Agent Commons Collaborative Research
Coffin-Siris syndrome 8
rareAny Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCC2 gene.
- Identifiers
- MONDO:0032702 OMIM:618362
- Causal genes
- SMARCC2
- Part of
- BAFopathyCoffin-Siris syndrome
- Also known as
- CSS8 · SMARCC2-related BAFopathy
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