Disease

Hereditary Folate Malabsorption

About the Disease
Folate Malabsorption, Hereditary, also known as hereditary folate malabsorption, is related to megaloblastic anemia and deficiency anemia, and has symptoms including ataxia, athetosis and diarrhea. An important gene associated with Folate Malabsorption, Hereditary is SLC46A1 (Solute Carrier Family 46 Member 1), and among its related pathways/superpathways are Metabolism and Metabolism of water-soluble vitamins and cofactors. Affiliated tissues include brain, skin and skeletal muscle, and related phenotypes are failure to thrive and nausea and vomiting

Common Targets
SLC46A1

疾病靶点研报
Hereditary Folate Malabsorption

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