accessory spleen Gene Set

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
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Genes

4 genes associated with the accessory spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
HYLS1 hydrolethalus syndrome 1
MKS1 Meckel syndrome, type 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog