FOXC1-related anterior segment dysgenesis
MONDO:0100235Mondo
Findings
No curated finding names FOXC1-related anterior segment dysgenesis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any anterior segment dysgenesis in which the cause of the disease is a mutation in the FOXC1 gene.
Definition from the Mondo Disease Ontology (MONDO:0100235), 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.
- FOXC1HGNC:3800
- Definitive · ClinGen · Autosomal dominant · 2021
Where it sits
- A kind of
- Narrower terms (2)