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autosomal dominant intellectual developmental disorder 13 (DOID:0070043)
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Synonyms: autosomal dominant mental retardation 13; autosomal dominant non-syndromic intellectual disability 13; mental retardation, autosomal dominant 13, with neuronal migration defects; MRD13
Alt IDs: OMIM:614563
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31.

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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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12/10/2024
MGI 6.24 		The Jackson Laboratory