G71.031
Autosomal dominant limb girdle muscular dystrophy
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
LGMD D4 calpain-3-related LGMD D5 collagen 6-related Limb girdle muscular dystrophy type 1
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 G71.031
FY 2026 ›Find G71.031 in the alphabetic index
15 index paths lead to this code
- Calpainopathy › autosomal dominant
- Dystrophy, dystrophia › muscular › limb-girdle › D1
- Dystrophy, dystrophia › muscular › limb-girdle › D2
- Dystrophy, dystrophia › muscular › limb-girdle › D3
- Dystrophy, dystrophia › muscular › limb-girdle › D4
- Dystrophy, dystrophia › muscular › limb-girdle › D5
- Dystrophy, dystrophia › muscular › limb-girdle › type 1
- Dystrophy, dystrophia › muscular › limb-girdle › type 1A
- Dystrophy, dystrophia › muscular › limb-girdle › type 1B
- Dystrophy, dystrophia › muscular › limb-girdle › type 1C
- Dystrophy, dystrophia › muscular › limb-girdle › type 1E
- Dystrophy, dystrophia › muscular › limb-girdle › type 1H
- Dystrophy, dystrophia › muscular › limb-girdle › type 1I
- Dystrophy, dystrophia › muscular › limb-girdle › calpain-3-related › autosomal dominant
- Dystrophy, dystrophia › muscular › limb-girdle › collagen VI related › autosomal dominant