|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of the cochlea, a spiral shaped cavity in the inner ear, owing to a developmental defect. (Human Phenotype Ontology, HP_0011395)|
|Downloads & Tools|
2 genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.