FXN, frataxin, 2395

N. diseases: 220; N. variants: 21
Disease: Pallidoluysian degeneration ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393578
Disease: Pallidoluysian degeneration
Pallidoluysian degeneration 		0.010 Biomarker disease BEFREE We investigated the relative prevalence of SCA1-3, 6-8, 12, 17; dentate-rubro-pallidoluysian atrophy; and Friedreich's ataxia (FRDA) in Serbian patients with adult-onset (>20 years of age) hereditary and sporadic SCAs, and compared clinical features of patients with genetically confirmed SCAs. 16149098 2006