|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Reduced or lacking hair growth in the temporal region (i.e., around the temples on the side of the skull). (Human Phenotype Ontology, HP_0004524)|
|Downloads & Tools|
1 genes associated with the temporal hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|KRT85||keratin 85, type II|