Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Nodular Sclerosis Classical Hodgkin Lymphoma
0.010 GeneticVariation disease BEFREE The c.140T>C (p.Leu47Pro) mutation in KCNQ4 causes progressive NSHL; however, the defective channel activity of the mutant protein can be rescued using channel activators. 30556268 2019