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| Term | posterior polymorphous corneal dystrophy 3 | ID (Ontology) | DOID:0110857 (Human Disease) |
| Definition | A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the ZEB1 gene on chromosome 10p11.22. | ||
| Also Known As | "PPCD3" | ||
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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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corneal dystrophy |__posterior polymorphous corneal dystrophy__ genetic disease | |__monogenic disease_________________________| posterior polymorphous corneal dystrophy 3 1 rec. |
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| Is a |
monogenic disease posterior polymorphous corneal dystrophy |
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External Crossreferences & Linkouts
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ICD10CM:H18.50 MIM:609141 |
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