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Items: 3

1.

Hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain

MedGen UID:
333610
Concept ID:
C1840647
Disease or Syndrome
2.

Compensated hemolytic anemia

MedGen UID:
870825
Concept ID:
C4025283
Disease or Syndrome
3.

Gluthathione peroxidase deficiency

Several documented cases of glutathione peroxidase (GPX1; 138320) deficiency in association with hemolytic anemia have been reported. However, Paglia (1989) stated: 'To date, no defects in glutathione peroxidase have been unequivocally incriminated in the pathogenesis of hemolytic syndromes, although several instances of partial deficiency have been reported in patients with anemias of unknown etiology. This association may be coincidental, since there is a broad range of ethnic variation in the erythrocyte enzyme' (Beutler and Matsumoto, 1975). [from OMIM]

MedGen UID:
473098
Concept ID:
C0398747
Disease or Syndrome
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