Cleft palate

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Cleft palate

ORPHA:2014Clinical group

What it is

A fissure type embryopathy that affects the soft and hard palate to varying degrees.

Key facts

Prevalence
1-5 / 10 000 (Europe)
Age of onset
Antenatal, Neonatal
Inheritance
Multigenic/multifactorial, Not applicable
Classified as
Clinical group

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Genes reported in subtypes

GRHL3UBB

Orphanet records these genes on 4 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

ICD-10 codes

Q35ICD-10 names this disease exactly

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 1896MEDDRA 10009269MESH D002972MONDO 0016064MONDO 16064OMIM 119540UMLS C0008925

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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