G71.032✓ Billable
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Autosomal recessive limb girdle muscular dystrophy due to ca…
Inclusion Terms
- •Limb girdle muscular dystrophy type 2A
- •LGMD R1 calpain-3-related
- •Primary calpainopathy
Also Indexed As(ICD-10-CM Alphabetic Index)
These clinical terms, synonyms, and manifestations all map to G71.032 in the official ICD-10-CM Alphabetic Index.
Calpainopathy (primary)Calpainopathy (primary), autosomal recessiveDystrophy, dystrophia, Leyden-Möbius, meaning Limb girdle muscular dystrophy type 2A (autosomal recessive)Dystrophy, dystrophia, muscular, limb-girdle, R1 (autosomal recessive)Dystrophy, dystrophia, muscular, limb-girdle, calpain-3-relatedDystrophy, dystrophia, muscular, limb-girdle, calpain-3-related, autosomal recessiveDystrophy, dystrophia, muscular, limb-girdle, type 2A (autosomal recessive)
Code Hierarchy
┌6Diseases of the nervous system (G00-G99)├G70-G73Diseases of myoneural junction and muscle (G70-G73)├G71Primary disorders of muscles
└G71.032Autosomal recessive limb girdle muscular dystrophy due to ca…
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