|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An accessory spleen is a round, iso-echogenic, homogenic and smooth structure and is seen as a normal variant mostly on the medial contour of the spleen, near the hilus or around the lower pole. This has no pathogenic relevance. (Human Phenotype Ontology, HP_0001747)|
|Downloads & Tools|
4 genes associated with the accessory spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.