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Hemolytic anemia due to hexokinase deficiency

MedGen UID:
461693
Concept ID:
C3150343
Disease or Syndrome
Synonyms: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY; Hexokinase deficiency hemolytic anemia
 
Gene (location): HK1 (10q22.1)
OMIM®: 235700

Definition

Hexokinase deficiency is an autosomal recessive disorder characterized by early-onset severe hemolytic anemia (summary by van Wijk et al., 2003). [from OMIM]

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