PAX3, paired box 3, 5077

N. diseases: 257; N. variants: 62
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome
0.010 GeneticVariation disease BEFREE WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures. 20972738 2010