ICD-10-CM · Chapter 6 · G00–G99
G71.032
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Diseases of the nervous system
Quick facts
- Code
- G71.032
- Type
- Billable code
- ICD-10-CM chapter
- Chapter 6 — Diseases of the nervous system
- Category
- G71 — Primary disorders of muscles
- Specificity
- 6 characters
How coders use this code
ICD-10-CM G71.032 is a billable, fully specified code, so it can be reported directly on a claim to document a diagnosis of autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. Coders assign it when the chart documentation supports this level of detail, always matching to the most specific code available and verifying against the chapter-specific guidelines published annually by NCHS/CMS.
Related codes in G71
- G71Primary disorders of muscles
- G71.0Muscular dystrophy
- G71.00Muscular dystrophy, unspecified
- G71.01Duchenne or Becker muscular dystrophy
- G71.02Facioscapulohumeral muscular dystrophy
- G71.03Limb 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 dysfunction
- G71.0340Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
- G71.0341Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- G71.0342Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- G71.0349Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- G71.035Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- G71.036Limb girdle muscular dystrophy due to fukutin related protein dysfunction
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