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Disease Info Card
Hypocalcemic Tetany
Information about Hypocalcemic Tetany: 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 Hypocalcemic Tetany
Most recent studies have shown that Hypocalcemic Tetany shares some biological mechanisms with adenoma, bone-diseases, digeorge-syndrome, dog-diseases, dwarfism, hypercalcemia, hyperparathyroidism-primary, hyperphosphatemia, hypocalcemia, hypoparathyroidism, infective-disorder, kidney-failure, late-neonatal-hypocalcemia, pregnancy-complications, pseudohypoparathyroidism, rickets, tetany, vitamin-d-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypocalcemic Tetany, and have been seen in publications frequently: Anaphylaxis, Bone Mineralization, Bone Resorption, Calcitonin Secretion, Endocytosis, Excretion, Growth Hormone Secretion, Hatching, Hormone Secretion, Intestinal Absorption, Localization, Methylation, Pathogenesis, Secretion, Transport, Vasodilation
Quite a number of genes have been found to play important roles in Hypocalcemic Tetany, such as ALB, ALPP, ASRGL1, ATRNL1, CALCA, CCL27, CLDN16, CSF2, ENO2, GNAS, LAMC2, NAT10, PDLIM3, PTH, PTRH1, SH3D19, SLPI. 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.