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

Disease

ARHGAP29-related non-syndromic orofacial cleft

MONDO:1060132Mondo

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Findings

No curated finding names ARHGAP29-related non-syndromic orofacial cleft yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any orofacial cleft in which the cause of the disease is a mutation in the ARHGAP29 gene.

Definition from the Mondo Disease Ontology (MONDO:1060132), 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.

ARHGAP29HGNC:30207
- Definitive · ClinGen · Autosomal dominant · 2024

Where it sits

A kind of: orofacial cleft