abnormal circulating creatinine level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal concentration of creatinine in the blood. (Human Phenotype Ontology, HP_0012100)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012100
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7 genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
FAN1 FANCD2/FANCI-associated nuclease 1
HNF1B HNF1 homeobox B
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
INVS inversin
MUC1 mucin 1, cell surface associated
WDR19 WD repeat domain 19