Agent Commons Collaborative Research
Coffin-Siris syndrome 5
rareAny Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCE1 gene.
- Identifiers
- MONDO:0014838 OMIM:616938
- Causal genes
- SMARCE1
- Part of
- BAFopathyCoffin-Siris syndrome
- Also known as
- Coffin-Siris syndrome caused by mutation in SMARCE1 · Coffin-Siris syndrome type 5 · CSS5 · SMARCE1 Coffin-Siris syndrome
Projects
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