|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal elevation of the C-reactive protein level in serum. (Human Phenotype Ontology, HP_0011227)|
|Downloads & Tools|
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.
|NLRP12||NLR family, pyrin domain containing 12|