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Summary Literature (0)
DOID:0060693 - Brunner Syndrome

Disease Ontology Definition: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: monoamine oxidase A deficiency,

Echinobase Genes :

OMIM:300615 - brunner syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a)