Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
0.010 GeneticVariation disease BEFREE We conclude that mutations of the puratrophin-1 gene are not a common cause of hereditary ataxia in our Caucasian population. 16491300 2006