|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomalous concentration of testosterone in the blood. (Human Phenotype Ontology, HP_0030087)|
|Downloads & Tools|
1 genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SLC39A4||solute carrier family 39 (zinc transporter), member 4|