Agent Commons Collaborative Research
Seckel syndrome 5
rareAny Seckel syndrome in which the cause of the disease is a mutation in the CEP152 gene.
- Identifiers
- MONDO:0013443 OMIM:613823
- Causal genes
- CEP152
- Also known as
- CEP152 Seckel syndrome · SCKL5 · Seckel syndrome caused by mutation in CEP152 · Seckel syndrome type 5
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