ICD-10-CM Diagnosis Code (2025)
Official Description for G71.032
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Coding Notes & Guidelines for G71.032
- Limb girdle muscular dystrophy type 2A
- LGMD R1 calpain-3-related
- Primary calpainopathy
Parent Code (Less Specific):
About ICD-10-CM Code G71.032 (Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction)
ICD-10-CM code G71.032 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM G71.032 became effective on October 1, 2024.
This page provides detailed information about G71.032 - Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction.