Human genes for Coffin-Siris syndrome 4
Coffin-Siris syndrome 4 [DOID:0070046]
A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of SMARCA4 on chromosome 19p13.2.
Synonyms: Coffin-Siris syndrome 4, CoffinSiris syndrome 4, DOID:0070046, autosomal dominant mental retardation 16, CSS4 ...