|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the mastoid process, which is the conical prominence projecting from the undersurface of the mastoid portion of the temporal bone. (Human Phenotype Ontology, HP_0000264)|
|Downloads & Tools|
3 genes associated with the abnormality of the mastoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.