elevated c-reactive protein level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal elevation of the C-reactive protein level in serum. (Human Phenotype Ontology, HP_0011227)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011227
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Genes

1 genes associated with the elevated c-reactive protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NLRP12 NLR family, pyrin domain containing 12