deafness, autosomal dominant 2a Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/600101
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Genes

1 genes associated with the deafness, autosomal dominant 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4