Disease: Ataxia, Motor ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0278161
Disease: Ataxia, Motor
Ataxia, Motor 		0.300 Biomarker phenotype CTD_human Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A. 17376154 2007