Disease: Ataxias, Hereditary ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		0.010 Biomarker disease BEFREE Besides, attention should be paid to distinguish Perrault syndrome from D-bifunctional protein deficiency and hereditary ataxia. 28830375 2017