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 ...