Coding and coverage · ICD-10-CM
G71.03 Limb girdle muscular dystrophies
Report one of the more specific codes below.
Codes under this one
- G71.031 Autosomal dominant limb girdle muscular dystrophy
- G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.034 Limb girdle muscular dystrophy due to sarcoglycan dysfunctionHeader
- G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- G71.036 Limb girdle muscular dystrophy due to fukutin related protein dysfunction
- G71.038 Other limb girdle muscular dystrophy
- G71.039 Limb girdle muscular dystrophy, unspecified
Instructional notes
Chapter 6
Excludes2Not included here: the patient may have both; report both when both are present.
- 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)
Chapter 6: Diseases of the nervous system · G70-G73 Diseases of myoneural junction and muscle (G70-G73)
Source: ICD-10-CM FY 2027 code descriptions and tabular list (CMS and CDC National Center for Health Statistics), effective 2026-10-01 through 2027-09-30 · CMS ICD-10 files. HCC mapping: CMS-HCC V28, payment year 2027. As of 2026-11-04.
Coverage and payment depend on the claim details; confirm with the Medicare Administrative Contractor.