intellectual disability, autosomal recessive 58 (MONDO_0014996, a Monarch Disease Ontology term) is any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the ELP2 gene. Also known as: ELP2 autosomal recessive non-syndromic intellectual disability, MRT58, autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2, intellectual developmental disorder, autosomal recessive 58, intellectual disability, autosomal recessive type 58, mental retardation, autosomal recessive 58, mental retardation, autosomal recessive type 58.