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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Anemia, Hemolytic, Congenital Nonspherocytic
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Anemia, Hemolytic, Congenital Nonspherocytic

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Anemia, Hemolytic, Congenital Nonspherocytic  

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Tipo

  • mesh:Descriptor

Definición

  • Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Anemia, Congenital Nonspherocytic Hemolytic
  • Anemia, Hemolytic Congenital, Nonspherocytic
  • Congenital Nonspherocytic Hemolytic Anemia
  • Hemolytic Anemia, Congenital Nonspherocytic

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-GVX77QM2-G

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