G71.032 - Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

Applicable to Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
The 2025 edition of ICD10-CM G71.032 became effective on October 1, 2024.
This is the American ICD10-CM version of G71.032 - other international versions of ICD10 G71.032 may differ.
G71.032 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

Inclusion Term

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

The following codes above G71.032 contain annotation back-references that may be applicable to G71.032:

Chapter: G00-G99 Diseases of the nervous system

Section: G70-G73 Diseases of myoneural junction and muscle

Category: G71 Primary disorders of muscles

muscular icd 10

recessive icd 10

dysfunction icd 10

dystrophy icd 10

autosomal icd 10

Billable/Specific Code

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Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

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