{deafness, autosomal recessive 12, modifier of} Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/601386
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Genes

1 genes associated with the {deafness, autosomal recessive 12, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2