 Anemia, Hemolytic, Congenital Nonspherocytic
"Anemia, Hemolytic, Congenital Nonspherocytic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D000746
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| MeSH Number(s) |
C15.378.071.141.150.100 C16.320.070.100
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| Concept/Terms |
Anemia, Hemolytic, Congenital Nonspherocytic- Anemia, Hemolytic, Congenital Nonspherocytic
- Anemia, Hemolytic Congenital, Nonspherocytic
- Hemolytic Anemia, Congenital Nonspherocytic
- Anemia, Congenital Nonspherocytic Hemolytic
- Congenital Nonspherocytic Hemolytic Anemia
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Below are MeSH descriptors whose meaning is more general than "Anemia, Hemolytic, Congenital Nonspherocytic".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Anemia, Hemolytic, Congenital Nonspherocytic [C15.378.071.141.150.100]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Anemia, Hemolytic, Congenital Nonspherocytic [C16.320.070.100]
Below are MeSH descriptors whose meaning is more specific than "Anemia, Hemolytic, Congenital Nonspherocytic".
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