Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant ATP6V1B2 disease C2675730 CausalMutation 0.62 disgenet
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant ATP6V1B2 disease C2675730 Biomarker 0.62 disgenet
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant ATP6V1B2 disease C2675730 GermlineCausalMutation 0.62 disgenet
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant ATP6V1B2 disease C2675730 GeneticVariation 0.62 disgenet
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