| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A form of sensorineural hearing impairment with infantile onset. (Human Phenotype Ontology, HP_0008610) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008610 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| TIMM8A | translocase of inner mitochondrial membrane 8 homolog A (yeast) |
