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General Information
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| Term |
autosomal dominant intellectual developmental disorder 13 |
ID (Ontology) |
DOID:0070043 (Human Disease) |
| Definition |
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31. |
| Also Known As |
"autosomal dominant mental retardation 13" ; "autosomal dominant non-syndromic intellectual disability 13" ; "mental retardation, autosomal dominant 13, with neuronal migration defects" (for all, see Synonyms field below) |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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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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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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autosomal dominant intellectual developmental disorder 13 | 1 | for disease ribbon | autosomal dominant intellectual developmental disorder 13 | 1 | model of | autosomal dominant intellectual developmental disorder 13 | 1 |
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