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 CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegia. 27292318 2016
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 Biomarker phenotype HPO