Disease: Deafness, Autosomal Dominant 2B ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Deafness, Autosomal Dominant 2B
CUI: C2675236
Disease: Deafness, Autosomal Dominant 2B
0.700 GeneticVariation UNIPROT Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. 9843210 1998