corneal dystrophy, Fuchs endothelial, 3
MONDO:0013203Mondo
Findings
No curated finding names corneal dystrophy, Fuchs endothelial, 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Fuchs' endothelial dystrophy in which the cause of the disease is a mutation in the TCF4 gene.
Definition from the Mondo Disease Ontology (MONDO:0013203), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
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.
- TCF4HGNC:11634
- Strong · G2P · Autosomal dominant · 2017
Where it sits
- A kind of
Other names
3 names
Resolves to: corneal dystrophy, Fuchs endothelial, 3
- Also called
- corneal dystrophy, Fuchs endothelial, type 3Fuchs' endothelial dystrophy caused by mutation in TCF4TCF4 Fuchs' endothelial dystrophy