ICD-10 Code D81.818 | Other biotin-dependent carboxylase deficiency Symptoms, Diagnosis, Billing

Other biotin-dependent carboxylase deficiency is a rare metabolic disorder caused by a deficiency of biotin-dependent carboxylases, leading to impaired fatty acid and amino acid metabolism. This condition is clinically significant as it can result in neurological symptoms, metabolic derangements, and developmental delays. The ICD-10 Code D81.818 facilitates accurate diagnosis, documentation, medical billing, and public health reporting, ensuring that healthcare providers can effectively manage and treat affected individuals.

What is ICD-10 Code D81.818 for Other biotin-dependent carboxylase deficiency?

ICD-10 Code D81.818 represents Other biotin-dependent carboxylase deficiency, a condition characterized by the body's inability to utilize biotin effectively due to enzyme deficiencies. This code should be used in clinical documentation and billing when diagnosing patients with this metabolic disorder, ensuring appropriate treatment and management strategies are implemented.

ICD-10 Code D81.818 – Clinical Definition and Explanation of Other biotin-dependent carboxylase deficiency

Other biotin-dependent carboxylase deficiency is caused by genetic mutations affecting enzymes that require biotin as a cofactor. The condition can lead to significant metabolic disturbances and requires prompt medical attention to prevent complications. Early diagnosis and intervention are crucial for improving patient outcomes.

Key Clinical Features:

• Neurological symptoms such as seizures and developmental delays.
• Metabolic acidosis and ketosis due to impaired fatty acid metabolism.
• Skin rashes and alopecia associated with biotin deficiency.
• Elevated levels of organic acids in urine.

ICD-10 Code D81.818 for Other biotin-dependent carboxylase deficiency – SOAP Notes & Clinical Use

ICD-10 Code D81.818 is utilized in SOAP notes to document the clinical presentation, assessment, and treatment of patients with Other biotin-dependent carboxylase deficiency. This code aids in capturing the patient's symptoms, guiding clinical decision-making, and ensuring appropriate billing in both acute and chronic care settings.

What Does ICD-10 Code D81.818 for Other biotin-dependent carboxylase deficiency Mean in SOAP Notes?

In SOAP notes, ICD-10 Code D81.818 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Other biotin-dependent carboxylase deficiency. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.

Treatment Options for ICD-10 Code D81.818 – Other biotin-dependent carboxylase deficiency

Management of Other biotin-dependent carboxylase deficiency requires urgent medical intervention to address metabolic imbalances and prevent complications.

Antibiotic Therapy:

Supportive Care:

• Biotin supplementation to restore enzyme function.
• Nutritional support to manage metabolic needs.
• Monitoring for metabolic derangements and neurological symptoms.

Infection Control:

How to Document Symptoms of Other biotin-dependent carboxylase deficiency (ICD-10 D81.818) in SOAP Notes

Subjective:

• Patient reports developmental delays and seizures.
• History of skin rashes and hair loss.
• Family history of metabolic disorders.

Objective:

• Neurological examination reveals developmental delays.
• Laboratory tests show metabolic acidosis and elevated organic acids.
• Physical examination indicates alopecia and dermatitis.

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SOAP Note Guidelines for Diagnosing Other biotin-dependent carboxylase deficiency (ICD-10 Code D81.818)

Assessment:

• Diagnosis: Other biotin-dependent carboxylase deficiency, moderate severity.
• ICD-10 Code: D81.818.
• Contributing factors: Genetic mutations affecting biotin metabolism.

Plan:

• Initiate biotin supplementation therapy.
• Provide dietary counseling to ensure adequate nutrient intake.
• Schedule follow-up appointments to monitor metabolic status.

Treatment & Plan Section for ICD-10 Code D81.818 – Other biotin-dependent carboxylase deficiency

• Administer biotin supplementation as per clinical guidelines.
• Implement dietary modifications to support metabolic health.
• Regularly monitor metabolic parameters and neurological status.
• Educate the patient and family about the condition and management strategies.

Using ICD-10 Code D81.818 for Other biotin-dependent carboxylase deficiency in Billing & SOAP Note Compliance

• Ensure accurate documentation of symptoms and clinical findings in SOAP notes.
• Use the code in appropriate clinical settings, including outpatient and inpatient care.
• Align treatment plans with clinical guidelines to support justified billing.
• Document any relevant comorbidities or complications to enhance coding accuracy.

Related ICD-10 Codes Often Used with Other biotin-dependent carboxylase deficiency

• D81.810 – Biotinidase deficiency

ICD-10 Code D81.818 in Medical Billing and Insurance for Other biotin-dependent carboxylase deficiency

ICD-10 Code D81.818 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.

Billing Notes:

• Document all relevant clinical findings and treatment plans to support the ICD-10 claim.
• Use the code in conjunction with appropriate CPT codes for comprehensive billing.
• Ensure that the diagnosis is clearly linked to the patient's presenting symptoms.

Common CPT Pairings: