14569121-n 'a rare inherited disorder of copper metabolism';
 
Chinese (simplified) 肌震颤性综合征 , 肝豆状核变性 , 威尔森氏症
English hepatolenticular degeneration , Wilson's disease
Japanese 肝レンズ核変性症
Definitions
English
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
Indonesian
suatu gangguan dalam metabolisme tembaga yang jarang dan diwariskan
Relations
Hypernym: genetic_disease
Semantic Field: staten
External Links

SUMO: ⊂ DiseaseOrSyndrome

TempoWN: (Past: 0.000; Present: 0.003; Future: 0.000)

SentiWN: (+0.00 -0.00) MLSentiCon: (+0.00 -0.38)


Langs:

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Maintainer: Francis Bond <bond@ieee.org>