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Meckel syndrome, type 6
rareAny Meckel syndrome in which the cause of the disease is a mutation in the CC2D2A gene.
- Identifiers
- MONDO:0012848 OMIM:612284
- Causal genes
- CC2D2A
- Also known as
- CC2D2A Meckel syndrome · Meckel syndrome caused by mutation in CC2D2A · MKS6
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