2026 ICD-10-CM Diagnosis Code G73.7Myopathy in diseases classified elsewhere

ICD-10-CM CodesG00–G99G70-G73G73

ICD-10-CM G73.7
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

G73.7 is a billable ICD-10-CM diagnosis code for myopathy in diseases classified elsewhere. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). The code is a manifestation code that cannot be reported as the principal diagnosis. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Myopathies.

Code Identity

ICD-10-CM Code
G73.7
Billable Status
Yes — Valid for Submission
Code Describes
Myopathy in diseases classified elsewhere
Short Description
Myopathy in diseases classified elsewhere
Same as the full description in the CMS dataset.
Parent Code
Disorders of myoneural junction and muscle in diseases classified elsewhere

Code Classification

ChapterG00–G99Diseases of the nervous system
SectionG70-G73Diseases of myoneural junction and muscle
CategoryG73Disorders of myoneural junction and muscle in diseases classified elsewhere
This CodeG73.7Myopathy in diseases classified elsewhere

Code EditsBilling

Medicare Code Editor checks that affect claim validity for G73.7.

Manifestation codes describe the manifestation of an underlying disease, not the disease itself, and therefore should not be used as a principal diagnosis.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Amyloid myopathy
  • Autoimmune inflammation of skeletal muscle
  • Autoimmune necrotizing myopathy
  • Carcinomatous myopathic syndrome
  • Chronic myopathy with hypocalcemia and hypophosphatemia
  • Endocrine myopathy
  • Glycogen storage disease, muscular form
  • Human immunodeficiency virus myopathy
  • Hypothyroid myopathy
  • Idiopathic inflammatory myopathy
  • Lipid storage myopathy
  • Luft's hypermetabolic myopathy
  • Metabolic myopathy
  • Metabolic myopathy due to lactate transporter defect
  • Mitochondrial-lipid-glycogen storage myopathy
  • Myopathy co-occurrent and due to hypercalcemia
  • Myopathy due to calcium deficiency
  • Myopathy due to Cushing's syndrome
  • Myopathy due to magnesium deficiency
  • Myopathy due to paraneoplastic syndrome
  • Myopathy due to polyarteritis nodosa
  • Myopathy in acromegaly
  • Myopathy in Addison's disease
  • Myopathy in Cushing's disease
  • Myopathy in hyperparathyroidism
  • Myopathy in hypoparathyroidism
  • Myopathy in hypopituitarism
  • Myopathy in myasthenia gravis
  • Myopathy in osteomalacia
  • Neutral lipid storage disease with myopathy
  • Nutritional myopathy
  • Polyglucosan body myopathy type 1
  • Polyglucosan body myopathy type 2
  • Potassium depletion myopathy
  • Primary familial amyloid myopathy
  • Primary sporadic amyloid myopathy
  • Protein deficiency myopathy
  • Secondary myopathy
  • Thyrotoxic myopathy

Tabular List NotesGuidance

Coding notes and annotation back-references applicable to this code.

Code First

  • underlying disease, such as:
  • glycogen storage disease E74.0
  • hyperparathyroidism E21.0 E21.3
  • hypoparathyroidism E20
  • lipid storage disorders E75

Type 1 Excludes

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR NVS018
Myopathies
Default principal diagnosis: inpatient No · outpatient No

Clinical InformationClinical

  • Metabolic Myopathy

    a group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. the disorders are characterized by muscle dysfunction.

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 G73.7 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
359.5 Myopathy in endocrin dis
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About G73.7Overview

Is G73.7 a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report myopathy in diseases classified elsewhere on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

Can G73.7 be a principal diagnosis?

No. This is a manifestation code: myopathy in diseases classified elsewhere describes the manifestation of an underlying disease rather than the disease itself, so the underlying condition is sequenced first.

What is the ICD-9 equivalent of G73.7?

Under the General Equivalence Mappings, myopathy in diseases classified elsewhere converts to ICD-9-CM 359.5 (myopathy in endocrin dis). 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.