"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 familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
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 the URMC Research Network by year, and whether "Spherocytosis, Hereditary" was a major or minor topic of these publication.