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| Term | autosomal dominant intellectual developmental disorder 22 | ID (Ontology) | DOID:0070052 (Human Disease) |
| Definition | An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZBTB18 gene on chromosome 1q44. | ||
| Also Known As | "autosomal dominant mental retardation 22" ; "autosomal dominant non-syndromic intellectual disability 22" ; "MRD22" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal dominant disease__ intellectual disability_____| autosomal dominant intellectual developmental disorder |__autosomal dominant intellectual developmental disorder 22 |
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| Is a | autosomal dominant intellectual developmental disorder | ||
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| MIM:612337 | |||