- G71.032 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM G71.032 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.032 – other international versions of ICD-10 G71.032 may differ.
ICD-10-CM G71.032 is grouped within Diagnostic Related Group(s):
- 091 Other disorders of nervous system with mcc
- 092 Other disorders of nervous system with cc
- 093 Other disorders of nervous system without cc/mcc
Applicable To
- Limb girdle muscular dystrophy type 2A
- LGMD R1 calpain-3-related
- Primary calpainopathy
Code History
- 2024 (effective 10/1/2022): New code
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G71.032:
- autosomal recessive > Calpainopathy (primary) G71.032
- meaning Limb girdle muscular dystrophy type 2A (autosomal recessive) > Leyden-Möbius G71.039
- calpain-3-related > limb-girdle G71.039
- autosomal recessive > calpain-3-related G71.032
- R1 (autosomal recessive) > limb-girdle G71.039
- type 2A (autosomal recessive) > limb-girdle G71.039