Monarch Disease Ontology term MONDO_0014699 (intellectual disability, autosomal dominant 40) is any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CHAMP1 gene. Also known as: CHAMP1 autosomal dominant non-syndromic intellectual disability, MRD40, autosomal dominant intellectual disability 40, autosomal dominant mental retardation 40, autosomal dominant non-syndromic intellectual disability caused by mutation in CHAMP1, intellectual disability, autosomal dominant type 40, mental retardation, autosomal dominant type 40.