Disease: Dystonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013421
Disease: Dystonia
Dystonia 		0.220 Biomarker phenotype BEFREE Mutations in Atcay/ATCAY have been identified as causative of cerebellar disorders such as the rare hereditary disease Cayman ataxia in humans, generalized dystonia in the dystonic (dt) rat, and marked motor defects in three ataxic mouse lines. 23226316 2012
CUI: C0013421
Disease: Dystonia
Dystonia 		0.220 Biomarker phenotype RGD Caytaxin deficiency causes generalized dystonia in rats. 16246457 2005
CUI: C0013421
Disease: Dystonia
Dystonia 		0.220 Biomarker phenotype BEFREE Caytaxin deficiency causes generalized dystonia in rats. 16246457 2005