pulmonary venoocclusive disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_5453)
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17 genes co-occuring with the disease pulmonary venoocclusive disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
EIF2AK4 eukaryotic translation initiation factor 2 alpha kinase 4 2.04146
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase) 1.50798
KCNK3 potassium channel, two pore domain subfamily K, member 3 1.33545
ONECUT3 one cut homeobox 3 1.21392
CD274 CD274 molecule 1.0324
APLNR apelin receptor 0.95996
GNLY granulysin 0.942027
NPPB natriuretic peptide B 0.893769
ACVRL1 activin A receptor type II-like 1 0.756156
SNRNP70 small nuclear ribonucleoprotein 70kDa (U1) 0.716021
GAA glucosidase, alpha; acid 0.604591
ERAS ES cell expressed Ras 0.567609
PDGFRB platelet-derived growth factor receptor, beta polypeptide 0.559062
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 0.522273
CAV1 caveolin 1, caveolae protein, 22kDa 0.42664
ASRGL1 asparaginase like 1 0.400826
PDGFB platelet-derived growth factor beta polypeptide 0.39598