ICD-10-CM Diagnosis Code (2025)
Official Description for G72
Other and unspecified myopathies
Coding Notes & Guidelines for G72
- arthrogryposis multiplex congenita (Q74.3)
- dermatopolymyositis (M33.-)
- ischemic infarction of muscle (M62.2-)
- myositis (M60.-)
- polymyositis (M33.2.-)
paramyotonia congenita (of von Eulenburg) (G71.19)
(T51-T65) to identify toxic agent
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
code to identify alcoholism (F10.-)
- Familial periodic paralysis
- Hyperkalemic periodic paralysis (familial)
- Hypokalemic periodic paralysis (familial)
- Myotonic periodic paralysis (familial)
- Normokalemic paralysis (familial)
- Potassium sensitive periodic paralysis
Inflammatory myopathy NOS
- Acute necrotizing myopathy
- Acute quadriplegic myopathy
- Intensive care (ICU) myopathy
- Myopathy of critical illness
Child Codes (More Specific Codes for G72):
About ICD-10-CM Code G72 (Other and unspecified myopathies)
ICD-10-CM code G72 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 G72 became effective on October 1, 2024.
This page provides detailed information about G72 - Other and unspecified 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 Other and unspecified myopathies.