Spherocytosis, Hereditary
"Spherocytosis, Hereditary" 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.
A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
Descriptor ID |
D013103
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MeSH Number(s) |
C15.378.071.141.150.785 C16.320.070.785
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Spherocytosis, Hereditary".
- 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]
- Spherocytosis, Hereditary [C15.378.071.141.150.785]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Spherocytosis, Hereditary [C16.320.070.785]
Below are MeSH descriptors whose meaning is more specific than "Spherocytosis, Hereditary".
This graph shows the total number of publications written about "Spherocytosis, Hereditary" by people in this website by year, and whether "Spherocytosis, Hereditary" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2009 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spherocytosis, Hereditary" by people in Profiles.
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Abdullah F, Zhang Y, Camp M, Rossberg MI, Bathurst MA, Colombani PM, Casella JF, Nabaweesi R, Chang DC. Splenectomy in hereditary spherocytosis: Review of 1,657 patients and application of the pediatric quality indicators. Pediatr Blood Cancer. 2009 Jul; 52(7):834-7.
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Kwiatkowska J. [Erythrocyte metabolism in hereditary spherocytosis]. Acta Haematol Pol. 1971 Apr-Jun; 2(2):187-93.