DISEASES

Disease-gene associations mined from literature

Human genes for White-Sutton syndrome

White-Sutton syndrome [DOID:0070067]

An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3.

Synonyms:  White-Sutton syndrome,  White-Sutton disorder,  DOID:0070067,  WhiteSutton syndrome,  White-Sutton disease ...