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| Term | Edwards syndrome | ID (Ontology) | DOID:1085 (Human Disease) |
| Definition | A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18. | ||
| Also Known As | "Complete trisomy 18 syndrome" ; "E3 Trisomy" ; "trisomy 18" | ||
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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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chromosomal disease |__chromosomal duplication syndrome |__Edwards syndrome |
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| Is a | chromosomal duplication syndrome | ||
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ICD9CM:758.2 MESH:D000073842 NCI:C101362 SNOMEDCT_US_2023_03_01:51500006 UMLS_CUI:C0152096 |
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