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| Term | chromosome Xp11.23-p11.22 duplication syndrome | ID (Ontology) | DOID:0060461 (Human Disease) |
| Definition | A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome Xp11.23-p11.22 region. | ||
| Also Known As | "microduplication Xp11.22-p11.23 syndrome" ; "trisomy Xp11.22-p11.23" | ||
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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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X-linked monogenic disease |__X-linked dominant disease_________ chromosomal disease | |__chromosomal duplication syndrome__| chromosome Xp11.23-p11.22 duplication syndrome |
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| Is a |
chromosomal duplication syndrome X-linked dominant disease |
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External Crossreferences & Linkouts
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ICD10CM:Q99.8 MESH:C567585 MIM:300801 ORDO:217377 |
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