Disease: Dystonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 GeneticVariation phenotype BEFREE These results show that the 10197G>A mutation in the mitochondrial ND3 gene should be considered as a common mtDNA mutation responsible for LS and dystonia. 17152068 2007
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 GeneticVariation phenotype LHGDN These results show that the 10197G>A mutation in the mitochondrial ND3 gene should be considered as a common mtDNA mutation responsible for LS and dystonia. 17152068 2007
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 Biomarker phenotype HPO