| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001747 |
| Similar Terms | |
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4 genes associated with the accessory spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
