G71.20 Congenital myopathy, unspecified
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Congenital myopathy, unspecified | yes |
Related codes in G71
- G71 Primary disorders of muscles
- G71.0 Muscular dystrophy
- G71.00 Muscular dystrophy, unspecified
- G71.01 Duchenne or Becker muscular dystrophy
- G71.02 Facioscapulohumeral muscular dystrophy
- G71.03 Limb girdle muscular dystrophies
- 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 dysfunction
- G71.0340 Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
- G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- 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
- G71.09 Other specified muscular dystrophies
- G71.1 Myotonic disorders