Disease Info Card

Hereditary Spherocytosis

Information about Hereditary Spherocytosis: 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 Hereditary Spherocytosis

Most recent studies have shown that Hereditary Spherocytosis shares some biological mechanisms with anemia, anemia-hemolytic, anemia-hemolytic-congenital, anemia-sickle-cell, aplastic-anemia, autoimmune-hemolytic-anemia, autoimmune-reaction, beta-thalassemia, cholelithiasis, elliptocytosis-hereditary, glucosephosphate-dehydrogenase-deficiency, hematological-disease, hemolysis-(disorder), hemorrhage, hyperbilirubinemia, icterus, purpura, purpura-thrombocytopenic-idiopathic, thalassemia, thrombocytopenic-purpura.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Spherocytosis, and have been seen in publications frequently: Aging, Anion Transport, Cation Transport, Cell Adhesion, Coagulation, Excretion, Gallstone Formation, Glycolysis, Hemopoiesis, Hemostasis, Localization, Methylation, Pathogenesis, Phagocytosis, Protein Phosphorylation, Proteolysis, Regeneration, Senescence, Translation, Transport

Quite a number of genes have been found to play important roles in Hereditary Spherocytosis, such as ACHE, ANK1, EPB41, EPB41L1, EPB42, EPO, ETFA, G6PD, HP, MAP3K14, MUC1, SLC4A1, SPTA1, SPTB, TF. 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.