Brunner Syndrome

Term ID

DOID:0060693

Synonyms

• monoamine oxidase A deficiency

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. (2)

References

• ICD10CM:E70.8
• MESH:C563156
• OMIM:300615
• ORDO:3057

Ontology

Human Disease   ( DOID:0060693 )