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Disease Info Card
Idiopathic Growth Hormone Deficiency
Information about Idiopathic Growth 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 Idiopathic Growth Hormone Deficiency
Most recent studies have shown that Idiopathic Growth Hormone Deficiency shares some biological mechanisms with craniopharyngioma, dwarfism, growth-disorders, hypopituitarism, hypoplasia, hypothyroidism, isolated-somatotropin-deficiency, malnutrition, neoplasms, pituitary-diseases, pituitary-dwarfism, pituitary-neoplasms, positions-of-breech-presentation, shwachman-syndrome, somatotropin-deficiency, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Idiopathic Growth Hormone Deficiency, and have been seen in publications frequently: Bone Mineralization, Bone Resorption, Development Of Secondary Sexual Characteristics, Gene Conversion, Growth Hormone Secretion, Hormone Secretion, Pathogenesis, Regeneration, Secondary Growth, Secretion, Thelarche
Quite a number of genes have been found to play important roles in Idiopathic Growth Hormone Deficiency, such as CACNA1C, ERMAP, GGH, GH1, GHRH, IGF1, IGF2, IGHD, INS, POMC, POU1F1, RANGAP1, SERPINA7, SHBG, SLC17A5, SLC20A1, TBXAS1, TYMS. 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.