G6PD deficiency
[common hereditary enzyme deficiency causing varying degrees of hemolytic anemia; can cause favism, some drug induced hemolytic anemias, and chronic nonspherocytic hemolytic anemia. ( CSP )]
UMLS (CSP) C0017920- Disease or Syndrome
Relation/PAR: ANEMIA HEMOLITIKOA
glycogen storage disease
Congenital Metabolic Disorder
enzyme deficiency
glycogen storage disease
Congenital Metabolic Disorder
enzyme deficiency
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