has material basis in germline mutation in PGK1 disorder of glycogen metabolism hemolytic anemia glycogen storage disease due to phosphoglycerate kinase 1 deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/phosphoglycerate_kinase_1_deficiency MONDO:0010392 glycogenosis due to phosphoglycerate kinase 1 deficiency UMLS:C1970848 Phosphoglycerate kinase (PGK) deficiency is a metabolic disorder characterized by variable combinations of nonspherocytic hemolytic anemia, myopathy, and various central nervous system abnormalities. Phosphoglycerate Kinase Deficiency GARD:0007389 glycogen storage disease caused by mutation in PGK1 Orphanet:713 icd11.foundation:1396572570 NANDO:1200831 glycogen storage disease due to phosphoglycerate kinase 1 deficiency NCIT:C126738 OMIM:300653 PGK1 glycogen storage disease DOID:0111933 MESH:C567067 Phosphoglycerate kinase deficiency NORD:1577 GSD due to phosphoglycerate kinase 1 deficiency PGK deficiency MEDGEN:410166 phosphoglycerate kinase 1 deficiency, X-linked recessive obsolete muscular glycogenosis disorder of glycolysis anemia due to erythrocyte enzyme disorder