ICD-10-CM Diagnosis Code (2025)
Official Description for G71.2
Congenital myopathies
Coding Notes & Guidelines for G71.2
Excludes2: Not Included Here
arthrogryposis multiplex congenita (Q74.3)
Inclusion Terms
Myotubular (centronuclear) myopathy
Inclusion Terms
- Autosomal centronuclear myopathy
- Autosomal dominant centronuclear myopathy
- Autosomal recessive centronuclear myopathy
- Centronuclear myopathy, NOS
Inclusion Terms
- Central core disease
- Minicore disease
- Multicore disease
- Multiminicore disease
Parent Code (Less Specific):
About ICD-10-CM Code G71.2 (Congenital myopathies)
ICD-10-CM code G71.2 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM G71.2 became effective on October 1, 2024.
This page provides detailed information about G71.2 - Congenital myopathies. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Congenital myopathies.