Intellectual Developmental Disorder, Autosomal Dominant 68 (MRD68)

Intellectual Developmental Disorder, Autosomal Dominant 68, is also known as mrd68. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 68 is KMT2B (Lysine Methyltransferase 2B). Affiliated tissues include eye and brain, and related phenotypes are intellectual disability and nystagmus