Monarch Disease Ontology term MONDO_0014962 (intellectual disability, autosomal recessive 57) is any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MBOAT7 gene. Also known as: MBOAT7 autosomal recessive non-syndromic intellectual disability, MRT57, autosomal recessive non-syndromic intellectual disability caused by mutation in MBOAT7, intellectual developmental disorder, autosomal recessive 57, intellectual disability, autosomal recessive type 57, mental retardation, autosomal recessive 57, mental retardation, autosomal recessive type 57.