Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene. The disease is intellectual disability, autosomal dominant 13 (MONDO_0013805, a Monarch Disease Ontology id). Also known as: DYNC1H1 autosomal dominant non-syndromic intellectual disability, MRD13, autosomal dominant intellectual disability 13, autosomal dominant mental retardation 13, autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1, intellectual disability, autosomal dominant 13, with neuronal migration defects, intellectual disability, autosomal dominant type 13, mental retardation, autosomal dominant 13, with neuronal migration defects.