Alpha thalassemia is a genetic blood disorder characterized by reduced production of hemoglobin due to mutations in the alpha-globin genes. This condition can lead to varying degrees of anemia, requiring careful diagnosis and management. The ICD-10 Code D56.0 facilitates accurate documentation, billing, and public health reporting, ensuring that healthcare providers can effectively track and manage this condition.
ICD-10 Code D56.0 specifically denotes Alpha thalassemia, a hereditary condition that results in decreased synthesis of alpha-globin chains, leading to imbalanced hemoglobin production. This code should be utilized in clinical documentation and billing when diagnosing patients with this condition, particularly when assessing the severity of anemia and planning appropriate treatment.
Alpha thalassemia is caused by genetic mutations affecting the alpha-globin genes, leading to insufficient hemoglobin production. The condition can progress to varying degrees of anemia, necessitating medical intervention to manage symptoms and prevent complications. Early diagnosis is crucial for effective treatment.
In SOAP notes, ICD-10 Code D56.0 is essential for documenting the patient's symptoms, assessment findings, and treatment plans related to Alpha thalassemia. This code is relevant in both acute and chronic care settings, ensuring comprehensive patient management.
ICD-10 Code D56.0 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Alpha thalassemia. This code is vital for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Alpha thalassemia may require hospitalization for severe cases, particularly when complications arise. Treatment focuses on managing symptoms and preventing complications.


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Learn moreICD-10 Code D56.0 is critical for billing purposes in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 36430 | Transfusion of blood products. |
| 85025 | Complete blood count (CBC) with automated differential. |
| 96372 | Therapeutic, prophylactic, or diagnostic injection. |
Common Questions About Using ICD-10 Code D56.0 for Alpha thalassemia
What are the common symptoms of Alpha thalassemia?
Common symptoms include fatigue, weakness, pallor, and shortness of breath. Patients may also experience splenomegaly and have a family history of the condition.
How is Alpha thalassemia diagnosed?
Diagnosis is typically made through blood tests that measure hemoglobin levels and genetic testing to identify mutations in the alpha-globin genes.
What treatments are available for Alpha thalassemia?
Treatment options include regular blood transfusions, iron chelation therapy, and supportive care to manage symptoms and prevent complications.
Is Alpha thalassemia a contagious disease?
No, Alpha thalassemia is a genetic disorder and is not contagious. It is inherited from parents who carry the gene mutations.
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