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Disease Info Card
Secondary Hypothyroidism
Information about Secondary Hypothyroidism: 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 Secondary Hypothyroidism
Most recent studies have shown that Secondary Hypothyroidism shares some biological mechanisms with adenoma, adrenal-gland-hypofunction, adrenocorticotropic-hormone-(acth)-deficiency-(disorder), congenital-hypothyroidism, diabetes-mellitus, hyperthyroidism, hypogonadism, hypogonadotropic-hypogonadism, hypopituitarism, hypothyroidism, isolated-thyrotropin-deficiency, neoplasms, pituitary-diseases, pituitary-neoplasms, primary-hypothyroidism, somatotropin-deficiency, thyroid-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Secondary Hypothyroidism, and have been seen in publications frequently: Cell Differentiation, Central Nervous System Development, Cortisol Secretion, Excretion, Gland Development, Glycosylation, Growth Hormone Secretion, Hormone Secretion, Lactation, Localization, Menarche, Menopause, Nervous System Development, Pathogenesis, Pigmentation, Pituitary Gland Development, Reflex, Secretion, System Development, Transport
Quite a number of genes have been found to play important roles in Secondary Hypothyroidism, such as BRD2, CRH, GGH, GH1, GHRH, IGF1, INS, PBX1, PLOD1, POMC, POU1F1, PRL, PROP1, SERPINA7, SLC20A1, SLC25A5, TG, TRH. 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.