intracranial hypotension Gene Set

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

18 genes co-occuring with the disease intracranial hypotension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
EBNA1BP2 EBNA1 binding protein 2 1.79616
HSF4 heat shock transcription factor 4 1.38036
FXYD5 FXYD domain containing ion transport regulator 5 1.26909
SCGB1D1 secretoglobin, family 1D, member 1 1.22475
KLK8 kallikrein-related peptidase 8 0.992752
GPANK1 G patch domain and ankyrin repeats 1 0.767985
GJB6 gap junction protein, beta 6, 30kDa 0.725311
NEUROD1 neuronal differentiation 1 0.643404
CD6 CD6 molecule 0.569163
TGFBR2 transforming growth factor, beta receptor II (70/80kDa) 0.534248
TF transferrin 0.468819
CABIN1 calcineurin binding protein 1 0.466172
ALB albumin 0.453716
LCK LCK proto-oncogene, Src family tyrosine kinase 0.435275
PTCH1 patched 1 0.433772
CST3 cystatin C 0.377773
NF1 neurofibromin 1 0.223509
NOTCH1 notch 1 0.211261