Billable / Specific Code
ICD-10-CM G71.032 is the diagnosis code for Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. This code falls under the section "Diseases of myoneural junction and muscle" within Chapter 6 — Diseases of the nervous system (G00-G99). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where G71.032 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, G71.032 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
G71.032 is the ICD-10-CM diagnosis code for "Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
The parent code of G71.032 is G71.03 ("Limb girdle muscular dystrophies"). G71.032 provides a more specific classification within this category.
G71.032 is located in Section G70-G73 — "Diseases of myoneural junction and muscle" within Chapter 6 of the ICD-10-CM Tabular List.
Use G71.032 when the patients documented diagnosis matches "Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction is G71.032.
Yes, G71.032 can be used as a primary diagnosis code since it is billable and specific.
G71.032 is in Chapter 6 of the ICD-10-CM Tabular List.
Yes, G71.032 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.