2026 ICD-10-CM Diagnosis Code G72.89Other specified myopathies
ICD-10-CM Codes›G00–G99›G70-G73›G72
- Billable — Valid for Submission
- Not Chronic
G72.89 is a billable ICD-10-CM diagnosis code for other specified myopathies. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Myopathies.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Brody myopathy
- Complication due to and following neuromuscular block
- Distal myotilinopathy
- Fingerprint myopathy
- Inclusion body myopathy 2
- Juvenile myopathy AND lactate acidosis
- Muscle paralysis due to and following neuromuscular blockade
- Muscle paresis due to and following neuromuscular blockade
- Myofibrillar myopathy
- Myopathy with cytoplasmic inclusions
- Myopathy with deficiency of iron-sulfur cluster assembly enzyme
- Proximal myopathy
- Proximal myopathy with focal depletion of mitochondria
- Spheroid body myopathy
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- progressive NEC - G72.89
- specified NEC - G72.89
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Myopathy
- progressive NEC
- Myopathy
- specified NEC
- Paralysis, paralytic(complete) (incomplete)
- muscle, muscular NEC
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Myofibrillar Myopathy
an inherited or sporadic disorder affecting the skeletal muscles.Myofibrillar Myopathy 1|MFM1
a subtype of myofibrillar myopathy caused by mutations in the des gene, encoding desmin.Myofibrillar Myopathy 2|MFM2
an autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the cryab gene, encoding alpha-crystallin b chain.Myofibrillar Myopathy 3|MFM3
an autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the myot gene, encoding myotilin.Myofibrillar Myopathy 5|MFM5
an autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the flnc gene, encoding filamin-c.Myofibrillar Myopathy 6|BAG3-Related Myofibrillar Myopathy|MFM6|Muscular Dystrophy, Selcen Type
an autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the bag3 gene, encoding bag family molecular chaperone regulator 3.
Patient EducationClinical
Muscle Disorders
Your muscles help you move and help your body work. Different types of muscles have different jobs. There are many problems that can affect muscles. Muscle disorders can cause weakness, pain or even paralysis.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert G72.89 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About G72.89Overview
Is G72.89 (Other specified myopathies) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other specified myopathies on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What is the ICD-9 equivalent of G72.89?
Under the General Equivalence Mappings, other specified myopathies converts to ICD-9-CM 359.89 (myopathies NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.
