Hereditary hemolytic anemia, unspecified, is a genetic disorder characterized by the premature destruction of red blood cells, leading to anemia. This condition can result from various inherited defects affecting red blood cell membranes, enzymes, or hemoglobin. Accurate coding with ICD-10 Code D58.9 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
ICD-10 Code D58.9 represents hereditary hemolytic anemia that is unspecified, indicating a genetic predisposition to anemia due to the destruction of red blood cells. This code should be used when the specific type of hereditary hemolytic anemia is not identified. It is crucial for clinical documentation and billing to ensure accurate representation of the patient's condition.
Hereditary hemolytic anemia, unspecified, is caused by genetic mutations that lead to the destruction of red blood cells, resulting in anemia. The condition can progress to severe anemia if not managed appropriately, necessitating medical attention to prevent complications such as fatigue, jaundice, and splenomegaly.
ICD-10 Code D58.9 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans related to hereditary hemolytic anemia. This code is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and facilitating appropriate management.
In SOAP notes, ICD-10 Code D58.9 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of hereditary hemolytic anemia. This code supports continuity of care, aids in billing processes, and meets EHR documentation standards.
Hereditary hemolytic anemia, unspecified, may require hospitalization for severe cases. Treatment focuses on managing symptoms and preventing complications.


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Learn moreICD-10 Code D58.9 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 36430 | Blood transfusion, per unit |
| 85025 | Complete blood count (CBC) with automated differential |
| 99213 | Established patient office visit, Level 3 |
Common Questions About Using ICD-10 Code D58.9 for Hereditary hemolytic anemia, unspecified
What are the common symptoms of hereditary hemolytic anemia?
Common symptoms include fatigue, weakness, jaundice, and shortness of breath. Patients may also experience paleness and an increased heart rate due to anemia.
How is hereditary hemolytic anemia diagnosed?
Diagnosis typically involves a complete blood count (CBC), reticulocyte count, and peripheral blood smear. Genetic testing may also be performed to identify specific hereditary conditions.
What treatments are available for hereditary hemolytic anemia?
Treatment options include blood transfusions for severe anemia, folic acid supplementation, and management of underlying causes. In some cases, splenectomy may be considered.
Is hereditary hemolytic anemia contagious?
No, hereditary hemolytic anemia is not contagious as it is a genetic disorder passed down through families and not caused by infections.
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