Term Name: Meesmann corneal dystrophy 1
Synonyms:
Definition: A Messmann corneal dystrophy that is characterized by the presence of multitudinous microcysts within the anterior epithelium and that has_material_basis_in heterozygous mutation in the KRT12 gene on chromosome 17q21.
Ontology: Human Disease [DOID:0080670]   ( DOID:0080670 )

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