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General Information
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| Term |
autosomal recessive intellectual developmental disorder 73 |
ID (Ontology) |
DOID:0081233 (Human Disease) |
| Definition |
An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay with hypotonia and mildly delayed walking, impaired intellectual development with poor or absent speech, and mildly dysmorphic features and that has_material_basis_in homozygous mutation in the NAA20 gene on chromosome 20p11. |
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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 recessive intellectual developmental disorder 73 | 3 | for disease ribbon | autosomal recessive intellectual developmental disorder 73 | 3 | model of | autosomal recessive intellectual developmental disorder 73 | 3 |
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