low-frequency sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of sensorineural hearing impairment that affects primarily the lower frequencies. (Human Phenotype Ontology, HP_0008573)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008573
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Genes

1 genes associated with the low-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
WFS1 Wolfram syndrome 1 (wolframin)