Thalassemia, unspecified is a genetic blood disorder characterized by reduced hemoglobin production, leading to anemia. This condition can result in various complications, including fatigue, weakness, and increased risk of infections. Accurate coding with ICD-10 Code D56.9 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
ICD-10 Code D56.9 represents Thalassemia, unspecified, a hereditary blood disorder that affects hemoglobin synthesis. This code is used when the specific type of thalassemia is not identified. It is crucial for clinical documentation and billing, particularly when managing patients with anemia or related complications, ensuring accurate representation of the patient's condition.
Thalassemia, unspecified is caused by genetic mutations affecting hemoglobin production, leading to varying degrees of anemia. The condition can progress to severe complications if not managed properly, necessitating medical attention. Early diagnosis and treatment are vital to prevent complications such as splenomegaly and iron overload.
In SOAP notes, ICD-10 Code D56.9 is utilized to document the patient's symptoms, assessment findings, and treatment plans related to thalassemia. This code is relevant in both acute and chronic care settings, facilitating comprehensive patient management and ensuring accurate billing.
ICD-10 Code D56.9 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of thalassemia, unspecified. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Thalassemia, unspecified 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 D56.9 is critical in medical billing, particularly in hospital and emergency care settings for patients with thalassemia.
| CPT Code | Description |
|---|---|
| 36430 | Blood transfusion, per unit |
| 85027 | Complete blood count (CBC) with automated differential |
| 96365 | Intravenous infusion, for therapy, prophylaxis, or diagnosis |
Common Questions About Using ICD-10 Code D56.9 for Thalassemia, unspecified
What are the common symptoms of thalassemia?
Common symptoms of thalassemia include fatigue, weakness, pallor, and shortness of breath. Patients may also experience splenomegaly and increased susceptibility to infections due to anemia.
How is thalassemia diagnosed?
Thalassemia is diagnosed through blood tests that measure hemoglobin levels, red blood cell counts, and genetic testing to identify specific mutations affecting hemoglobin production.
What treatments are available for thalassemia?
Treatment options for thalassemia include regular blood transfusions, iron chelation therapy, and supportive care measures such as folic acid supplementation and monitoring for complications.
Is thalassemia a hereditary condition?
Yes, thalassemia is a hereditary blood disorder caused by genetic mutations that affect hemoglobin production, often passed down through families.
Clinical Notes
SOAP notes
DAP notes
AI medical notes