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ICD-10 Guide
ICD-10 CodesE72.23

E72.23

Billable

Citrullinemia

BILLABLE STATUSYes
IMPLEMENTATION DATEOctober 1, 2015
LAST UPDATED09/05/2025

Code Description

ICD-10 E72.23 is a billable code used to indicate a diagnosis of citrullinemia.

Key Diagnostic Point:

Citrullinemia is a rare genetic metabolic disorder characterized by a deficiency of the enzyme argininosuccinate synthetase, which is crucial for the urea cycle. This enzyme deficiency leads to an accumulation of citrulline in the blood and a deficiency of arginine, resulting in hyperammonemia, which can cause severe neurological damage if not treated promptly. Symptoms often present in infancy or early childhood and may include vomiting, lethargy, irritability, and seizures. In some cases, individuals may experience episodes of metabolic decompensation triggered by illness, fasting, or high-protein intake. Long-term management typically involves dietary restrictions to limit protein intake and supplementation with arginine to help manage ammonia levels. Early diagnosis through newborn screening programs is critical for improving outcomes, as timely intervention can prevent severe complications associated with elevated ammonia levels.

Code Complexity Analysis

Complexity Rating: Medium

Medium Complexity

Complexity Factors

  • Requires understanding of metabolic pathways and urea cycle disorders.
  • Differentiation from other amino acid disorders can be challenging.
  • Documentation must specify enzyme deficiency and clinical manifestations.
  • Management strategies may vary significantly based on patient age and symptoms.

Audit Risk Factors

  • Inadequate documentation of enzyme deficiency.
  • Failure to document clinical symptoms and management strategies.
  • Misclassification of the disorder as a more common condition.
  • Lack of follow-up documentation for ongoing management.

Specialty Focus

Medical Specialties

Pediatrics

Documentation Requirements

Detailed clinical history, including onset of symptoms and dietary management.

Common Clinical Scenarios

Infants presenting with vomiting and lethargy, requiring metabolic workup.

Billing Considerations

Close monitoring of growth and development in affected children.

Genetics

Documentation Requirements

Genetic testing results and family history of metabolic disorders.

Common Clinical Scenarios

Counseling families with a history of citrullinemia or related disorders.

Billing Considerations

Understanding of inheritance patterns and implications for siblings.

Coding Guidelines

Inclusion Criteria

Use E72.23 When
  • Follow official ICD
  • 10 coding guidelines, ensuring accurate documentation of the condition's clinical manifestations and management
  • Include any relevant laboratory findings and genetic testing results

Exclusion Criteria

Do NOT use E72.23 When
No specific exclusions found.

Related ICD-10 Codes

Related CPT Codes

81200CPT Code

Genetic testing for citrullinemia

Clinical Scenario

Used when confirming a diagnosis of citrullinemia through genetic analysis.

Documentation Requirements

Document the necessity of genetic testing based on clinical presentation.

Specialty Considerations

Genetic specialists should ensure comprehensive family history is included.

ICD-10 Impact

Diagnostic & Documentation Impact

Enhanced Specificity

ICD-10 Improvements

The transition to ICD-10 has allowed for more specific coding of metabolic disorders like citrullinemia, improving the accuracy of data collection and reimbursement processes.

ICD-9 vs ICD-10

The transition to ICD-10 has allowed for more specific coding of metabolic disorders like citrullinemia, improving the accuracy of data collection and reimbursement processes.

Reimbursement & Billing Impact

reimbursement processes.

Resources

Clinical References

  • •
    National Organization for Rare Disorders (NORD)

Coding & Billing References

  • •
    National Organization for Rare Disorders (NORD)

Frequently Asked Questions

What are the primary symptoms of citrullinemia?

Primary symptoms include vomiting, lethargy, irritability, and seizures, particularly during metabolic crises.

How is citrullinemia diagnosed?

Diagnosis is typically made through newborn screening tests that reveal elevated citrulline levels, followed by confirmatory genetic testing.

What management strategies are used for citrullinemia?

Management includes dietary restrictions to limit protein intake and supplementation with arginine to help manage ammonia levels.