Congenital Defect Of Folate Absorption

Overview of Congenital Defect Of Folate Absorption

Most recent studies have shown that Congenital Defect Of Folate Absorption shares some biological mechanisms with anemia, anemia-macrocytic, anemia-megaloblastic, ataxia, atresia, atrophy, brain-diseases, calcinosis, epilepsy, failure-to-thrive, folic-acid-deficiency, glutamate-formiminotransferase-deficiency, inborn-errors-of-metabolism, malabsorption-syndrome, methylenetetrahydrofolate-reductase-deficiency, neoplasms, nervousness, pancytopenia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Defect Of Folate Absorption, and have been seen in publications frequently: Brain Development, Endocytosis, Folic Acid Transport, Intestinal Absorption, Localization, Myelination, Pathogenesis, Receptor-mediated Endocytosis, Translation, Transport, Tryptophan Transport

Quite a number of genes have been found to play important roles in Congenital Defect Of Folate Absorption, such as B9D1, CSF2, DHFR, EPO, FOLR1, LAMC2, MMAA, MMADHC, MTHFD1, MTHFR, MTR, MTRR, MTX1, NRF1, PRMT1, QDPR, SLC37A1, SLC46A1, THPO. 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.

Congenital Defect Of Folate Absorption Related Genes

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Pathways Related to Congenital Defect Of Folate Absorption

This information is being compiled and will come in a future update

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