Coffin-Siris syndrome 1
Also known as: ARID1B-related BAFopathy, COFFIN-SIRIS syndrome, COFFIN-SIRIS syndrome 1, CSS, CSS1, Coffin-Siris syndrome 1, MRD12, autosomal dominant mental retardation 12, fifth digit syndrome, hypertrichosis, hyperkeratosis, intellectual disability, and distinctive facial features, hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features, intellectual disability, autosomal dominant 12, mental retardation, autosomal dominant 12, mental retardation, autosomal dominant type 12



