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Disease Info Card
Infantile Hypophosphatasia
Information about Infantile Hypophosphatasia: 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 Infantile Hypophosphatasia
Most recent studies have shown that Infantile Hypophosphatasia shares some biological mechanisms with bone-diseases, congenital-abnormality, craniosynostosis, dwarfism, epilepsy, familial-hypophosphatemia, fetal-diseases, fracture, hereditary-pyropoikilocytosis, hypercalcemia, hypophosphatasia, inborn-errors-of-metabolism, metabolic-bone-disorder, nephrocalcinosis, osteomalacia, osteopenia, rickets.
Among the many pathways, these few ones have gauged particular interests from scientists studying Infantile Hypophosphatasia, and have been seen in publications frequently: Bone Maturation, Bone Mineralization, Bone Resorption, Cell Growth, Cell Proliferation, Chondrocyte Differentiation, Contact Inhibition, Dentin Mineralization, Excretion, Glycosylation, Localization, Odontogenesis, Ossification, Regulation Of Cell Growth, Root Development
Quite a number of genes have been found to play important roles in Infantile Hypophosphatasia, such as ALPL, ALPP, ASRGL1, ATRNL1, CALCA, CCL27, LAMC2, NAT10, PDLIM3, PDXP, PLP1, PRDX5, PTH, PTHLH, RUNX2, SLPI, SPP1, TMUB1. 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.