?deafness, autosomal recessive 102 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615974
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1 genes associated with the ?deafness, autosomal recessive 102 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
EPS8 epidermal growth factor receptor pathway substrate 8