Term Name: autosomal dominant keratitis
Synonyms: hereditary keratitis
Definition: A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13.
Ontology: Human Disease [DOID:0111383]   ( DOID:0111383 )

Relationships
is a type of: autosomal dominant disease keratitis