cranioectodermal dysplasia 3 (Monarch Disease Ontology term MONDO_0013573) is 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 caused by mutation in IFT43.