G71.0
Muscular dystrophy
Coding guidance (WHO 2019)
Muscular dystrophy: autosomal recessive, childhood type, resembling Duchenne or Becker benign [Becker] benign scapuloperoneal with early contractures [Emery-Dreifuss] distal facioscapulohumeral limb-girdle ocular oculopharyngeal scapuloperoneal severe [Duchenne] Excl.: congenital muscular dystrophy: NOS (G71.2) with specific morphological abnormalities of the muscle fibre (G71.2)