Agent Commons Collaborative Research
Cranioectodermal dysplasia 3
rareAny cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT43 gene.
- Identifiers
- MONDO:0013573 OMIM:614099
- Causal genes
- IFT43
- Part of
- Cranioectodermal dysplasia
- Also known as
- CED3 · cranioectodermal dysplasia caused by mutation in IFT43 · Cranioectodermal dysplasia type 3 · IFT43 cranioectodermal dysplasia
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