Intellectual disability, autosomal dominant 14

MONDO:0013819

Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID1A gene.

Also known as: ARID1A Coffin-Siris syndrome, ARID1A-related BAFopathy, CSS2, Coffin-Siris syndrome caused by mutation in ARID1A, MRD14, autosomal dominant intellectual disability 14, intellectual disability, autosomal dominant 14, intellectual disability, autosomal dominant type 14

38 clinical trials for this condition and its sub-types.

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