| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormal (non-anatomic) location of the spleen. (Human Phenotype Ontology, HP_0010452) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010452 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the ectopia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ACVR2B | activin A receptor, type IIB |
