Cerebrooculofacioskeletal Syndrome 3, also known as cofs3, is related to cerebrooculofacioskeletal syndrome and xeroderma pigmentosum-cockayne syndrome complex, and has symptoms including edema An important gene associated with Cerebrooculofacioskeletal Syndrome 3 is ERCC5 (ERCC Excision Repair 5, Endonuclease). Affiliated tissues include skin and brain, and related phenotypes are cleft palate and microphthalmia