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| Term | chromosome 19q13.11 deletion syndrome | ID (Ontology) | DOID:0060408 (Human Disease) |
| Definition | A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties. | ||
| Also Known As | "19q13.11 microdeletion syndrome" ; "monosomy 19q13.11" | ||
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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_____ chromosomal disease | |__chromosomal deletion syndrome__| chromosome 19q13.11 deletion syndrome |
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| Is a |
autosomal dominant disease chromosomal deletion syndrome |
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External Crossreferences & Linkouts
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GARD:10592 MESH:C567810 MIM:613026 ORDO:217346 UMLS_CUI:C2751651 |
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