Disease Info Card

Familial Hematuria

Information about Familial Hematuria: 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 Familial Hematuria

Most recent studies have shown that Familial Hematuria shares some biological mechanisms with alport-syndrome-x-linked, benign-familial-haematuria, complete-hearing-loss, focal-glomerulosclerosis, glioblastoma, glomerulonephritis, glomerulosclerosis-(disorder), hereditary-nephritis, hypertensive-disease, iga-glomerulonephritis, kidney-diseases, kidney-failure, kidney-failure-chronic, microscopic-hematuria, nephritis, proteinuria-of-undiagnosed-cause, sclerosis, segmental-glomerulosclerosis, sensorineural-hearing-loss-(disorder), thin-basement-membrane-disease.

Among the many pathways, these few ones have gauged particular interests from scientists studying Familial Hematuria, and have been seen in publications frequently: Angiogenesis, Complement Activation, Glomerular Filtration, Pathogenesis, Segmentation

Quite a number of genes have been found to play important roles in Familial Hematuria, such as ABO, C1QL1, C3, CFHR5, COL4A3, COL4A4, COL4A5, CRH, FBLN1, FMN1, GLA, LYZ, MB, NEFH, NOTCH4, PLP2, PPP1R1A, SGCG, SLC2A10, SQLE. 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.