WFS1, wolframin ER transmembrane glycoprotein, 7466

N. diseases: 185; N. variants: 80
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 		0.300 Biomarker disease GENOMICS_ENGLAND Correction: Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease. 30171196 2018