?deafness, autosomal recessive 91 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613453
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1 genes associated with the ?deafness, autosomal recessive 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6