Biotinidase deficiency is a rare inherited metabolic disorder caused by a deficiency of the enzyme biotinidase, which is essential for the recycling of biotin, a B-vitamin. This condition leads to a range of clinical manifestations, including neurological impairment, skin rashes, and immunodeficiency. Accurate coding with ICD-10 Code D81.810 is crucial for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that affected individuals receive appropriate care and management.
ICD-10 Code D81.810 represents Biotinidase deficiency, a genetic disorder characterized by the body's inability to recycle biotin due to a deficiency in the enzyme biotinidase. This code should be used in clinical documentation and billing when diagnosing patients with this condition, particularly when symptoms such as neurological issues or skin problems are present, ensuring accurate representation of the patient's health status.
Biotinidase deficiency is caused by mutations in the BTD gene, leading to a deficiency of the biotinidase enzyme. This condition can progress to severe neurological and immunological complications if left untreated, necessitating prompt medical attention and intervention.
ICD-10 Code D81.810 is utilized in SOAP notes to document the clinical presentation, assessment, and treatment of patients with Biotinidase deficiency. This code plays a vital role 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 D81.810 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Biotinidase deficiency. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Biotinidase deficiency requires urgent medical intervention, often necessitating hospitalization for severe cases. Treatment primarily involves biotin supplementation to manage symptoms and prevent complications.


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Learn moreICD-10 Code D81.810 is critical in medical billing, particularly in hospital, emergency room, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 83000 | Biotin level test. |
| 99213 | Established patient office visit, level 3. |
| 99406 | Smoking and tobacco use cessation counseling visit. |
Common Questions About Using ICD-10 Code D81.810 for Biotinidase deficiency
What are the symptoms of Biotinidase deficiency?
Symptoms of Biotinidase deficiency can include neurological issues such as seizures, developmental delays, skin rashes, and hair loss. Early diagnosis and treatment are crucial to prevent severe complications.
How is Biotinidase deficiency diagnosed?
Diagnosis is typically made through newborn screening tests that measure biotin levels and confirm the deficiency through genetic testing. Clinical symptoms also play a significant role in diagnosis.
What is the treatment for Biotinidase deficiency?
The primary treatment for Biotinidase deficiency is high-dose biotin supplementation. Regular monitoring and supportive care are also essential to manage symptoms and prevent complications.
Is Biotinidase deficiency hereditary?
Yes, Biotinidase deficiency is an autosomal recessive genetic disorder, meaning that both parents must carry the mutated gene for a child to be affected.
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