arterial calcification of infancy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A vascular disease that is characterized by generalized calcification of the arterial internal elastic lamina, leading to rupture of the lamina and occlusive changes in the tunica intima with stenosis and decreased elasticity of the vessel wall. (Human Disease Ontology, DOID_0050644)
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Genes

20 genes co-occuring with the disease arterial calcification of infancy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1 2.78678
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6 2.07077
ENTPD5 ectonucleoside triphosphate diphosphohydrolase 5 1.01216
SLC20A2 solute carrier family 20 (phosphate transporter), member 2 0.988535
S100A11 S100 calcium binding protein A11 0.790492
MGP matrix Gla protein 0.629242
FGF23 fibroblast growth factor 23 0.566054
PHEX phosphate regulating endopeptidase homolog, X-linked 0.536957
SPTA1 spectrin, alpha, erythrocytic 1 0.498085
ALPL alkaline phosphatase, liver/bone/kidney 0.401945
CTSK cathepsin K 0.355235
DDIT3 DNA-damage-inducible transcript 3 0.349717
AHSG alpha-2-HS-glycoprotein 0.332852
NT5E 5'-nucleotidase, ecto (CD73) 0.309204
RUNX2 runt-related transcription factor 2 0.289744
ALPPL2 alkaline phosphatase, placental-like 2 0.258064
ALPP alkaline phosphatase, placental 0.257711
AGER advanced glycosylation end product-specific receptor 0.248905
CD36 CD36 molecule (thrombospondin receptor) 0.20229
GBA glucosidase, beta, acid 0.198386