Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia is a genetic disorder affecting red blood cell metabolism. It is caused by mutations in the G6PD gene, leading to reduced enzyme activity. Clinically significant as it can result in hemolytic anemia under oxidative stress, the ICD-10 Code D75.A facilitates accurate diagnosis, documentation, and billing, ensuring proper management and public health reporting.
ICD-10 Code D75.A represents Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia, a hereditary condition characterized by insufficient G6PD enzyme activity. This code is used in clinical documentation and billing when diagnosing patients who exhibit symptoms or have a history of G6PD deficiency but are not currently experiencing anemia.
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder that impairs the body's ability to manage oxidative stress, leading to potential hemolysis. Patients may remain asymptomatic until exposed to certain triggers, necessitating medical attention to prevent complications.
ICD-10 Code D75.A is utilized in SOAP notes to document the patient's condition accurately. It plays a crucial role in capturing symptoms, assessments, and treatment plans, relevant in both acute and chronic care settings.
In SOAP notes, ICD-10 Code D75.A connects subjective patient reports and objective clinical findings to a formal diagnosis of G6PD deficiency without anemia. This ensures continuity of care, supports billing, and meets EHR documentation standards.
Management of G6PD deficiency focuses on avoiding triggers and supportive care. Hospitalization may be necessary during hemolytic crises.


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| CPT Code | Description |
|---|---|
| 85025 | Complete blood count (CBC) with automated differential. |
| 83020 | Glucose-6-phosphate dehydrogenase (G6PD) enzyme activity test. |
| 99213 | Established patient office visit, level 3. |
Common Questions About Using ICD-10 Code D75.A for Glucose-6-phosphate dehydrgnse (G6PD) defic without anemia
What are the common triggers for G6PD deficiency?
Common triggers include certain medications (e.g., sulfa drugs), infections, and foods like fava beans. Patients should be educated on avoiding these to prevent hemolytic episodes.
Is G6PD deficiency hereditary?
Yes, G6PD deficiency is an X-linked genetic disorder, primarily affecting males. It is inherited from carrier mothers to their sons.
Can G6PD deficiency lead to serious health issues?
While many individuals remain asymptomatic, G6PD deficiency can lead to hemolytic anemia during oxidative stress, which may require medical intervention.
How is G6PD deficiency diagnosed?
Diagnosis is typically made through blood tests measuring G6PD enzyme activity. Genetic testing may also be performed for confirmation.
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