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Disease Info Card
Inappropriate Adh Syndrome
Information about Inappropriate Adh Syndrome: 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 Inappropriate Adh Syndrome
Most recent studies have shown that Inappropriate Adh Syndrome shares some biological mechanisms with anti-diuresis-(finding), carcinoma, depressive-disorder, diabetes-mellitus, edema, heart-failure, hyponatraemic, liver-cirrhosis, lung-neoplasms, malignant-neoplasm-of-lung, malignant-neoplasms, neoplasms, nervousness, pituitary-diseases, small-cell-carcinoma-of-lung, water-electrolyte-imbalance, water-intoxication.
Among the many pathways, these few ones have gauged particular interests from scientists studying Inappropriate Adh Syndrome, and have been seen in publications frequently: Aging, Aldosterone Secretion, Coagulation, Diuresis, Excretion, Glomerular Filtration, Hormone Secretion, Localization, Natriuresis, Pathogenesis, Reflex, Renal Sodium Excretion, Renal Water Retention, Secretion, Serotonin Uptake, Transport, Vasoconstriction, Vasopressin Secretion, Water Homeostasis, Water Transport
Quite a number of genes have been found to play important roles in Inappropriate Adh Syndrome, such as ALB, AQP2, AVP, AVPR2, CALCA, CSF2, IFNAR1, IL6, LAMC2, NLRP3, NPPA, OAT, POMC, REN, SLC4A1. 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.