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

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 14 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.