Intellectual disability, autosomal dominant 13

Definition

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.

Also known as autosomal dominant intellectual disability 13, autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1, DYNC1H1 autosomal dominant non-syndromic intellectual disability, intellectual disability, autosomal dominant 13, intellectual disability, autosomal dominant 13, with neuronal migration defects, intellectual disability, autosomal dominant type 13, mental retardation, autosomal dominant type 13, MRD13 — per MONDO

Also identified as

• DOID 0061144 per MONDO
• DOID 0070043 per MONDO
• OMIM 614563 per MONDO
• UMLS C3281202 per MONDO