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| Term | posterior amorphous corneal dystrophy | ID (Ontology) | DOID:0060452 (Human Disease) |
| Definition | A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome. | ||
| Also Known As | "chromosome 12q21.33 deletion syndrome" ; "PACD" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease_____ chromosomal disease | |__chromosomal deletion syndrome__| corneal dystrophy | |__stromal dystrophy______________| posterior amorphous corneal dystrophy |
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| Is a |
autosomal dominant disease chromosomal deletion syndrome stromal dystrophy |
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ICD10CM:H18.5 MESH:C567546 MIM:612868 ORDO:98971 |
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