0850072Evalidated
UMLSC5680403Evalidated

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 (6):

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