intermittent jaundice Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Jaundice that is sometimes present, sometimes not. (Human Phenotype Ontology, HP_0001046)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001046
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Genes

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

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1