Term Name: | autosomal dominant keratitis |
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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 ) |