G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Instructional Notes:
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G71.032
Description: Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Inclusion Term:
- Limb girdle muscular dystrophy type 2A
- LGMD R1 calpain-3-related
- Primary calpainopathy
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G71.03
Description: Limb girdle muscular dystrophies
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G71.0
Description: Muscular dystrophy
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G71
Description: Primary disorders of muscles
Exclude2:
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
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G70-G73
Description: Diseases of myoneural junction and muscle (G70-G73)
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G00-G99
Description: Diseases of the nervous system
Exclude2:
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)