cardiovascular calcification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal calcification in the cardiovascular system. (Human Phenotype Ontology, HP_0011915)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011915
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Genes

11 genes associated with the cardiovascular calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FBN1 fibrillin 1
FGF23 fibroblast growth factor 23
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GBA glucosidase, beta, acid
HGD homogentisate 1,2-dioxygenase
KL klotho
NT5E 5'-nucleotidase, ecto (CD73)
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SMAD6 SMAD family member 6