Cranioectodermal dysplasia 3

MONDO:0013573

Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT43 gene.

Also known as: Cranioectodermal dysplasia type 3, IFT43 cranioectodermal dysplasia, cranioectodermal dysplasia 3, cranioectodermal dysplasia caused by mutation in IFT43, CED3, CRANIOECTODERMAL dysplasia 3

2 clinical trials for this condition and its sub-types, 0 tagged with Cranioectodermal dysplasia 3 itself.

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↑ Cranioectodermal dysplasia (0)

Including sub-types (2) Tagged with Cranioectodermal dysplasia 3 (0)

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