Familial erythrocytosis is a genetic condition characterized by an increased production of red blood cells, leading to elevated hemoglobin and hematocrit levels. This condition is clinically significant as it can predispose individuals to thrombotic events and other complications. The ICD-10 Code D75.0 facilitates accurate diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and management.
ICD-10 Code D75.0 represents familial erythrocytosis, a hereditary disorder resulting in excessive red blood cell production. This code should be used in clinical documentation and billing when diagnosing patients with this condition, particularly when there is a family history or genetic predisposition involved.
Familial erythrocytosis is primarily caused by genetic mutations that lead to increased erythropoietin production or sensitivity. This condition can progress to complications such as hypertension and thromboembolic events, necessitating medical attention for management and monitoring.
ICD-10 Code D75.0 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 documentation of the patient's condition.
In SOAP notes, ICD-10 Code D75.0 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of familial erythrocytosis. This code supports continuity of care, facilitates billing, and meets EHR documentation standards.
Familial erythrocytosis may require hospitalization for severe cases, particularly if complications arise. Treatment focuses on managing symptoms and preventing thrombotic events.


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Learn moreICD-10 Code D75.0 is crucial for billing in hospital, ER, or outpatient settings, ensuring proper reimbursement for services rendered.
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture |
| 85025 | Complete blood count with automated differential |
| 36416 | Collection of capillary blood specimen (e.g., heel or finger stick) |
Common Questions About Using ICD-10 Code D75.0 for Familial erythrocytosis
What are the common symptoms of familial erythrocytosis?
Common symptoms include fatigue, headaches, dizziness, and a ruddy complexion. Patients may also experience complications such as hypertension and thrombotic events.
How is familial erythrocytosis diagnosed?
Diagnosis is typically made through blood tests showing elevated hemoglobin and hematocrit levels, along with a thorough family history assessment.
What treatments are available for familial erythrocytosis?
Treatment often involves phlebotomy to reduce red blood cell mass, along with hydration and monitoring for complications.
Is familial erythrocytosis hereditary?
Yes, familial erythrocytosis is a genetic condition, often passed down through families, leading to increased red blood cell production.
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