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| Term | Peters anomaly | ID (Ontology) | DOID:0060673 (Human Disease) |
| 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. | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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eye disease |__corneal disease |__Peters anomaly 2 rec. |
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| Is a | corneal disease | ||
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External Crossreferences & Linkouts
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GARD:7377 ICD10CM:Q13.4 MESH:C537884 MIM:604229 ORDO:708 |
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