|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form of sensorineural hearing impairment that affects primarily the lower frequencies. (Human Phenotype Ontology, HP_0008573)|
|Downloads & Tools|
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.
|WFS1||Wolfram syndrome 1 (wolframin)|