G71.031 - Autosomal dominant limb girdle muscular dystrophy
- Applicable to Autosomal dominant limb girdle muscular dystrophy
- The 2025 edition of ICD10-CM G71.031 became effective on October 1, 2024.
- This is the American ICD10-CM version of G71.031 - other international versions of ICD10 G71.031 may differ.
- G71.031 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Billable/Specific Code
The following codes above G71.031 contain annotation back-references that may be applicable to G71.031:
- Chapter: G00-G99 - Diseases of the nervous system
- Section: G70-G73 - Diseases of myoneural junction and muscle
- Category: G71 - Primary disorders of muscles
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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