Pyruvate Kinase Deficiency of Red Cells

An autosomal recessive metabolic disorder caused by mutations in the PKLR gene (pyruvate kinase). It is the most common cause of hereditary nonspherocytic hemolytic anemia and is also the most frequent enzyme abnormality of GLYCOLYSIS. OMIM: 266200

Also Known As:

PK Deficiency; Pyruvate Kinase Deficiency; Pyruvate Kinase Deficiency of Erythrocyte

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Anemia: 39278
    - Hemolytic Anemia: 6775
      - Congenital Hemolytic Anemia: 292
        Congenital Nonspherocytic Hemolytic Anemia: 42
        Pyruvate Kinase Deficiency of Red Cells: 371
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inborn Errors Metabolism: 1183
    - Inborn Errors Carbohydrate Metabolism
      - Inborn Errors Pyruvate Metabolism
        Pyruvate Kinase Deficiency of Red Cells: 371
  - Congenital Hemolytic Anemia: 292
    - Congenital Nonspherocytic Hemolytic Anemia: 42
      - Pyruvate Kinase Deficiency of Red Cells: 371
Enzymes and Coenzymes: 1
- Enzymes: 155591
  - Transferases: 6719
    - Phosphotransferases: 43773
      - Phosphotransferases (Alcohol Group Acceptor)
        Pyruvate Kinase: 1875
        Pyruvate Kinase Deficiency of Red Cells: 371
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - Inborn Errors Metabolism: 1183
    - Inborn Errors Carbohydrate Metabolism
      - Inborn Errors Pyruvate Metabolism
        Pyruvate Kinase Deficiency of Red Cells: 371

Maria Del Mar Mañu-Pereira Selected Research

Maria Del Mar Mañu-Pereira Research Topics

Disease

Drug/Important Bio-Agent (IBA)