G71.2 - Congenital myopathies
- Applicable to Congenital myopathies
- The 2025 edition of ICD10-CM G71.2 became effective on October 1, 2024.
- This is the American ICD10-CM version of G71.2 - other international versions of ICD10 G71.2 may differ.
- G71.2 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- G71.2 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- G71.2 - Congenital myopathies
- G71.2 - Congenital myopathies
- G71.20 - Congenital myopathy, unspecified
- G71.21 - Nemaline myopathy
- G71.22 - Centronuclear myopathy
- G71.220 - X-linked myotubular myopathy
- G71.228 - Other centronuclear myopathy
- G71.29 - Other congenital myopathy
Type 2 Excludes
- arthrogryposis multiplex congenita (Q74.3)
The following codes above G71.2 contain annotation back-references that may be applicable to G71.2:
Chapter: G00-G99 Diseases of the nervous system
Section: G70-G73 Diseases of myoneural junction and muscle
Category: G71 Primary disorders of muscles
Non-Billable/Non-Specific Code
Browse other similar CM codes
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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