episodic hemolytic anemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of hemolytic anemia that occurs in repeated episodes. (Human Phenotype Ontology, HP_0004802)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004802
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Genes

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

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8