G71.031
G71.031: Autosomal dominant limb girdle muscular dystrophy
Billable / specific codeICD-10-CM
G71.031 is a billable, specific ICD-10-CM code for autosomal dominant limb girdle muscular dystrophy. It is valid for submission on a claim.
Check G71.031 with the rest of the claim: free scrubberInclusion terms
Alternative wordings a physician may use in the chart for this same code.
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Risk adjustment
G71.031 risk-adjusts. Under the CMS-HCC V28 model it maps to this category:
- HCC 197 Muscular Dystrophy0.426 RAF
Coefficient shown for the Community Non-dual Aged segment. A higher HCC in the same hierarchy will suppress this one, so capturing it does not always add score. Look up the whole chart to see which of its HCCs the hierarchy would zero.
Medicare coverage
G71.031 is named in 15 Medicare coverage policies: 15 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A52494High Frequency Chest Wall Oscillation Devices - Policy Article
- A52510Mechanical In-exsufflation Devices - Policy Article
- A53057Billing and Coding: Home Health Occupational Therapy
- A53058Billing and Coding: Home Health Physical Therapy
Alphabetic index entries that lead here
- Calpainopathy›autosomal dominant
- Dystrophy, dystrophia›muscular›limb-girdle›D1(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›D2(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›D3(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›D4(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›D5(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1A(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1B(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1C(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1E(autosomal dominant)
- Dystrophy, dystrophia›muscular›limb-girdle›type 1H(autosomal dominant)
Code history
Unchanged in every release from FY2024 to FY2027.
Other codes under G71.03
- G71.032Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.034Limb girdle muscular dystrophy due to sarcoglycan dysfunction
- G71.035Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- G71.036Limb girdle muscular dystrophy due to fukutin related protein dysfunction
- G71.038Other limb girdle muscular dystrophy
- G71.039Limb girdle muscular dystrophy, unspecified