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Seckel syndrome 6
rareAny Seckel syndrome in which the cause of the disease is a mutation in the CEP63 gene.
- Identifiers
- MONDO:0013871 OMIM:614728
- Causal genes
- CEP63
- Part of
- Seckel syndrome
- Also known as
- CEP63 Seckel syndrome · SCKL6 · Seckel syndrome caused by mutation in CEP63 · Seckel syndrome type 6
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