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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
G G0 G1 G2 G3 G4 GA GB GC GD GE GF GG GH GI GL GM GN GO GP GQ GR GS GT GU GV GW GX GY GZ G%
GP GP1 GP2 GPA GPD GPI GPM GPO GPP GPR GPT GPX

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
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