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 Biomarker phenotype BEFREE The novel myoclonus-dystonia genes KCTD17 and CACNA1B also implicate abnormal calcium signaling in dystonia. 26991507 2016
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 Biomarker phenotype HPO