OBO ID: DOID:0111383 |
Term Name: | autosomal dominant keratitis | Search Ontology: | |
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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. https://www.ncbi.nlm.nih.gov/pubmed/7668281 | ||
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Ontology: | Human Disease ( DOID:0111383 ) |
OTHER autosomal dominant keratitis PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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