G71.035
Limb girdle muscular dystrophy due to anoctamin-5 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
Anoctamin-5-related LGMD R12 Anoctaminopathy Autosomal recessive limb girdle muscular dystrophy type 2L Miyoshi myopathy type 3
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 G71.035
FY 2026 ›Find G71.035 in the alphabetic index
6 index paths lead to this code
- Anoctaminopathy
- Myopathy › Miyoshi, type 3
- Dystrophy, dystrophia › muscular › limb-girdle › anoctamin-5-related autosomal recessive
- Dystrophy, dystrophia › muscular › limb-girdle › R12
- Dystrophy, dystrophia › muscular › limb-girdle › type 2L
- Dystrophy, dystrophia › muscular › limb-girdle › due to › anoctamin-5 dysfunction