Intellectual disability, autosomal recessive 18

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MED23 gene.

Also known as: MED23 autosomal recessive non-syndromic intellectual disability, autosomal recessive non-syndromic intellectual disability caused by mutation in MED23, intellectual developmental disorder, autosomal recessive 18, with or without epilepsy, intellectual disability, autosomal recessive 18, intellectual disability, autosomal recessive type 18, mental retardation, autosomal recessive type 18, MED23, MRT18

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal recessive 18 itself.