G71.2 – Congenital myopathies
Coding Notes
Removed
Non-billable / Non-specific, not valid for HIPAA-covered transactions
Tyoe 2 Excludes
arthrogryposis multiplex congenita (Q74.3)
GEM Conversion to ICD-9 CM
Fs: 10000
–
Congenital hereditary muscular dystrophy
Child Codes
Sibling Codes
Parent Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| G00-G99 | Diseases of the nervous system (G00-G99) |
| G70-G73 | Diseases of myoneural junction and muscle (G70-G73) |
| G71 | Primary disorders of muscles |
| G71.2 |
Congenital myopathies
Type 2 Excludes
arthrogryposis multiplex congenita (Q74.3)
|
| G71.20 | Congenital myopathy, unspecified |
| G71.21 | Nemaline myopathy |
| G71.22 | Centronuclear myopathy |
| G71.220 | X-linked myotubular myopathy |
| G71.228 | Other centronuclear myopathy |
| G71.29 | Other congenital myopathy |