hypertensive encephalopathy Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

25 genes co-occuring with the disease hypertensive encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
IK IK cytokine, down-regulator of HLA II 1.05009
ACE angiotensin I converting enzyme 1.00414
REN renin 0.836017
MKKS McKusick-Kaufman syndrome 0.783526
EPO erythropoietin 0.717232
PITX1 paired-like homeodomain 1 0.633169
NTSR1 neurotensin receptor 1 (high affinity) 0.60342
AQP4 aquaporin 4 0.537731
DCX doublecortin 0.533861
ALB albumin 0.51534
WAPAL wings apart-like homolog (Drosophila) 0.514571
CLDN5 claudin 5 0.514186
CX3CL1 chemokine (C-X3-C motif) ligand 1 0.501909
F2RL1 coagulation factor II (thrombin) receptor-like 1 0.490835
HMBS hydroxymethylbilane synthase 0.462394
BDNF brain-derived neurotrophic factor 0.450324
GFAP glial fibrillary acidic protein 0.449194
CX3CR1 chemokine (C-X3-C motif) receptor 1 0.402692
OCLN occludin 0.302337
ADM adrenomedullin 0.276158
PGF placental growth factor 0.212945
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 0.200656
MT3 metallothionein 3 0.198064
NPY neuropeptide Y 0.188938
PDLIM1 PDZ and LIM domain 1 0.165435