Beta-thalassemia intermedia

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Beta-thalassemia intermedia

ORPHA:231222Disease

Also called Beta-NTDT · Non-transfusion dependent beta-thalassemia

What it is

Beta-thalassemia (BT) intermedia is a form of BT characterized by mild to moderate anemia which does not or only occasionally requires transfusion.

Key facts

Age of onset
Childhood
Inheritance
Autosomal recessive
Classified as
Disease

Recorded for the broader condition

Prevalence
1-9 / 1 000 000 (France)Beta-thalassemia

Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Gene

HBBDisease-causing germline mutation(s)

ICD-10 codes

D56.1filed under a broader ICD-10 category — shared with 5 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MEDDRA 10062923MONDO 0016487OMIM 613985UMLS C0472767

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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