Cranioectodermal dysplasia 3

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

59 clinical trials for this condition and its sub-types.