hypoalphalipoproteinemia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An decreased concentration of high-density lipoprotein cholesterol in the blood. (Human Phenotype Ontology, HP_0003233)
External Link http://www.omim.org/entry/604091
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Genes

1 genes associated with the hypoalphalipoproteinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
APOA1 apolipoprotein A-I