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General Information
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| Term |
autosomal dominant intellectual developmental disorder 61 |
ID (Ontology) |
DOID:0061034 (Human Disease) |
| Definition |
An autosomal dominant intellectual developmental disorder characterized by global developmental delay apparent in infancy with mildly impaired intellectual development, expressive speech delay, and behavioral abnormalities, including autism spectrum disorder and attention deficit-hyperactivity disorder (ADHD) that has_material_basis_in heterozygous mutation in the MED13 gene on chromosome 17q23. |
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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 61 | 1 | for disease ribbon | autosomal dominant intellectual developmental disorder 61 | 1 | model of | autosomal dominant intellectual developmental disorder 61 | 1 |
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