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ICD-10-CM Codes
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2023 ICD-10-CM Diagnosis Code G72.41
2023 ICD-10-CM Diagnosis Code G72.41
Inclusion body myositis [IBM]
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- G72.41 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM G72.41 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G72.41 - other international versions of ICD-10 G72.41 may differ.
The following code(s) above
G72.41 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
G72.41:
- Inclusion body myositis
- Myositis, inclusion body
Clinical Information
- An acquired or hereditary chronic inflammatory disorder of the muscles characterized by the morphologic finding of vacuoles and filamentous inclusions in the muscle tissues.
- Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
ICD-10-CM G72.41 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 545 Connective tissue disorders with mcc
- 546 Connective tissue disorders with cc
- 547 Connective tissue disorders without cc/mcc
Convert G72.41 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to G72.41:
- Myositis M60.9
ICD-10-CM Diagnosis Code M60.9
Myositis, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- inclusion body [IBM] G72.41
ICD-10-CM Codes Adjacent To G72.41
G71.29 Other congenital myopathy
G71.3 Mitochondrial myopathy, not elsewhere classified
G71.8 Other primary disorders of muscles
G71.9 Primary disorder of muscle, unspecified
G72 Other and unspecified myopathies
G72.0 Drug-induced myopathy
G72.2 Myopathy due to other toxic agents
G72.4 Inflammatory and immune myopathies, not elsewhere classified
G72.41
Inclusion body myositis [IBM]
G72.49 Other inflammatory and immune myopathies, not elsewhere classified
G72.8 Other specified myopathies
G72.81 Critical illness myopathy
G72.89 Other specified myopathies
G72.9 Myopathy, unspecified
G73 Disorders of myoneural junction and muscle in diseases classified elsewhere
G73.1 Lambert-Eaton syndrome in neoplastic disease
G73.3 Myasthenic syndromes in other diseases classified elsewhere
G73.7 Myopathy in diseases classified elsewhere
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
