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hemoglobin E-beta-thalassemia syndrome

MONDO:0016491

Also known as: E-beta-thalassemia, HbE-beta-thalassemia syndrome

MONDO:
MONDO:0016491
Orphanet:
231249
Rare disease52 associated genes

Description

Hemoglobin 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.

Associated genes

+42 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.