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Disease Info Card
Isolated Adrenocorticotropic Hormone Deficiency
Information about Isolated Adrenocorticotropic Hormone Deficiency: 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 Isolated Adrenocorticotropic Hormone Deficiency
Most recent studies have shown that Isolated Adrenocorticotropic Hormone Deficiency shares some biological mechanisms with addison-disease, adrenal-gland-hypofunction, adrenocorticotropic-hormone-(acth)-deficiency-(disorder), autoimmune-diseases, autoimmune-reaction, comatose, cushing-syndrome, diabetes-mellitus, empty-sella-syndrome, hashimoto-disease, hypoglycemia, hypopituitarism, hypotension-adverse-event, hypothyroidism, pituitary-diseases, primary-hypothyroidism, secondary-adrenocortical-insufficiency, thyroiditis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Isolated Adrenocorticotropic Hormone Deficiency, and have been seen in publications frequently: Circadian Rhythm, Coagulation, Cortisol Secretion, Diuresis, Excretion, Glomerular Filtration, Gluconeogenesis, Hormone Secretion, Hormone Transport, Menstruation, Mrna Splicing, Muscle Atrophy, Natriuresis, Pathogenesis, Pigmentation, Prolactin Secretion, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Isolated Adrenocorticotropic Hormone Deficiency, such as AVP, BRD2, C1QL1, CRH, GCG, GGH, GH1, GHRH, GNRH1, INS, PBX1, PITX1, PLOD1, POMC, PRL, REN, TBX19, 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.