autosomal dominant intellectual developmental disorder 67 Disease Ontology Browser

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autosomal dominant intellectual developmental disorder 67 (DOID:0061040)
Alliance: disease page
Alt IDs: OMIM:619927
Definition: An autosomal dominant intellectual developmental disorder characterized by global developmental delay with variably impaired intellectual development apparent from infancy or early childhood that has_material_basis_in heterozygous mutation in the GRIA1 gene on chromosome 5q33.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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