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Hemoglobin E-beta-thalassemia syndrome
rareHemoglobin E - beta-thalassemia (HbE - BT) is a form of beta-thalassemia that results in a mild to severe clinical presentation ranging from a condition indistinguishable from beta-thalassemia major to a mild form of beta-thalassemia intermedia.
- Identifiers
- MONDO:0016491 Orphanet:231249
- Also known as
- E-beta-thalassemia · HbE-beta-thalassemia syndrome
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