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Summary Literature (0)
MIM:614608 - COFFIN-SIRIS SYNDROME 3; CSS3

Xenbase Genes: smarcb1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013820 - intellectual disability, autosomal dominant 15
MONDO:0015452 - Coffin-Siris syndrome

Disease Ontology (DO):
DOID:0070045 - Coffin-Siris syndrome 3