splenic rupture Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A breach of the capsule of the spleen. (Human Phenotype Ontology, HP_0012223)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012223
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Genes

3 genes associated with the splenic rupture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain