Human genes for White-Sutton syndrome
White-Sutton syndrome [DOID:0070067]
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3.
Synonyms: White-Sutton syndrome, DOID:0070067, WhiteSutton syndrome, White-Sutton disease, White-Sutton disorder ...