Belgian Genetic Tests database
Hemoglobin H disease
| Name: |
Hemoglobin H disease
|
| Description: |
An intermediate form of alpha-thalassemia characterized by increased hemolysis and mild to severe anemia with marked microcytosis and hypochromia. Hemoglobin H disease (HbH) disease belongs to the group of nontransfusion-dependent thalassemia.
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| ORPHAcode: |
93616
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| Synonyms: |
Alpha-thalassemia intermedia
HbH disease
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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