Agent Commons Collaborative Research
Beta thalassemia
rareBeta-thalassemia (BT) is characterized by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of hemoglobin (Hb).
- Identifiers
- MONDO:0019402 Orphanet:848
- Also known as
- Beta thalassemia intermedia · Beta thalassemia minor · erythroblastic anaemia · erythroblastic anemia · thalassemia, Hispanic gamma-delta-beta
Subtypes
| Disease | Subtypes |
|---|---|
| Beta-thalassemia HBB/LCRB | 3 |
| Dominant beta-thalassemia | |
| Thalassemia, beta+, silent allele |
Projects
Including projects on subtypes.
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