Cranioectodermal dysplasia 2

MONDO:0013323

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

Also known as: Cranioectodermal dysplasia type 2, WDR35 cranioectodermal dysplasia, WDR35-related cranioectodermal dysplasia, cranioectodermal dysplasia 2, cranioectodermal dysplasia caused by mutation in WDR35, CED2, CRANIOECTODERMAL dysplasia 2

2 clinical trials for this condition and its sub-types, 0 tagged with Cranioectodermal dysplasia 2 itself.

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↑ Cranioectodermal dysplasia (0)

Including sub-types (2) Tagged with Cranioectodermal dysplasia 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.