DISEASES

Disease-gene associations mined from literature

Human genes for Mowat-Wilson syndrome

Mowat-Wilson syndrome [DOID:0060485]

A syndrome characterized by distinctive facial features, intellectual disability, delayed development, Hirschsprung disease and has_material_basis_in de novo heterozygous mutation in the ZEB2 gene on chromosome 2q22.

Synonyms:  Mowat-Wilson syndrome,  DOID:0060485,  MowatWilson syndrome,  Mowat-Wilson disease,  Mowat-Wilson disorder ...