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| Term | chromosome 9p deletion syndrome | ID (Ontology) | DOID:0060732 (Human Disease) |
| Definition | A chromosomal deletion syndrome characterized by trigonocephaly, flattened occiput midface hypoplasia, long philtrum, prominent forehead, broad flat nasal bridge, anteverted nares, malformed external ears, hypertelorism, hypertonia, delayed psychomotor development and that has_material_basis_in a contiguous gene deletion on the short arm of chromosome 9. | ||
| Also Known As | "9p syndrome" ; "Alfi syndrome" ; "monosomy 9p syndrome" | ||
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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 deletion syndrome |__chromosome 9p deletion syndrome |
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| Is a | chromosomal deletion syndrome | ||
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ICD10CM:Q93.5 MESH:C538024 MIM:158170 ORDO:261112 |
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