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complex cortical dysplasia with other brain malformations 13 (DOID:0070043)
Alliance: disease page
Synonyms: autosomal dominant intellectual developmental disorder 13; autosomal dominant mental retardation 13; autosomal dominant non-syndromic intellectual disability 13; CDCBM13; mental retardation, autosomal dominant 13, with neuronal migration defects; MRD13
Alt IDs: OMIM:614563, UMLS_CUI:C3281202
Definition: A complex cortical dysplasia with other brain malformations characterized by global developmental delay with impaired intellectual development that has_material_basis_in heterozygous mutation in 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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09/15/2026
MGI 6.29 		The Jackson Laboratory