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Disease Info Card
Idiopathic Hypogonadotropic Hypogonadism
Information about Idiopathic Hypogonadotropic Hypogonadism: 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 Idiopathic Hypogonadotropic Hypogonadism
Most recent studies have shown that Idiopathic Hypogonadotropic Hypogonadism shares some biological mechanisms with amenorrhea, androgen-deficiency, anosmia, cryptorchidism, delayed-puberty, hereditary-diseases, hypogonadism, hypogonadotropic-hypogonadism, hypopituitarism, hypothalamic-amenorrhea, infertility, kallmann-syndrome, klinefelter-syndrome, male-infertility, neoplasms, olfaction-disorders, pituitary-diseases, precocious-puberty, testicular-hypogonadism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Idiopathic Hypogonadotropic Hypogonadism, and have been seen in publications frequently: Cell Migration, Chromatin Remodeling, Developmental Process, Follicle-stimulating Hormone Secretion, Glycosylation, Gonadotropin Secretion, Hormone Secretion, Inhibin Secretion, Localization, Luteinizing Hormone Secretion, Menopause, Neuron Development, Neuron Migration, Ovulation, Pathogenesis, Prolactin Secretion, Secretion, Spermatogenesis, Thelarche, Uterus Development
Quite a number of genes have been found to play important roles in Idiopathic Hypogonadotropic Hypogonadism, such as BRD2, COL18A1, FGF8, FGFR1, GNRH1, GNRHR, IHH, KISS1, KISS1R, NR0B1, OXSM, PLOD1, PRL, PROK2, PROKR2, TAC3, TACR3. 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.