|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An Abnormality of cortical bone leading to an abnormal thickness of the cortex of affected bones. (Human Phenotype Ontology, HP_0100039)|
|Downloads & Tools|
6 genes associated with the thickened cortex of bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.