Congenital methemoglobinemia is a rare genetic disorder characterized by the presence of methemoglobin in the blood, which impairs the ability of hemoglobin to carry oxygen. This condition can lead to cyanosis and other serious complications. Accurate coding with ICD-10 Code D74.0 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that affected individuals receive appropriate care and management.
ICD-10 Code D74.0 represents congenital methemoglobinemia, a condition resulting from genetic mutations that affect hemoglobin's ability to bind oxygen. This code should be used in clinical documentation and billing when diagnosing patients with this disorder, ensuring accurate representation of the patient's health status and facilitating appropriate treatment and management.
Congenital methemoglobinemia is primarily caused by inherited enzyme deficiencies, such as cytochrome b5 reductase deficiency, leading to elevated levels of methemoglobin in the blood. This condition can result in significant hypoxia and requires prompt medical attention to prevent severe complications.
ICD-10 Code D74.0 is utilized in SOAP notes 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 facilitating continuity of care.
In SOAP notes, ICD-10 Code D74.0 connects subjective reports of symptoms and objective clinical findings to a formal diagnosis of congenital methemoglobinemia. This code is crucial for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Congenital methemoglobinemia may require hospitalization for severe cases, particularly when oxygen saturation levels are critically low. Treatment focuses on reducing methemoglobin levels and managing symptoms.


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Learn moreICD-10 Code D74.0 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture. |
| 85025 | Complete blood count with automated differential. |
| 96372 | Therapeutic, prophylactic, or diagnostic injection. |
Common Questions About Using ICD-10 Code D74.0 for Congenital methemoglobinemia
What are the symptoms of congenital methemoglobinemia?
Symptoms include cyanosis, fatigue, and developmental delays. Patients may exhibit bluish discoloration of the skin, particularly in the lips and extremities, due to reduced oxygen levels in the blood.
How is congenital methemoglobinemia diagnosed?
Diagnosis is typically made through clinical evaluation and laboratory tests that measure methemoglobin levels in the blood. A thorough patient history and family history are also important.
What treatments are available for congenital methemoglobinemia?
Treatment may involve the administration of methylene blue for acute episodes and supplemental oxygen to manage hypoxia. Ongoing monitoring and patient education are also essential.
Is congenital methemoglobinemia hereditary?
Yes, congenital methemoglobinemia is usually inherited in an autosomal recessive pattern, meaning both parents must carry the gene mutation for a child to be affected.
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