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A reference for what the literature reports. Not medical advice.

Disease

GRHL3-related orofacial clefting

MONDO:0100579Mondo

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Findings

No curated finding names GRHL3-related orofacial clefting yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any orofacial clefting in which the cause of the disease is a mutation in the GRHL3 gene.

Definition from the Mondo Disease Ontology (MONDO:0100579), read 2026-09-29. CC BY 4.0.

Genes

1 gene

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

GRHL3HGNC:25839
- Definitive · ClinGen · Autosomal dominant · 2024

Where it sits

A kind of: orofacial cleft