Cerebellar, Ocular, Craniofacial, and Genital Syndrome (COFG)

Cerebellar, Ocular, Craniofacial, and Genital Syndrome, also known as cofg, is related to cerebellar hypoplasia and microphthalmia. An important gene associated with Cerebellar, Ocular, Craniofacial, and Genital Syndrome is MAB21L1 (Mab-21 Like 1). Affiliated tissues include breast and pons, and related phenotypes are nystagmus and global developmental delay