Beta thalassemia is a genetic blood disorder characterized by reduced production of hemoglobin, leading to anemia. It is caused by mutations in the HBB gene, affecting the beta-globin subunit of hemoglobin. Accurate coding with ICD-10 Code D56.1 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
ICD-10 Code D56.1 represents Beta thalassemia, a hereditary condition resulting in decreased hemoglobin production. This code should be used in clinical documentation and billing when diagnosing patients with this condition, facilitating appropriate treatment plans and ensuring accurate reimbursement for healthcare services.
Beta thalassemia is caused by mutations in the HBB gene, leading to impaired synthesis of beta-globin chains. This results in an imbalance of alpha and beta chains, causing ineffective erythropoiesis and hemolytic anemia. Medical attention is crucial to manage complications such as severe anemia and iron overload.
ICD-10 Code D56.1 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans. It is relevant in both acute and chronic care settings, ensuring comprehensive care and accurate billing for services rendered.
In SOAP notes, ICD-10 Code D56.1 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Beta thalassemia. This ensures continuity of care, supports billing processes, and meets EHR documentation standards.
Beta thalassemia requires prompt medical intervention to manage symptoms and prevent complications. Treatment may include blood transfusions and chelation therapy to manage iron overload.


HIPAA-compliant and designed with privacy in mind, your patient’s data is protected. Focus on care while we safeguard your information.
Learn moreICD-10 Code D56.1 is critical in medical billing, particularly in hospital and outpatient settings for managing Beta thalassemia.
| CPT Code | Description |
|---|---|
| 36430 | Transfusion of blood products. |
| 85025 | Complete blood count with automated differential. |
| 96365 | Intravenous infusion, for therapy. |
Common Questions About Using ICD-10 Code D56.1 for Beta thalassemia
What are the common symptoms of Beta thalassemia?
Common symptoms include fatigue, weakness, pallor, and shortness of breath due to anemia. Patients may also experience splenomegaly and bone deformities.
How is Beta thalassemia diagnosed?
Diagnosis typically involves blood tests to measure hemoglobin levels, a complete blood count, and genetic testing to identify mutations in the HBB gene.
What treatments are available for Beta thalassemia?
Treatment options include regular blood transfusions, iron chelation therapy, and supportive care to manage symptoms and prevent complications.
Is Beta thalassemia hereditary?
Yes, Beta thalassemia is an inherited disorder caused by mutations in the HBB gene, and it can be passed down from parents to children.
Clinical Notes
SOAP notes
DAP notes
AI medical notes