normal pressure hydrocephalus 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_1572)
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Genes

69 genes co-occuring with the disease normal pressure hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SNPH syntaphilin 1.8701
LRG1 leucine-rich alpha-2-glycoprotein 1 1.67367
SFMBT1 Scm-like with four mbt domains 1 1.34156
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5 1.16435
CEBPZ CCAAT/enhancer binding protein (C/EBP), zeta 1.10048
AAMP angio-associated, migratory cell protein 1.00161
GLRB glycine receptor, beta 0.99908
ASPSCR1 alveolar soft part sarcoma chromosome region, candidate 1 0.994861
PRAMEF9 PRAME family member 9 0.916375
VIT vitrin 0.870415
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 0.844621
GLRA1 glycine receptor, alpha 1 0.832329
HCRT hypocretin (orexin) neuropeptide precursor 0.814283
MAPT microtubule-associated protein tau 0.792541
FXYD5 FXYD domain containing ion transport regulator 5 0.776568
APOE apolipoprotein E 0.736243
PTGDS prostaglandin D2 synthase 21kDa (brain) 0.731786
NPY neuropeptide Y 0.700722
NPFF neuropeptide FF-amide peptide precursor 0.685091
YWHAB tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta 0.668742
DBI diazepam binding inhibitor (GABA receptor modulator, acyl-CoA binding protein) 0.634349
PYY peptide YY 0.594064
VIP vasoactive intestinal peptide 0.590558
MRS2 MRS2 magnesium transporter 0.574217
NPS neuropeptide S 0.570329
CHAT choline O-acetyltransferase 0.552851
E2F5 E2F transcription factor 5, p130-binding 0.541992
MBP myelin basic protein 0.52536
IRF6 interferon regulatory factor 6 0.513417
PRB3 proline-rich protein BstNI subfamily 3 0.506123
KLK8 kallikrein-related peptidase 8 0.502292
MLX MLX, MAX dimerization protein 0.502292
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5 0.499231
ALB albumin 0.49274
MRPL49 mitochondrial ribosomal protein L49 0.485125
BDKRB2 bradykinin receptor B2 0.468441
PSEN1 presenilin 1 0.46466
SST somatostatin 0.458996
HPN hepsin 0.446558
PRRC2A proline-rich coiled-coil 2A 0.423265
TIMP4 TIMP metallopeptidase inhibitor 4 0.415024
APOD apolipoprotein D 0.413901
TGFB2 transforming growth factor, beta 2 0.412031
MAPK14 mitogen-activated protein kinase 14 0.388538
AVP arginine vasopressin 0.387794
TTR transthyretin 0.387051
EFS embryonal Fyn-associated substrate 0.376661
ADORA2A adenosine A2a receptor 0.32373
EXTL3 exostosin-like glycosyltransferase 3 0.323365
AQP4 aquaporin 4 0.310652
IL10 interleukin 10 0.304864
ENO2 enolase 2 (gamma, neuronal) 0.303781
AMBP alpha-1-microglobulin/bikunin precursor 0.300533
ADRA1D adrenoceptor alpha 1D 0.299452
AQP1 aquaporin 1 (Colton blood group) 0.289027
CNTF ciliary neurotrophic factor 0.26514
GCH1 GTP cyclohydrolase 1 0.26266
DES desmin 0.256652
AHSG alpha-2-HS-glycoprotein 0.251015
FABP3 fatty acid binding protein 3, muscle and heart 0.244696
XRCC6 X-ray repair complementing defective repair in Chinese hamster cells 6 0.240847
L1CAM L1 cell adhesion molecule 0.233878
TF transferrin 0.228679
CLU clusterin 0.197742
GAL galanin/GMAP prepropeptide 0.197742
AQP2 aquaporin 2 (collecting duct) 0.194232
BDNF brain-derived neurotrophic factor 0.188632
TRIM37 tripartite motif containing 37 0.172799
VIM vimentin 0.160948