Congenital Disorder of Deglycosylation 2 (CDDG2)

Congenital Disorder of Deglycosylation 2, is also known as cddg2. An important gene associated with Congenital Disorder of Deglycosylation 2 is MAN2C1 (Mannosidase Alpha Class 2C Member 1). Affiliated tissues include tongue and brain, and related phenotypes are delayed speech and language development and motor delay