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| Term | syndromic X-linked intellectual disability 12 | ID (Ontology) | DOID:0060804 (Human Disease) |
| Definition | A syndromic X-linked intellectual disability characterized by severe intellectual deficit, mutism, epilepsy, growth retardation or failure and recurrent infections that has_material_basis_in variation in the chromosome region Xp11. | ||
| Also Known As | "mental retardation, X-linked, syndromic 12" ; "X-linked intellectual disability, Wilson type" | ||
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| DO.org | |||
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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_________ syndromic intellectual disability__| syndromic X-linked intellectual disability |__syndromic X-linked intellectual disability 12 |
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| Is a | syndromic X-linked intellectual disability | ||
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ICD10CM:Q87.8 MIM:309545 ORDO:85290 |
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