recurrent hypersomnia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A sleep disorder that involves recurring bouts of excessive amounts of sleepiness. (Human Disease Ontology, DOID_8619)
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Genes

12 genes co-occuring with the disease recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HCRT hypocretin (orexin) neuropeptide precursor 1.68136
RPS6KB2 ribosomal protein S6 kinase, 70kDa, polypeptide 2 1.48296
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1 1.13247
HLA-DQB3 major histocompatibility complex, class II, DQ beta 3 1.01512
HLA-C major histocompatibility complex, class I, C 0.909787
RHCE Rh blood group, CcEe antigens 0.62885
CORT cortistatin 0.571884
TPH1 tryptophan hydroxylase 1 0.505356
RHD Rh blood group, D antigen 0.500761
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 0.458996
TRH thyrotropin-releasing hormone 0.404184
COMT catechol-O-methyltransferase 0.245046