G71.29ICD-10-CM 2027 · Billable
Other congenital myopathy
Sibling codes
Inclusion terms
- Central core disease
- Minicore disease
- Multicore disease
- Multiminicore disease
Inherited from G71.2: Congenital myopathies
Excludes2
- arthrogryposis multiplex congenita (
Q74.3)
Inherited from G71: Primary disorders of muscles
Excludes2
Part of: G71.2: Congenital myopathies › G71: Primary disorders of muscles