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| Term | posterior polymorphous corneal dystrophy 2 | ID (Ontology) | DOID:0110856 (Human Disease) |
| Definition | A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the COL8A2 gene on chromosome 1p34.3. | ||
| Also Known As | "PPCD2" | ||
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autosomal genetic disease |__autosomal dominant disease________________ corneal dystrophy | |__posterior polymorphous corneal dystrophy__| posterior polymorphous corneal dystrophy 2 |
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| Is a |
autosomal dominant disease posterior polymorphous corneal dystrophy |
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ICD10CM:H18.50 MIM:609140 |
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