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ICD-10-CM Code G71.032

Official Description

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

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

Short Descr	Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct
CMS-HCC v22	76 - Muscular Dystrophy
CMS-HCC v24	76 - Muscular Dystrophy
CMS-HCC v28	197 - Muscular Dystrophy
ESRD-HCC v21	76 - Muscular Dystrophy
ESRD-HCC v24	76 - Muscular Dystrophy
HHS-HCC v07	117 - Muscular Dystrophy

G00.0-G99.8 6. Diseases of the nervous system (G00-G99)

G70.00-G73.7 G70-G73 Diseases of myoneural junction and muscle (G70-G73)

G71.00-G71.9 G71 Primary disorders of muscles

G71.00-G71.09 G71.0 Muscular dystrophy

G71.031-G71.039 G71.03 Limb girdle muscular dystrophies

G71.031 Autosomal dominant limb girdle muscular dystrophy

G71.032 Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct

G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction

G71.035 Limb girdle musc dyst due to anoctamin-5 dysfunction

G71.038 Other limb girdle muscular dystrophy

G71.039 Limb girdle muscular dystrophy, unspecified

G71.0340-G71.0349 G71.034 Limb girdle muscular dystrophy due to sarcoglycan dysfunction

Date	Action	Notes
2022-10-01	Added	Code Added.

Code	Description

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