 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
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| 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".
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