Human genes for Brunner Syndrome
Brunner Syndrome [DOID:0060693]
An amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11.
Synonyms: Brunner Syndrome, Brunner disease, Brunner disorder, Brunner Syndromes, DOID:0060693 ...