Anemia, Hemolytic, Congenital Nonspherocytic

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.

Year introduced: 1991(1982)1968

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Tree Number(s): C15.378.050.141.150.100, C16.320.070.100

MeSH Unique ID: D000746

Entry Terms:

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

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic