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 presence of the GIPC3 mutations in only one of 100 Saudi families with congenital NSHL suggests that it appears to be a rare cause of familial or sporadic deafness in this population. 23510777 2013