Cranioectodermal dysplasia 1

Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT122 gene.

Also known as: Sensenbrenner syndrome, CED1, IFT122 cranioectodermal dysplasia, cranioectodermal dysplasia 1, cranioectodermal dysplasia caused by mutation in IFT122, cranioectodermal dysplasia type 1, Levin syndrome 1

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