About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.16
The Jackson Laboratory