Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT43 gene.
Comprehensive, easy-to-understand information about this condition
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cranioectodermal dysplasia 2
MONDO:0013323
cranioectodermal dysplasia 4
MONDO:0013719
short-rib thoracic dysplasia 16 with or without polydactyly
MONDO:0014915
cranioectodermal dysplasia 1
MONDO:0021093
cranioectodermal dysplasia 5
MONDO:0976269
cranioectodermal dysplasia 6
MONDO:0979883