Search Ontology:
Human Disease

Meesmann corneal dystrophy 2

Term ID
DOID:0080671
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models