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ICD-10 Guide
ICD-10 CodesE72.5

E72.5

Billable

Disorders of glycine metabolism

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

Code Description

ICD-10 E72.5 is a billable code used to indicate a diagnosis of disorders of glycine metabolism.

Key Diagnostic Point:

Disorders of glycine metabolism encompass a range of metabolic conditions characterized by the abnormal metabolism of glycine, an amino acid that plays a crucial role in various physiological processes, including neurotransmission and the synthesis of proteins. These disorders can arise from enzyme deficiencies that disrupt the normal catabolism of glycine, leading to its accumulation in the body. Clinical manifestations may include neurological symptoms such as seizures, developmental delays, and cognitive impairments, as well as metabolic disturbances. Genetic mutations affecting enzymes involved in glycine metabolism, such as glycine decarboxylase or serine hydroxymethyltransferase, are often implicated in these conditions. Diagnosis typically involves biochemical testing to measure glycine levels in blood and urine, alongside genetic testing to identify specific mutations. Management strategies may include dietary modifications, supplementation, and symptomatic treatment to address neurological and metabolic complications. Early diagnosis and intervention are critical to improving outcomes for affected individuals.

Code Complexity Analysis

Complexity Rating: Medium

Medium Complexity

Complexity Factors

  • Variety of underlying genetic mutations
  • Need for biochemical testing for accurate diagnosis
  • Potential overlap with other amino acid disorders
  • Variability in clinical presentation

Audit Risk Factors

  • Inadequate documentation of biochemical testing results
  • Failure to specify the type of glycine metabolism disorder
  • Lack of genetic testing documentation
  • Misclassification with other amino acid disorders

Specialty Focus

Medical Specialties

Genetics

Documentation Requirements

Detailed family history and genetic testing results must be documented.

Common Clinical Scenarios

Patients presenting with unexplained neurological symptoms or developmental delays.

Billing Considerations

Genetic counseling may be necessary for families, and documentation should reflect the need for interdisciplinary care.

Pediatrics

Documentation Requirements

Growth and developmental assessments, along with neurological evaluations.

Common Clinical Scenarios

Infants or children with developmental delays or seizures.

Billing Considerations

Close monitoring of growth parameters and developmental milestones is essential.

Coding Guidelines

Inclusion Criteria

Use E72.5 When
  • According to ICD
  • 10 coding guidelines, E72
  • 5 should be used when there is a confirmed diagnosis of a glycine metabolism disorder
  • Documentation must include biochemical and genetic testing results, as well as clinical symptoms

Exclusion Criteria

Do NOT use E72.5 When
  • Exclusion criteria include other metabolic disorders that may present similarly

Related ICD-10 Codes

Related CPT Codes

81240CPT Code

Genetic testing for glycine decarboxylase deficiency

Clinical Scenario

Used when a patient is suspected of having a glycine metabolism disorder.

Documentation Requirements

Documentation of clinical symptoms and rationale for genetic testing.

Specialty Considerations

Genetic counseling may be necessary for families.

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, including disorders of glycine metabolism. This specificity aids in better tracking of these conditions and improves the accuracy of treatment and management data.

ICD-9 vs ICD-10

The transition to ICD-10 has allowed for more specific coding of metabolic disorders, including disorders of glycine metabolism. This specificity aids in better tracking of these conditions and improves the accuracy of treatment and management data.

Reimbursement & Billing Impact

reimbursement.

Resources

Clinical References

  • •
    National Organization for Rare Disorders (NORD)

Coding & Billing References

  • •
    National Organization for Rare Disorders (NORD)

Frequently Asked Questions

What are the common symptoms of disorders of glycine metabolism?

Common symptoms include developmental delays, seizures, cognitive impairments, and metabolic disturbances. The severity and type of symptoms can vary widely among individuals.