Sensorineural deafness with mild renal dysfunction Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C2748440
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Genes

1 genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit