Phosphoglycerate Kinase 1 Deficiency (PGK1D)

Phosphoglycerate Kinase 1 Deficiency, also known as glycogen storage disease due to phosphoglycerate kinase 1 deficiency, is related to congenital nonspherocytic hemolytic anemia and hemolytic anemia, and has symptoms including ataxia and seizures. An important gene associated with Phosphoglycerate Kinase 1 Deficiency is PGK1 (Phosphoglycerate Kinase 1), and among its related pathways/superpathways are glycolysis (BioCyc) and Glycolysis (REACTOME). The drug Pharmaceutical Solutions has been mentioned in the context of this disorder. Affiliated tissues include kidney and skin, and related phenotypes are intellectual disability and ataxia