G71.032
Billable codeAutosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
The ICD-10 code for autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction is G71.032.
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.
- Limb girdle muscular dystrophy type 2A
- LGMD R1 calpain-3-related
- Primary calpainopathy
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
- G71.031Autosomal dominant limb girdle muscular dystrophy
- 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
- G71.032Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Associated MS-DRGs
G71.032 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.