Cranioectodermal Dysplasia 2, also known as ced2, is related to camurati-engelmann disease, type 2 and lacrimal duct obstruction. An important gene associated with Cranioectodermal Dysplasia 2 is WDR35 (WD Repeat Domain 35). Affiliated tissues include heart and skin, and related phenotypes are frontal bossing and short neck