Is G71.032 a billable code?
Yes. G71.032 is a billable ICD-10-CM code and can be used on claims and superbills for dates of service from October 1, 2026 to September 30, 2027.
ICD-10-CM FY2027 diagnosis code
G71.032: Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Billable codeValid for dates of service October 1, 2026 to September 30, 2027
G71.032 is a billable ICD-10-CM diagnosis code for autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. It is specific enough to use on an insurance claim, a superbill or a Good Faith Estimate.
Superbill GeneratorStart a superbill with G71.032 already added.Good Faith EstimateStart a cost estimate with G71.032 already added.CMS-1500 Claim FormFill a claim form with G71.032 in box 21.
Other codes in G71.03 Limb girdle muscular dystrophies
- G71.031Autosomal dominant limb girdle muscular dystrophy
- G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.034Limb girdle muscular dystrophy due to sarcoglycan dysfunctionheader
- 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
G71.032 questions
What does G71.032 mean?
G71.032 is the ICD-10-CM code for Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. It is in chapter 6, Diseases of the nervous system (G00-G99).
Code titles come from the official ICD-10-CM files published by the CDC National Center for Health Statistics. Always check payer rules and the clinical record before billing.