Back to HomeBeta

ICD-10 Coding for Homocysteine Disorders(E72.11, R79.83, E72.12)

Complete ICD-10-CM coding and documentation guide for Homocysteine Disorders. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

HyperhomocysteinemiaHomocystinuriaMTHFR Deficiency

Related ICD-10 Code Ranges

Complete code families applicable to Homocysteine Disorders

E72.1-E72.12Primary Range

Disorders of sulfur-bearing amino-acid metabolism

This range includes genetic and acquired disorders affecting homocysteine metabolism.

Abnormal findings of blood amino-acid levels

Used for elevated homocysteine levels without a specified genetic disorder.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
E72.11HomocystinuriaUse when genetic testing confirms homocystinuria.
  • Plasma homocysteine >100 µmol/L
  • CBS gene mutation analysis
R79.83Abnormal blood amino-acid levelUse for elevated homocysteine levels without genetic disorder.
  • Homocysteine 15-100 µmol/L
  • Normal CBS/MTHFR
E72.12MTHFR deficiencyUse for confirmed MTHFR mutation affecting homocysteine metabolism.
  • MTHFR C677T mutation testing

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for elevated homocysteine

Essential facts and insights about Homocysteine Disorders

The ICD-10 code for elevated homocysteine is R79.83, used for abnormal blood amino-acid levels.

Primary ICD-10-CM Codes for homocysteine

Homocystinuria
Billable Code

Decision Criteria

clinical Criteria

  • Genetic testing confirms CBS mutation.

Applicable To

  • Cystathionine beta-synthase deficiency

Excludes

  • Hyperhomocysteinemia without genetic confirmation

Clinical Validation Requirements

  • Plasma homocysteine >100 µmol/L
  • CBS gene mutation analysis

Code-Specific Risks

  • Incorrectly coding without genetic confirmation.

Coding Notes

  • Ensure genetic confirmation is documented.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Family history of other specified conditions

Z84.89
Use if family history of genetic disorders is documented.

Vitamin B12 deficiency

E53.8
Use if B12 deficiency is the cause.

Endocrine/metabolic disorder complicating pregnancy

O99.28
Use if MTHFR affects pregnancy.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Abnormal blood amino-acid level

R79.83
Use R79.83 for elevated homocysteine without genetic confirmation.

Homocystinuria

E72.11
Use E72.11 if genetic disorder is confirmed.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Homocysteine Disorders to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code E72.11.

Impact

Clinical: Misleading diagnosis leading to inappropriate treatment., Regulatory: Non-compliance with coding standards., Financial: Potential claim rejections.

Mitigation Strategy

Verify genetic testing results, Educate staff on coding guidelines

Impact

Reimbursement: May lead to claim denials., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate clinical data representation.

Mitigation Strategy

Ensure genetic testing is documented before using E72.11.

Impact

Risk of coding genetic disorders without confirmation.

Mitigation Strategy

Require genetic test documentation before coding.

Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.

Frequently Asked Questions

Common questions about ICD-10 coding for Homocysteine Disorders, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Homocysteine Disorders

Use these documentation templates to ensure complete and accurate documentation for Homocysteine Disorders. These templates include all required elements for proper coding and billing.

Progress Note for Hyperhomocysteinemia

Specialty: Endocrinology

Required Elements

  • Assessment of homocysteine levels
  • Underlying cause identification
  • Treatment plan

Example Documentation

**Assessment**: Hyperhomocysteinemia secondary to B12 deficiency. Homocysteine level: 32 µmol/L. **Plan**: B12 supplementation.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Patient with high homocysteine.
Good Documentation Example
Homocysteine 45 µmol/L with vitamin B12 150 pg/mL. Hyperhomocysteinemia secondary to B12 deficiency.
Explanation
The good example specifies the homocysteine level and underlying cause.

Need help with ICD-10 coding for Homocysteine Disorders? Ask your questions below.

Ask about any ICD-10 CM code, or paste a medical note

We build tools for
clinician happiness.

Learn More at Freed.ai
Back to HomeBeta

Built by Freed

Try Freed for free for 7 days.

Learn more