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Disease Info Card
Hydrops Fetalis
Information about Hydrops Fetalis: 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 Hydrops Fetalis
Most recent studies have shown that Hydrops Fetalis shares some biological mechanisms with alpha-thalassemia, anemia, congenital-abnormality, disease-due-to-parvoviridae, edema, erythema-infectiosum, erythroblastosis-fetal, fetal-death, fetal-diseases, heart-failure, hydrops-fetalis-non-immune, neoplasms, parvovirus-b19-(disease), pleural-effusion-disorder, polyhydramnios, pregnancy-complications, pregnancy-complications-infectious, thalassemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hydrops Fetalis, and have been seen in publications frequently: Angiogenesis, Cell Proliferation, Coagulation, Dna Amplification, Excretion, Fertilization, Glycosylation, Immune Response, Interphase, Localization, Lung Development, Lung Growth, Ossification, Parturition, Pathogenesis, Sensitization, Transport, Transposition, Tropism, Urea Cycle
Quite a number of genes have been found to play important roles in Hydrops Fetalis, such as ABO, AFP, ALB, CALR, CS, EVA1C, FLT4, GBA, GLB1, GUSB, HBA1, HBZ, HUNK, PTPN11, RHCE, RHD, SSB. 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.