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General Information
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| Term |
posterior polymorphous corneal dystrophy 1 |
ID (Ontology) |
DOID:0110855 (Human Disease) |
| Definition |
A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. |
| Also Known As |
"CHED1" ; "Corneal Endothelial Dystrophy 1, Autosomal Dominant" ; "Maumenee Corneal Dystrophy" (for all, see Synonyms field below) |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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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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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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posterior polymorphous corneal dystrophy 1 | 1 | for disease ribbon | posterior polymorphous corneal dystrophy 1 | 1 | model of | posterior polymorphous corneal dystrophy 1 | 1 |
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Relationships