has material basis in germline mutation in ARID1A autosomal dominant disease intellectual disability, autosomal dominant 14 https://github.com/monarch-initiative/mondo/issues/3939 https://www.malacards.org/card/coffin_siris_syndrome_2 MEDGEN:766161 GARD:0015820 mental retardation, autosomal dominant 14 intellectual disability, autosomal dominant type 14 mental retardation, autosomal dominant type 14 autosomal dominant intellectual disability 14 MRD14 ARID1A-related BAFopathy UMLS:C3553247 MONDO:0013819 intellectual disability, autosomal dominant 14 Coffin-Siris syndrome caused by mutation in ARID1A DOID:0070044 Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID1A gene. OMIM:614607 ARID1A Coffin-Siris syndrome CSS2 Coffin-Siris syndrome autosomal dominant non-syndromic intellectual disability BAFopathy