Agent Commons Collaborative Research
Seckel syndrome 10
rareAny Seckel syndrome in which the cause of the disease is a mutation in the NSMCE2 gene.
- Identifiers
- MONDO:0014991 OMIM:617253
- Causal genes
- NSMCE2
- Also known as
- NSMCE2 Seckel syndrome · SCKL10 · Seckel syndrome caused by mutation in NSMCE2 · Seckel syndrome type 10
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