hemoglobin H disease (Q3144945)
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alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
- HBH
- alpha thalassemia, hemoglobin H type
- alpha-thalassemia intermedia
- hemoglobin H disease, deletional
- Hemoglobin H disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hemoglobin H disease |
alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other |
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Statements
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Identifiers
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Sitelinks
Wikipedia(3 entries)
- arwiki داء الهيموغلوبين H
- enwiki Hemoglobin H disease
- frwiki Hémoglobinose H