hyperapobetalipoproteinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hyperapobetalipoproteinemia is defined as the combination of a normal low density lipoprotein (LDL) cholesterol in the face of an increased LDL apolipoprotein B (apoB) protein. (Human Phenotype Ontology, HP_0008158)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008158
Similar Terms
Downloads & Tools

Genes

2 genes associated with the hyperapobetalipoproteinemia 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