|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence of the inner ear due to a developmental defect. (Human Phenotype Ontology, HP_0011372)|
|Downloads & Tools|
1 genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|FGF3||fibroblast growth factor 3|