|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form of sensorineural hearing impairment with infantile onset. (Human Phenotype Ontology, HP_0008610)|
|Downloads & Tools|
1 genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TIMM8A||translocase of inner mitochondrial membrane 8 homolog A (yeast)|