NPI Atlas

ICD-10 Code for Calpainopathy

The default ICD-10-CM 2027 code for calpainopathy (primary) is G71.032 – Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. More specific codes depend on the details documented, as listed in the official index (2 codes, 2 billable).

Main code: G71.032 – Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Billable: Yes

Index entries for Calpainopathy

autosomal dominant – G71.031
autosomal recessive – G71.032

How to choose the right code

Start with the main term, then pick the indented subterm that matches the documentation (type, cause, site, laterality, episode of care). Always confirm the code in the tabular list: follow its Excludes1/Excludes2, “code first” and “use additional code” notes, and add a 7th character where required.

Source: CDC/NCHS ICD-10-CM FY2027 alphabetic index.