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
Inggeris hepatolenticular degeneration , Wilson's disease
Japanese 肝レンズ核変性症
Definitions
Bahasa Indonesia
suatu gangguan dalam metabolisme tembaga yang jarang dan diwariskan
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

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>