Term Name: Meesmann corneal dystrophy 2
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.
Ontology: Human Disease [DOID:0080671]   ( DOID:0080671 )

Relationships
is a type of: autosomal dominant disease Meesmann corneal dystrophy