|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form of sensorineural deafness with either congenital onset or infantile onset, i.e., before the acquisition of speech. (Human Phenotype Ontology, HP_0000399)|
|Downloads & Tools|
4 genes associated with the prelingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.