has material basis in germline mutation in ALDOA disorder of glycogen metabolism familial hemolytic anemia glycogen storage disease due to aldolase A deficiency https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/glycogen_storage_disease_xii OMIM:611881 glycogen storage disease XII NANDO:1200834 GSD due to aldolase A deficiency glycogen storage disease type XII glycogen storage disease due to aldolase A deficiency glycogen storage disease type 12 glycogen storage disease 12 MESH:C562718 UMLS:C0272066 Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggered by fever) without hemolytic anemia has recently been reported. MEDGEN:82895 glycogenosis type XII MONDO:0012747 glycogenosis type 12 GARD:0000600 glycogenosis due to aldolase A deficiency SCTID:111578003 ICD9:282.3 GSD type XII icd11.foundation:1020924235 GSD type 12 GSD12 Orphanet:57 aldolase deficiency red cell disorder of glycolysis anemia due to erythrocyte enzyme disorder