corneal dystrophy, Meesmann, 2
MONDO:0032904Mondo
Findings
No curated finding names corneal dystrophy, Meesmann, 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- EpiphoraHPOHP:0009926
- PhotophobiaHPOHP:0000613
- Recurrent corneal erosionsHPOHP:0000495
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.
- KRT3HGNC:6440
- Strong · G2P · Autosomal dominant · 2017
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of