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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

Preferred term

Anemia, Hemolytic, Congenital Nonspherocytic  

Type

  • Topical Descriptor

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Related concepts

Entry terms

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

Scope note

  • 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.

History note

  • 91(82)68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67

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URI

http://www.yso.fi/onto/mesh/D000746

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