Disease Info Card

Congenital Absence Of Kidney

Information about Congenital Absence Of Kidney: 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 Congenital Absence Of Kidney

Most recent studies have shown that Congenital Absence Of Kidney shares some biological mechanisms with anus-imperforate, atresia, congenital-abnormality, congenital-absence, congenital-duplication-of-uterus, dysplasia, fetal-diseases, gastroesophageal-reflux-disease, genital-diseases-male, hydronephrosis, hypoplasia, kidney-diseases, multicystic-dysplastic-kidney, neoplasms, oligohydramnios, pain, polycystic-kidney-diseases, renal-dysplasia, unilateral-agenesis-of-kidney, urogenital-abnormalities.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Absence Of Kidney, and have been seen in publications frequently: Cell Adhesion, Diuresis, Enucleation, Excretion, Fertilization, Glomerular Filtration, Kidney Development, Localization, Lung Development, Lung Growth, Menarche, Menstruation, Micturition, Ossification, Pathogenesis, Secretion, Segmentation, Spermatogenesis, Transposition, Ureter Maturation

Quite a number of genes have been found to play important roles in Congenital Absence Of Kidney, such as ACE, AFP, AGT, BMP4, CFTR, COL18A1, EYA1, FRAS1, FREM1, FREM2, GDNF, OXSM, PAX2, RAPGEF5, RET, STS, WT1. 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.