Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

Overview of Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

Most recent studies have shown that Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets shares some biological mechanisms with autosomal-dominant-hypophosphatemic-rickets, bone-demineralization-pathologic, bone-diseases, cardiovascular-diseases, congenital-abnormality, familial-hypophosphatemia, familial-hypophosphatemic-bone-disease, growth-retardation, hypercalciuria, hypophosphatemia, hypophosphatemic-rickets, kidney-diseases, kidney-failure-chronic, liver-diseases, malabsorption-syndrome, metabolic-bone-disorder, oncogenic-osteomalacia, osteomalacia, rickets.

Among the many pathways, these few ones have gauged particular interests from scientists studying Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets, and have been seen in publications frequently: Bone Mineralization, Dentinogenesis, Excretion, Mrna Splicing, Pathogenesis, Renal Phosphate Excretion, Secretion, Secretory Pathway

Quite a number of genes have been found to play important roles in Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets, such as AVPR2, BGLAP, CYP24A1, DMP1, DMTF1, ENPP1, FGF23, GSTP1, IBSP, MEPE, PHEX, PTH, RAPGEF5, SERPINA1, SLC17A2, SLC34A1. 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.

Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets Related Genes

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Pathways Related to Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

This information is being compiled and will come in a future update

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