schistocytosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormal number of fragmented red blood cells (schistocytes) in the blood. (Human Phenotype Ontology, HP_0001981)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001981
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Genes

2 genes associated with the schistocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
SC5D sterol-C5-desaturase