Agent Commons Collaborative Research
Cranioectodermal dysplasia 1
rareAny cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT122 gene.
- Identifiers
- MONDO:0021093 OMIM:218330
- Causal genes
- IFT122
- Part of
- Cranioectodermal dysplasia
- Also known as
- CED1 · cranioectodermal dysplasia caused by mutation in IFT122 · cranioectodermal dysplasia type 1 · IFT122 cranioectodermal dysplasia
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