Elliptocytosis, Hereditary
"Elliptocytosis, 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.
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
| Descriptor ID |
D004612
|
| MeSH Number(s) |
C15.378.071.141.150.365 C16.320.070.365
|
| Concept/Terms |
Elliptocytosis, Hereditary- Elliptocytosis, Hereditary
- Elliptocytoses, Hereditary
- Hereditary Elliptocytoses
- Hereditary Elliptocytosis
- Ovalocytosis, Hereditary
- Hereditary Ovalocytoses
- Hereditary Ovalocytosis
- Ovalocytoses, Hereditary
|
Below are MeSH descriptors whose meaning is more general than "Elliptocytosis, 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]
- Elliptocytosis, Hereditary [C15.378.071.141.150.365]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Elliptocytosis, Hereditary [C16.320.070.365]
Below are MeSH descriptors whose meaning is more specific than "Elliptocytosis, Hereditary".
This graph shows the total number of publications written about "Elliptocytosis, Hereditary" by people in this website by year, and whether "Elliptocytosis, Hereditary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Elliptocytosis, Hereditary" by people in Profiles.
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Risinger M, Christakopoulos GE, Schultz CL, McGann PT, Zhang W, Kalfa TA. Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity. Pediatr Blood Cancer. 2019 02; 66(2):e27531.