Cranioectodermal dysplasia 1

MONDO:0021093

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

2 clinical trials for this condition and its sub-types, 0 tagged with Cranioectodermal dysplasia 1 itself.

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↑ Cranioectodermal dysplasia (0)

Including sub-types (2) Tagged with Cranioectodermal dysplasia 1 (0)

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