Intellectual disability, autosomal dominant 15

MONDO:0013820

Any 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

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 15 itself.

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↑ Autosomal dominant disease (699) ↑ Coffin-Siris syndrome (1) ↑ BAFopathy (0)

Including sub-types (0) Tagged with Intellectual disability, autosomal dominant 15 (0)

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