pituitary apoplexy Gene Set

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

19 genes co-occuring with the disease pituitary apoplexy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 1.43727
TRH thyrotropin-releasing hormone 1.36335
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 1.33894
PRL prolactin 1.32148
GSAP gamma-secretase activating protein 0.737054
AIP aryl hydrocarbon receptor interacting protein 0.683493
IGF1 insulin-like growth factor 1 (somatomedin C) 0.647743
SST somatostatin 0.584719
SETD2 SET domain containing 2 0.530381
SETD1A SET domain containing 1A 0.493122
CRH corticotropin releasing hormone 0.469197
INS insulin 0.428516
NFIC nuclear factor I/C (CCAAT-binding transcription factor) 0.357814
IVD isovaleryl-CoA dehydrogenase 0.357077
NFIX nuclear factor I/X (CCAAT-binding transcription factor) 0.355604
OR4F29 olfactory receptor, family 4, subfamily F, member 29 0.287235
MEN1 multiple endocrine neoplasia I 0.282225
AVP arginine vasopressin 0.239101
IVL involucrin 0.217012