Brunner Syndrome (Q4979092)
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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
- 单胺氧化酶A缺乏症
- Brunner综合征
- monoamine oxidase A deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Brunner Syndrome |
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 |
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Wikipedia(10 entries)
- arwiki متلازمة برونر
- dewiki Monoaminoxidase-A-Mangel
- enwiki Brunner syndrome
- eswiki Síndrome de Brunner
- fawiki سندرم برونر
- fiwiki Brunnerin oireyhtymä
- jawiki ブルンナー症候群
- plwiki Zespół Brunnera
- trwiki Brunner sendromu
- ukwiki Синдром Бруннера