Monarch Disease Ontology entry MONDO_0013657 (intellectual disability, autosomal dominant 10) is any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene. Also known as: CACNG2 autosomal dominant non-syndromic intellectual disability, MRD10, autosomal dominant intellectual disability 10, autosomal dominant mental retardation 10, autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2, intellectual disability, autosomal dominant type 10, mental retardation, autosomal dominant type 10.