Intellectual disability, autosomal dominant 15
MONDO:0013820Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCB1 gene.
Also known as: COFFIN-SIRIS syndrome 3, CSS3, Coffin-Siris syndrome caused by mutation in SMARCB1, MRD15, SMARCB1 Coffin-Siris syndrome, SMARCB1-related BAFopathy, autosomal dominant intellectual disability 15, intellectual disability, autosomal dominant 15
38 clinical trials for this condition and its sub-types.
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Developmental defect during embryogenesis
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Coffin-Siris syndrome
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