Congenital agranulocytosis is a rare genetic disorder characterized by the absence of neutrophils, leading to severe immunodeficiency. This condition is critical as it increases susceptibility to infections, necessitating accurate diagnosis and management. The ICD-10 Code D70.0 facilitates precise documentation, billing, and public health reporting, ensuring that affected individuals receive appropriate care and monitoring.
ICD-10 Code D70.0 represents Congenital agranulocytosis, a condition resulting from genetic mutations that impair the production of neutrophils in the bone marrow. This code should be used in clinical documentation and billing when diagnosing patients with this condition, ensuring proper identification of the underlying disease and facilitating appropriate treatment and management strategies.
Congenital agranulocytosis is primarily caused by inherited genetic defects that disrupt normal hematopoiesis, leading to a significant reduction in neutrophil count. This condition requires immediate medical attention due to the heightened risk of severe infections. Early diagnosis and intervention are crucial for improving patient outcomes.
In SOAP notes, ICD-10 Code D70.0 is utilized to document the patient's symptoms, assessment findings, and treatment plans. This code is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and guiding clinical decision-making.
ICD-10 Code D70.0 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of congenital agranulocytosis. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Congenital agranulocytosis often necessitates hospitalization due to the risk of life-threatening infections. Treatment may include specific therapies to manage the condition and prevent complications.


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Learn moreICD-10 Code D70.0 is crucial for billing in hospital, emergency room, or infectious disease care settings, ensuring accurate representation of the patient's condition.
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture. |
| 85025 | Complete blood count with automated differential. |
| 85027 | Complete blood count with manual differential. |
| 88305 | Pathology examination of tissue, including bone marrow biopsy. |
Common Questions About Using ICD-10 Code D70.0 for Congenital agranulocytosis
What are the common symptoms of congenital agranulocytosis?
Common symptoms include recurrent infections, fever, oral ulcers, and skin lesions. Patients may also experience fatigue and failure to thrive, particularly in infants and children.
How is congenital agranulocytosis diagnosed?
Diagnosis is typically made through blood tests showing severe neutropenia and a bone marrow biopsy confirming the absence of neutrophil precursors. Family history may also provide important diagnostic clues.
What treatment options are available for congenital agranulocytosis?
Treatment includes broad-spectrum antibiotics to manage infections, supportive care to enhance immune function, and regular monitoring of blood counts. In severe cases, hospitalization may be required.
Is congenital agranulocytosis hereditary?
Yes, congenital agranulocytosis is often caused by genetic mutations that affect neutrophil production, making it a hereditary condition that can run in families.
Clinical Notes
SOAP notes
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