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| Term | epithelial basement membrane dystrophy | ID (Ontology) | DOID:0060447 (Human Disease) |
| Definition | An epithelial and subepithelial dystrophy that is characterized by sheet-like areas of basement membrane originating from the basal epithelial cells of the corneal epithelium and extending superficially into the epithelium. | ||
| Also Known As | "Cogan corneal dystrophy" ; "EBMD" ; "microcystic corneal dystrophy" | ||
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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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autosomal genetic disease |__autosomal dominant disease______________ corneal dystrophy | |__epithelial and subepithelial dystrophy__| epithelial basement membrane dystrophy 3 rec. |
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Relationships
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| Is a |
autosomal dominant disease epithelial and subepithelial dystrophy |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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ICD10CM:H18.5 MESH:C535477 MIM:121820 ORDO:98956 |
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