Search Ontology:
Human Disease
Meesmann corneal dystrophy 2
- Term ID
- DOID:0080671
- Synonyms
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- Definition
- A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13. https://pubmed.ncbi.nlm.nih.gov/18806880/
- References
- Ontology
- Human Disease ( DOID:0080671 )
- is a type of
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Genes Involved
Zebrafish Models