G71.032
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
HCC risk adjustment mapping
CMS-HCC V28
Muscular Dystrophy
CMS-HCC ESRD V24
Muscular Dystrophy
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Limb girdle muscular dystrophy type 2A LGMD R1 calpain-3-related Primary calpainopathy
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)
Official Guidelines for G71.032
FY 2026 ›Find G71.032 in the alphabetic index
7 index paths lead to this code
- Calpainopathy
- Calpainopathy › autosomal recessive
- Dystrophy, dystrophia › Leyden-Möbius › meaning Limb girdle muscular dystrophy type 2A
- Dystrophy, dystrophia › muscular › limb-girdle › calpain-3-related
- Dystrophy, dystrophia › muscular › limb-girdle › R1
- Dystrophy, dystrophia › muscular › limb-girdle › type 2A
- Dystrophy, dystrophia › muscular › limb-girdle › calpain-3-related › autosomal recessive