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| Term | neurodevelopmental disorder with language delay and seizures | ID (Ontology) | DOID:0070444 (Human Disease) | |||||||||||||||||||||||
| Definition | An autosomal recessive intellectual developmental disorder characterized by early-onset seizures and global developmental delay with intellectual disability and speech delay that has_material_basis_in homozygous or compound heterozygous mutation in the TIAM1 gene on chromosome 21q22. | |||||||||||||||||||||||||
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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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autosomal recessive disease__ intellectual disability______| autosomal recessive intellectual developmental disorder |__neurodevelopmental disorder with language delay and seizures 12 rec. |
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| Is a | autosomal recessive intellectual developmental disorder | ||
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| MIM:619908 | |||