Cranioectodermal dysplasia 2

Definition

Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the WDR35 gene.

Also known as cranioectodermal dysplasia 2, cranioectodermal dysplasia caused by mutation in WDR35, Cranioectodermal dysplasia type 2, WDR35 cranioectodermal dysplasia, WDR35-related cranioectodermal dysplasia — per MONDO

Also identified as

• DOID 0080804 per MONDO
• OMIM 613610 per MONDO
• UMLS C3150874 per MONDO