G71.032 AUTOSOM RECESS LIMB GIRDLE MUSC DYST D/T CALPAIN-3 DYSFNCT

Code Information

Diagnosis Code: G71.032

Short Description: Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct

Long Description: Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

The code G71.032 is VALID for claim submission

Code Classification:

Diseases of the nervous system (G00–G99)
- Diseases of myoneural junction and muscle (G70-G73)
  - Primary disorders of muscles (G71)
    - G71.032 Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct

Code Version: 2022 ICD-10-CM

The code G71.032 has the following ICD-10-CM references to the Index of Diseases and Injuries

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

ICD-10 Code	ICD-10 Description
G71	Primary disorders of muscles
G71.0	Muscular dystrophy
G71.00	Muscular dystrophy, unspecified
G71.01	Duchenne or Becker muscular dystrophy
G71.02	Facioscapulohumeral muscular dystrophy
G71.03	Limb girdle muscular dystrophies
G71.031	Autosomal dominant limb girdle muscular dystrophy
G71.033	Limb girdle muscular dystrophy due to dysferlin dysfunction
G71.034	Limb girdle muscular dystrophy due to sarcoglycan dysfunction
G71.0340	Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
G71.0341	Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
G71.0342	Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
G71.0349	Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
G71.035	Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
G71.038	Other limb girdle muscular dystrophy
G71.039	Limb girdle muscular dystrophy, unspecified
G71.09	Other specified muscular dystrophies
G71.1	Myotonic disorders
G71.11	Myotonic muscular dystrophy
G71.12	Myotonia congenita
G71.13	Myotonic chondrodystrophy
G71.14	Drug induced myotonia
G71.19	Other specified myotonic disorders
G71.2	Congenital myopathies
G71.20	Congenital myopathy, unspecified
G71.21	Nemaline myopathy
G71.22	Centronuclear myopathy
G71.220	X-linked myotubular myopathy
G71.228	Other centronuclear myopathy
G71.29	Other congenital myopathy
G71.3	Mitochondrial myopathy, not elsewhere classified
G71.8	Other primary disorders of muscles
G71.9	Primary disorder of muscle, unspecified

This page was last updated on: 10/1/2023