autosomal dominant intellectual developmental disorder 13 (DOID:0070043)
Alliance: disease page
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.