Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
Acute Motor Axonal Neuropathy
0.010 GeneticVariation disease BEFREE In NOD2 (Arg702Trp and Gly908Arg) polymorphisms, only heterozygous genotype (Arg/Trp and Gly/Arg) showed significant association with GBS (p=0.001 and p=0.01 respectively); subtypes AMAN, acute motor-sensory axonal neuropathy (AMSAN) and AIDP showed association with heterozygote Arg702Trp (p=0.001; p=0.029 and p=0.001 respectively) whereas only AIDP was associated with heterozygote genotype Gly908Arg (p=0.003). 27000222 2016