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Metadata
ID	DOID:0060693
Name	Brunner Syndrome
Definition	An amino acid metabolic disorder characterized by recessive X-linked inheritance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11. https://www.ncbi.nlm.nih.gov/pubmed/8211186, https://www.ncbi.nlm.nih.gov/pubmed/8503438
Xrefs	ICD10CM:E70.8 MESH:C563156 MIM:300615 ORDO:3057
Subsets	DO_rare_slim
Synonyms	monoamine oxidase A deficiency [EXACT]
Parent Relationships	is_a amino acid metabolic disorder is_a X-linked recessive disease