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Disease Ontology Browser
Brunner Syndrome (DOID:0060693)
Alliance: disease page
Synonyms: monoamine oxidase A deficiency
Alt IDs: OMIM:300615, ICD10CM:E70.8, MESH:C563156, ORDO:3057
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.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory