OBO ID: DOID:0060673 |
Term Name: | Peters anomaly | Search Ontology: | |
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Definition: | A corneal disease characterized by a central corneal leukoma and absence of the posterior corneal stroma and Descemet membrane that has_material_basis_in mutation in the PAX6 gene on chromosome 11p13, the PITX2 gene on chromosome 4q25, the CYP1B1 gene on chromosome 2p22.2, or the FOXC1 gene on chromosome 6p25.3. (3) | ||
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Ontology: | Human Disease ( DOID:0060673 ) |
OTHER Peters anomaly PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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