Back to HomeBeta

ICD-10 Coding for Osteogenesis Imperfecta Congenita(Q78.0)

Complete ICD-10-CM coding and documentation guide for Osteogenesis Imperfecta Congenita. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

Brittle Bone DiseaseOIC

Related ICD-10 Code Ranges

Complete code families applicable to Osteogenesis Imperfecta Congenita

Q78.0Primary Range

Osteogenesis imperfecta

This code covers all types of osteogenesis imperfecta, including congenital forms.

Pathological fracture in diseases classified elsewhere

Used for coding fractures associated with osteogenesis imperfecta.

Diseases of the ear and mastoid process

Relevant for coding hearing loss associated with osteogenesis imperfecta.

Hereditary disturbances in tooth structure, not elsewhere classified

Used for coding dentinogenesis imperfecta, a common feature in osteogenesis imperfecta.

Key Information: ICD-10 code for osteogenesis imperfecta congenita

Essential facts and insights about Osteogenesis Imperfecta Congenita

The ICD-10 code for osteogenesis imperfecta congenita is Q78.0.

Primary ICD-10-CM Code for osteogenesis imperfecta congenita

Osteogenesis imperfecta
Billable Code

Decision Criteria

clinical Criteria

  • Presence of multiple fractures with minimal trauma and blue sclerae

coding Criteria

  • Use Q78.0 as primary code for all types of osteogenesis imperfecta

documentation Criteria

  • Document genetic testing results and clinical features

Applicable To

  • Osteogenesis imperfecta congenita
  • Osteogenesis imperfecta tarda

Excludes

  • Other specified congenital malformations of musculoskeletal system (Q79.8)

Clinical Validation Requirements

  • Genetic testing confirming COL1A1 or COL1A2 mutation
  • Clinical presentation of multiple fractures with minimal trauma
  • Presence of blue sclerae

Code-Specific Risks

  • Misclassification if type is not specified in documentation

Coding Notes

  • Ensure documentation specifies type and associated conditions for accurate coding.

Ancillary Codes

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

Pathological fracture in diseases classified elsewhere

M84.5
Use for coding fractures associated with osteogenesis imperfecta.

Diseases of the ear and mastoid process

H90-H95
Use for coding hearing loss associated with osteogenesis imperfecta.

Hereditary disturbances in tooth structure, not elsewhere classified

K00.5
Use for coding dentinogenesis imperfecta associated with osteogenesis imperfecta.

Differential Codes

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

Suspected child abuse, initial encounter

T74.12XA
Differentiate based on clinical signs of OI such as blue sclerae and genetic testing.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Osteogenesis Imperfecta Congenita to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code Q78.0.

Impact

Clinical: May lead to misdiagnosis., Regulatory: Non-compliance with coding standards., Financial: Potential for denied claims.

Mitigation Strategy

Ensure genetic testing is ordered and results documented., Educate staff on importance of genetic documentation.

Impact

Reimbursement: Incorrect coding may lead to denied claims., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate clinical data representation.

Mitigation Strategy

Use specific fracture codes from M84.5 range when fractures are part of OI.

Impact

Incorrect coding of fractures associated with OI.

Mitigation Strategy

Ensure documentation specifies fracture relation to OI.

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 Osteogenesis Imperfecta Congenita, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Osteogenesis Imperfecta Congenita

Use these documentation templates to ensure complete and accurate documentation for Osteogenesis Imperfecta Congenita. These templates include all required elements for proper coding and billing.

Newborn with suspected OI

Specialty: Pediatrics

Required Elements

  • Family history of OI
  • Presence of blue sclerae
  • Genetic testing results
  • Fracture history

Example Documentation

Newborn presents with multiple fractures and blue sclerae. Family history positive for OI. Genetic testing confirms COL1A1 mutation.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Newborn with fractures.
Good Documentation Example
Newborn with multiple fractures, blue sclerae, and confirmed COL1A1 mutation.
Explanation
The good example provides specific clinical details and genetic confirmation, improving coding accuracy.

Need help with ICD-10 coding for Osteogenesis Imperfecta Congenita? 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