| dbo:description
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- Krankheit (de)
- хвороба (uk)
- talasemija, za katero je značilna zmanjšana ali odsotna sinteza globinskih β-verig hemoglobina (sl)
- thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin (en)
- ridotta o assente sintesi delle catene beta dell'emoglobina, ciò può comportare risultati variabili, che vanno da una grave anemia a una condizione clinicamente asintomatica (it)
- talassèmia caracteritzada per una síntesi reduïda o absent de les cadenes d'HBB de l'hemoglobina (ca)
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- Beta-thalassemia genetics, the picture shows one example of how beta-thalassemia is inherited. The beta-globin gene is located on chromosome 11. A child inherits two beta globin genes . (en)
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| dbp:causes
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- Mutations in the HBB gene (en)
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| dbp:diagnosis
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- Blood smear, hemoglobin electrophoresis, iron & ferritin tests, DNA analysis (en)
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| dbp:differential
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- Alpha thalassemia, sickle cell disease, iron deficiency anemia (en)
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- 282.440000 (xsd:double)
- (en)
- D56.1 (en)
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| dbp:prevention
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- Preconception genetic counseling (en)
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| dbp:risks
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- Family history, ancestry from the Mediterranean, West Africa, the Middle East, the Indian subcontinent or Southeast Asia (en)
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| dbp:symptoms
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- Anemia, enlarged spleen, abnormal bone structure (en)
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| dbp:synonyms
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- Cooley's anemia, Mediterranean anemia (en)
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| dbp:treatment
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- Blood transfusion, iron chelation, stem cell transplant, gene therapy (en)
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| dbp:types
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- Beta-thalassemia minor, intermedia and major (en)
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| gold:hypernym
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| rdfs:label
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- Beta thalassemia (en)
- ثلاسيميا بيتا (ar)
- Beta-talassèmia (ca)
- Β-Thalassämie (de)
- Beta-talasemia (es)
- Anemia mediterranea (it)
- Beta-talassemia (pt)
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