C35069Level 8

Thalassemia

**Semantic type:** Disease or Syndrome

**Definition:** An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation.

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C173642Transfusion Dependent Thalassemia

C220180Thalassemia Intermedia

C34368Alpha Thalassemia

C34375Beta Thalassemia

C81288S-Beta Thalassemia

C95538Beta Thalassemia Plus Structural Variants

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