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Disease Info Card
Hemolytic Disorder
Information about Hemolytic Disorder: 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 Hemolytic Disorder
Most recent studies have shown that Hemolytic Disorder shares some biological mechanisms with abo-haemolytic-disease-of-newborn, alloimmunization, anemia, anemia-hemolytic, autoimmune-hemolytic-anemia, autoimmune-reaction, blood-group-incompatibility, edema, erythroblastosis-fetal, fetal-death, fetal-diseases, hemolysis-(disorder), hemorrhage, hyperbilirubinemia, icterus, neonatal-jaundice, pregnancy-complications-hematologic, rh-isoimmunization, rheumatic-heart-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hemolytic Disorder, and have been seen in publications frequently: Anaphylaxis, Antibody-dependent Cellular Cytotoxicity, Coagulation, Complement Activation, Conjugation, Excretion, Fertilization, Glycosylation, Immune Response, Lactation, Parturition, Pathogenesis, Phagocytosis, Pigmentation, Proteolysis, Respiratory Burst, Secretion, Sensitization, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Hemolytic Disorder, such as ABO, ACHE, ALB, CD55, EPO, FUZ, G6PD, GYPA, IGHG3, POMC, RHCE, RHD, RHO, RHOD, SLC6A3, UBL4A. 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.