high pressure neurological syndrome Gene Set

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

11 genes co-occuring with the disease high pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PGLYRP3 peptidoglycan recognition protein 3 2.06171
APEH acylaminoacyl-peptide hydrolase 1.77812
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit 1.2582
NPEPPS aminopeptidase puromycin sensitive 1.0711
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9 1.01427
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 1.00372
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 0.80936
MGAM maltase-glucoamylase 0.727738
CA4 carbonic anhydrase IV 0.703938
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic 0.616703
TH tyrosine hydroxylase 0.305948