Deafness, Autosomal Dominant 2A Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567441
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Genes

2 genes/proteins associated with the disease Deafness, Autosomal Dominant 2A from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GJB3 gap junction protein, beta 3, 31kDa 2.88009
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4 2.88009