Coffin-Siris syndrome 8

MONDO:0032702

Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCC2 gene.

Also known as: SMARCC2-related BAFopathy, COFFIN-SIRIS SYNDROME 8, CSS8

0 clinical trials for this condition and its sub-types, 0 tagged with Coffin-Siris syndrome 8 itself.

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