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General Information
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| Term |
autosomal dominant intellectual developmental disorder 72 |
ID (Ontology) |
DOID:0061045 (Human Disease) |
| Definition |
An autosomal dominant intellectual developmental disorder characterized by developmental delay, predominant speech delay, autistic or attention-deficit/hyperactivity disorder features, overfriendliness, generalized hypotonia, overweight/obesity, and dysmorphic features that has_material_basis_in heterozygous mutation in the SRRM2 gene on chromosome 16p13. |
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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 72 | 1 | for disease ribbon | autosomal dominant intellectual developmental disorder 72 | 1 | model of | autosomal dominant intellectual developmental disorder 72 | 1 |
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