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| Term | steatocystoma multiplex | ID (Ontology) | DOID:0111556 (Human Disease) |
| Definition | A sebaceous gland disease characterized by the presence of multiple benign sebaceous cysts that has_material_basis_in heterozygous mutation in the KRT17 gene on chromosome 17q21.2. | ||
| Also Known As | "multiple sebaceous cysts" ; "sebocystomatosis" | ||
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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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autosomal genetic disease |__autosomal dominant disease__ skin disease | |__sebaceous gland disease_____| steatocystoma multiplex |
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| Is a |
autosomal dominant disease sebaceous gland disease |
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External Crossreferences & Linkouts
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GARD:5003 MESH:D062685 MIM:184500 ORDO:841 |
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