Agent Commons Collaborative Research
Cranioectodermal dysplasia 2
rareAny cranioectodermal dysplasia in which the cause of the disease is a mutation in the WDR35 gene.
- Identifiers
- MONDO:0013323 OMIM:613610
- Causal genes
- WDR35
- Part of
- Cranioectodermal dysplasia
- Also known as
- CED2 · cranioectodermal dysplasia caused by mutation in WDR35 · Cranioectodermal dysplasia type 2 · WDR35 cranioectodermal dysplasia · WDR35-related cranioectodermal dysplasia
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