Alport Syndrome, X-linked

Overview of Alport Syndrome, X-linked

Most recent studies have shown that Alport Syndrome, X-linked shares some biological mechanisms with benign-familial-haematuria, complete-hearing-loss, esophageal-neoplasms, familial-hematuria, genetic-diseases-x-linked, glioblastoma, glomerulonephritis, hereditary-diseases, hereditary-nephritis, kidney-diseases, kidney-failure, kidney-failure-chronic, leiomyomatosis, membranous-glomerulonephritis, nephritis, proteinuria-of-undiagnosed-cause, retinal-diseases, sensorineural-hearing-loss-(disorder), thin-basement-membrane-disease.

Among the many pathways, these few ones have gauged particular interests from scientists studying Alport Syndrome, X-linked, and have been seen in publications frequently: Cell Differentiation, Cell Proliferation, Excretion, Glomerular Filtration, Localization, Mrna Splicing, Pathogenesis, Pigmentation, Reflex, Reverse Transcription, Rna Processing, Sex Determination, Translation

Quite a number of genes have been found to play important roles in Alport Syndrome, X-linked, such as AR, CLU, COL4A1, COL4A3, COL4A4, COL4A5, COL4A6, CTSG, DCX, EDAR, FDXR, GAPDH, MMP14, MMP2, MMP9, SLC2A10, STS. 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.

Alport Syndrome, X-linked Related Genes

click to see detail information for each gene

Pathways Related to Alport Syndrome, X-linked

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

Related Diseases