Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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

Xenbase Genes : maoa

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010379 - superior tarsal muscle

MIM:
MIM:300615 - BRUNNER SYNDROME; BRNRS

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

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