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
|
| MeSH Number(s) |
C15.378.071.141.150.100 C16.320.070.100
|
| 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
|
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".
This graph shows the total number of publications written about "Anemia, Hemolytic, Congenital Nonspherocytic" by people in this website by year, and whether "Anemia, Hemolytic, Congenital Nonspherocytic" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Anemia, Hemolytic, Congenital Nonspherocytic" by people in Profiles.
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Diagnosis, monitoring, and management of pyruvate kinase deficiency in children. Pediatr Blood Cancer. 2022 08; 69(8):e29696.
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Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency. Am J Hematol. 2020 05; 95(5):472-482.
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Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study. Blood. 2018 05 17; 131(20):2183-2192.
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Study of the molecular defects in pyruvate kinase deficient patients affected by nonspherocytic hemolytic anemia. Blood Cells Mol Dis. 1995; 21(1):49-55.