Disease Info Card

Erythroblastosis, Fetal

Information about Erythroblastosis, Fetal: 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 Erythroblastosis, Fetal

Most recent studies have shown that Erythroblastosis, Fetal shares some biological mechanisms with alloimmunization, anemia, anemia-hemolytic, blood-group-incompatibility, edema, erythroblastosis, fetal-death, fetal-diseases, fetomaternal-transfusion, hemolysis-(disorder), hemolytic-disorder, hyperbilirubinemia, icterus, kernicterus, neonatal-jaundice, pre-eclampsia, pregnancy-complications, pregnancy-complications-hematologic, rh-incompatibility, rh-isoimmunization.

Among the many pathways, these few ones have gauged particular interests from scientists studying Erythroblastosis, Fetal, and have been seen in publications frequently: Bilirubin Conjugation, Blood Coagulation, Coagulation, Conjugation, Excretion, Fertilization, Fibrinolysis, Glycosylation, Immune Response, Localization, Opsonization, Parturition, Pathogenesis, Phagocytosis, Pigmentation, Regeneration, Secretion, Sensitization, Sex Determination, Transport

Quite a number of genes have been found to play important roles in Erythroblastosis, Fetal, such as ABO, ACHE, ALB, CSH1, CSH2, EPO, G6PD, GYPA, IGHG3, INS, POMC, RHCE, RHD, RHO, RHOD, SLC6A3, TNFSF14. 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.