G71.032

Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

Billable

Code Hierarchy

Coding Guidelines

Inclusion Terms

  • Limb girdle muscular dystrophy type 2A
  • LGMD R1 calpain-3-related
  • Primary calpainopathy

Get started with Scope today

Spend more time caring for patients, not charting. Scope captures your patient encounters in real time and quickly generates high-quality clinical notes – and it's completely free.

AnneLisaDavid
1k+

from 1k+ happy clinicians

Get started now