|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormally increased ability of the skin to permit light to pass through (translucency) such that subcutaneous structures such as veins display an increased degree of visibility. (Human Phenotype Ontology, HP_0010648)|
|Downloads & Tools|
3 genes associated with the dermal translucency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.