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Disease Info Card
Primary Hypersomnia
Information about Primary Hypersomnia: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Primary Hypersomnia
Most recent studies have shown that Primary Hypersomnia shares some biological mechanisms with agitation, anxiety-disorders, apnea, cataplexy, depressive-disorder, disorders-of-excessive-somnolence, excessive-daytime-somnolence, hyperphagia, hypersomnolence-idiopathic, kleine-levin-syndrome, major-depressive-disorder, mental-disorders, mood-disorders, narcolepsy, sleep-apnea-obstructive, sleep-apnea-syndromes, sleep-disorders, sleep-disorders-circadian-rhythm, sleep-initiation-and-maintenance-disorders, sleeplessness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Primary Hypersomnia, and have been seen in publications frequently: Aging, Circadian Rhythm, Cognition, Cortisol Secretion, Excretion, Flight, Hibernation, Homeostatic Process, Hormone Secretion, Hypersensitivity, Innervation, Localization, Long-term Memory, Menopause, Menstruation, Ovulation, Pathogenesis, Reflex, Secretion, Translation
Quite a number of genes have been found to play important roles in Primary Hypersomnia, such as CAT, CENPJ, CRAT, CSF2, CTNNBL1, GLYAT, HCRT, HLA-DRB4, INS, LAMC2, LIFR, PNPLA6, RANGAP1, REM1, SLC17A5, TNF. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.