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Disease Info Card
11-beta-hydroxylase Deficiency
Information about 11-beta-hydroxylase 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 11-beta-hydroxylase Deficiency
Most recent studies have shown that 11-beta-hydroxylase Deficiency shares some biological mechanisms with 17-alpha-hydroxylase-deficiency, 3-beta-hydroxysteroid-dehydrogenase-deficiency, adenoma, adrenal-gland-hypofunction, adrenal-hyperplasia, adrenogenital-syndrome, ambiguous-genitalia, chronic-active-hepatitis, congenital-adrenal-hyperplasia, cushing-syndrome, gynecomastia, hyperaldosteronism, hyperplasia, hypertensive-disease, neoplasms, precocious-puberty, virilism.
Among the many pathways, these few ones have gauged particular interests from scientists studying 11-beta-hydroxylase Deficiency, and have been seen in publications frequently: Aldosterone Secretion, Androgen Secretion, Bone Maturation, Cortisol Secretion, Excretion, Fertilization, Gene Conversion, Hormone Secretion, Ion Transport, Menarche, Metaphase, Pathogenesis, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in 11-beta-hydroxylase Deficiency, such as AGT, APCDD1, BRD2, CA2, CYP11B1, CYP11B2, CYP17A1, CYP21A2, DLL4, PLOD1, POMC, PPA1, PRL, REN, S100A6, SHBG, SLC25A20, TH. 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.