ICD-10 Code for Calpainopathy

Also indexed as (primary)

The ICD-10-CM code for calpainopathy is G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. This is the code the Alphabetic Index gives for calpainopathy with no further qualifier, valid for FY2027 (October 1, 2026 – September 30, 2027).

Billable

Which calpainopathy code should you use?

The Alphabetic Index lists 2 codes under Calpainopathy. Which one applies depends on the qualifier documented in the record — the type, site, cause, or associated condition. Find the qualifier below, then verify the code in the Tabular List before using it.

By type

autosomal dominant	G71.031	Autosomal dominant limb girdle muscular dystrophy
autosomal recessive	G71.032	Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

Index terms and codes are reproduced from the official ICD-10-CM FY2027 release. The Alphabetic Index is a finding aid — a code must always be verified in the Tabular List before it is reported. Data sources