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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Glucosephosphate Dehydrogenase Deficiency
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Glucosephosphate Dehydrogenase Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Glucosephosphate Dehydrogenase Deficiency
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Glucosephosphate Dehydrogenase Deficiency

Preferred term

Glucosephosphate Dehydrogenase Deficiency  

Type

  • mesh:Descriptor

Definition

  • A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.

Broader concept

Narrower concepts

Entry terms

  • Deficiency, Glucosephosphate Dehydrogenase
  • Deficiency, GPD
  • Deficiency of Glucose-6-Phosphate Dehydrogenase
  • G6PD Deficiency
  • Glucose 6 Phosphate Dehydrogenase Deficiency
  • Glucose-6-Phosphate Dehydrogenase Deficiency
  • Glucosephosphate Dehydrogenase Deficiencies
  • GPD Deficiency
  • Hemolytic Anemia Due to G6PD Deficiency

Allowable Qualifier(s)

In other languages

URI

http://data.loterre.fr/ark:/67375/JVR-PT2GC7RZ-R

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