G71.031
Billable codeAutosomal dominant limb girdle muscular dystrophy
The ICD-10 code for autosomal dominant limb girdle muscular dystrophy is G71.031.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- 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 dysfunctionnon-billable header
- 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
- G71.031Autosomal dominant limb girdle muscular dystrophy
Associated MS-DRGs
G71.031 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.