empty sella syndrome Gene Set

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

17 genes co-occuring with the disease empty sella syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRL prolactin 1.64936
TRH thyrotropin-releasing hormone 1.41095
POMC proopiomelanocortin 1.21825
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 0.813873
ACOT13 acyl-CoA thioesterase 13 0.693499
MAP9 microtubule-associated protein 9 0.67551
CD3D CD3d molecule, delta (CD3-TCR complex) 0.663578
AVP arginine vasopressin 0.586665
ADO 2-aminoethanethiol (cysteamine) dioxygenase 0.47753
INS insulin 0.392629
HSPG2 heparan sulfate proteoglycan 2 0.366671
PGK1 phosphoglycerate kinase 1 0.347879
CRH corticotropin releasing hormone 0.335412
GH1 growth hormone 1 0.309566
IGF1 insulin-like growth factor 1 (somatomedin C) 0.272953
TF transferrin 0.164786
PPY pancreatic polypeptide 0.159658