G71032Level 5

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

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

GET/api/v1/systems/icd10cm/nodes/G71032

Official DownloadPublic Domain (US Government)Source

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