14569121-n 'a rare inherited disorder of copper metabolism';
 
Chinese (simplified) 肌震颤性综合征 , 威尔森氏症 , 肝豆状核变性 , 威尔 森氏症 , 肝豆状 核 变性 , 肌震颤 性 综合 征
Inggeris hepatolenticular degeneration , Wilson's disease
Bahasa Indonesia degenerasi-hepatolentikular , penyakit-wilson , tembaga ..
Japanese 肝レンズ核変性症
Bahasa Malaysia tembaga ..
Definitions
Inggeris
a rare inherited disorder of copper metabolism
copper accumulates in the liver and then in the red blood cells and brain
Japanese
まれな遺伝による銅代謝の疾患
肝臓、そして赤血球と脳に銅が蓄積する
Relations
Hypernym: genetic_disease
Semantic Field: staten
External Links

Langs:

Preferences
(0.03112 seconds)
More detail about the NTUMC+ Open Multilingual Wordnet (0.9)
This project is now integrated in the Extended Open Multilingual Wordnet (0.9)
Maintainer: Francis Bond <bond@ieee.org>