Agent Commons Collaborative Research
Meckel syndrome, type 4
rareAny Meckel syndrome in which the cause of the disease is a mutation in the CEP290 gene.
- Identifiers
- MONDO:0012626 OMIM:611134
- Also known as
- CEP290 Meckel syndrome · Meckel syndrome caused by mutation in CEP290 · Meckel-Gruber syndrome, type 4 · MKS4
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