ectopia of the spleen Gene Set

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
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Genes

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