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Disease Info Card
Congenital Methemoglobinemia
Information about Congenital Methemoglobinemia: 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 Methemoglobinemia
Most recent studies have shown that Congenital Methemoglobinemia shares some biological mechanisms with acquired-methemoglobinemia, anemia-hemolytic, anoxia, athetosis, cerebral-palsy, congenital-heart-defects, cyanosis, foramen-ovale-patent, heart-diseases, hemoglobinopathies, inborn-errors-of-metabolism, malignant-neoplasms, metabolic-diseases, methemoglobin-reductase-deficiency, methemoglobinemia, nadh-cytochrome-b5-reductase-deficiency, severe-mental-retardation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Methemoglobinemia, and have been seen in publications frequently: Cell Growth, Formate Oxidation, Glycolysis, Localization, Pathogenesis, Proteolysis, Rna Interference, Translation
Quite a number of genes have been found to play important roles in Congenital Methemoglobinemia, such as ATAT1, BRCA2, CYB5A, CYB5R3, DIAPH1, DIAPH2, DLD, FANCD2, G6PD, GSR, GSTK1, HBB, HBG2, LIF, MB, PSEN1, TGM2, 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.
Pathways Related to Congenital Methemoglobinemia
This information is being compiled and will come in a future update
| Cell Growth | Formate Oxidation | Glycolysis |
| Localization | Pathogenesis | Proteolysis |
| Rna Interference | Translation |