|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A morphological abnormality of the vestibule, the central part of the osseous labyrinth that is situated medial to the tympanic cavity, behind the cochlea, and in front of the semicircular canals. (Human Phenotype Ontology, HP_0011376)|
|Downloads & Tools|
4 genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.