Congenital Abnormality Of The Urinary System

Overview of Congenital Abnormality Of The Urinary System

Most recent studies have shown that Congenital Abnormality Of The Urinary System shares some biological mechanisms with congenital-abnormality, congenital-absence-of-kidney, diabetes-mellitus, dysplasia, fetal-diseases, gastroesophageal-reflux-disease, hydronephrosis, infection-of-kidney, infective-disorder, kidney-diseases, kidney-failure, kidney-failure-chronic, neoplasms, proteinuria-of-undiagnosed-cause, ureteral-obstruction, ureterocele, urinary-tract-infection, urogenital-abnormalities, urologic-diseases, vesico-ureteral-reflux.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Abnormality Of The Urinary System, and have been seen in publications frequently: Anaphylaxis, Cell Proliferation, Diuresis, Excretion, Lipoprotein Oxidation, Oxalate Transport, Pathogenesis, Reflex, Segmentation, Transport, Ureter Maturation

Quite a number of genes have been found to play important roles in Congenital Abnormality Of The Urinary System, such as ABO, ACE, AMBP, AVP, BMP4, C1QL1, CCNB1, CRH, CUBN, CUTA, HNF1B, ID2, INVS, PTCH1, RAPGEF5, RHD, SHH, SMOX. 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.

Congenital Abnormality Of The Urinary System Related Genes

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Pathways Related to Congenital Abnormality Of The Urinary System

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

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