bn:00545792n
Noun Concept
Categories: Amino acid metabolism disorders, Articles with short description, Rare syndromes
EN
Brunner syndrome  Brunner综合征  Monoamine oxidase A (MAOA) deficiency  monoamine oxidase A deficiency  单胺氧化酶A缺乏症
EN
Brunner syndrome is a rare genetic disorder associated with a mutation in the MAOA gene. Wikipedia
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EN
Brunner syndrome is a rare genetic disorder associated with a mutation in the MAOA gene. Wikipedia
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 location Xp11 Wikidata
A genetic disorder associated with mild intellectual disability, impulsiveness, sudden changes of mood, and aggressive and antisocial behaviours. Wiktionary
GENETIC ASSOCIATION