G73.7
BillableMyopathy in diseases classified elsewhere
Myopathy in diseases classified elsewhere
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Code First
The underlying condition must be sequenced before this code
- underlying disease, such as:
- •glycogen storage diseaseE74.0
- •hyperparathyroidism,E21.0, E21.3
- •hypoparathyroidismE20
- •lipid storage disordersE75
Related Codes(2)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(133)
SNOMED CT
- Myopathy in hypopituitarism14289006
- Glycogen storage disease, muscular form15978003
- Metabolic myopathy26111005
- Myopathy in metabolic diseases26111005
- Myopathy in Addison disease34253008
- Myopathy in Addison's disease34253008
- Mitochondrial-lipid-glycogen storage myopathy37934003
- Nutritional myopathy44253006
- Myopathy in Cushing disease53509000
- Myopathy in Cushing's disease53509000
- Endocrine myopathy57958006
- Muscle disease related to endocrine disease57958006
- Muscle disorders associated with endocrine disease57958006
- Secondary myopathy60738003
- Luft hypermetabolic myopathy62266001
- Luft's hypermetabolic myopathy62266001
- Myopathy due to thyrotoxicosis68437005
- Thyrotoxic myopathy68437005
- Carcinomatous myopathic syndrome71985006
- Myopathy associated with malignant disease71985006
- Hypothyroid myopathy87844004
- Myxedema myopathy87844004
- Myxoedema myopathy87844004
- Amyloid myopathy193247000
- Myopathy due to polyarteritis nodosa193249002
- Myasthenic myopathy230687001
- Myopathy in myasthenia gravis230687001
- Primary familial amyloid myopathy237873000
- Primary sporadic amyloid myopathy237874006
- Myopathy in acromegaly240089002
- Myopathy in hyperparathyroidism240090006
- Myopathy in hypoparathyroidism240091005
- Myopathy in osteomalacia240092003
- Lipid storage myopathy240095001
- Protein deficiency myopathy240098004
- Potassium depletion myopathy240099007
- HIV - Human immunodeficiency virus myopathy240103002
- Human immunodeficiency virus myopathy240103002
- Chronic myopathy with hypocalcaemia and hypophosphataemia277939004
- Chronic myopathy with hypocalcemia and hypophosphatemia277939004
- Autoimmune inflammation of skeletal muscle443899007
- Autoimmune myositis443899007
- Neutral lipid storage disease with myopathy699315005
- Neutral lipid storage disease without ichthyosis699315005
- Idiopathic inflammatory myopathy702380008
- Idiopathic inflammatory myositis702380008
- Autoimmune necrotising myopathy715863001
- Autoimmune necrotizing myopathy715863001
- Immune mediated necrotising myopathy715863001
- Immune mediated necrotizing myopathy715863001
- Myopathy due to magnesium deficiency721190004
- Myopathy co-occurrent and due to hypercalcaemia724559006
- Myopathy co-occurrent and due to hypercalcemia724559006
- Myopathy with hypercalcaemia724559006
- Myopathy with hypercalcemia724559006
- Erythrocyte lactate transporter defect766715000
- Metabolic myopathy due to lactate transporter defect766715000
- PGBM1 - polyglucosan body myopathy type 1774148007
- Polyglucosan body myopathy type 1774148007
- Myopathy due to calcium deficiency870299000
- PGBM2 - polyglucosan body myopathy type 21228849007
- Polyglucosan body myopathy type 21228849007
- Disorder of muscle due to paraneoplastic syndrome1263499004
- Myopathy due to paraneoplastic syndrome1263499004
- Paraneoplastic myopathy1263499004
- Myopathy due to Cushing's syndrome229221000119103
Clinical Terms
- Autoimmune inflammation of skeletal muscle
- Immune mediated necrotizing myopathy
- Myasthenic myopathy
- Myopathy due to polyarteritis nodosa
- Myxedema myopathy
- Primary familial amyloid myopathy
- Mitochondrial-lipid-glycogen storage myopathy
- Myopathy in osteomalacia
- Endocrine myopathy
- Myopathy due to magnesium deficiency
- Neutral lipid storage disease without ichthyosis
- Myopathy with hypercalcemia
- Nutritional myopathy
- Myopathy in Cushing disease
- Myopathy in myasthenia gravis
- Idiopathic inflammatory myositis
- Muscle disorders associated with endocrine disease
- Myopathy co-occurrent and due to hypercalcemia
- Disorder of muscle due to paraneoplastic syndrome
- Immune mediated necrotising myopathy
- Autoimmune myositis
- Glycogen storage disease, muscular form
- Luft's hypermetabolic myopathy
- Potassium depletion myopathy
- Myxoedema myopathy
- Myopathy in hyperparathyroidism
- Protein deficiency myopathy
- Metabolic myopathy
- Polyglucosan body myopathy type 2
- Lipid storage myopathy
- Thyrotoxic myopathy
- Metabolic myopathy due to lactate transporter defect
- Myopathy associated with malignant disease
- Muscle disease related to endocrine disease
- PGBM1 - polyglucosan body myopathy type 1
- Erythrocyte lactate transporter defect
- Paraneoplastic myopathy
- Neutral lipid storage disease with myopathy
- Secondary myopathy
- Carcinomatous myopathic syndrome
- Hypothyroid myopathy
- HIV - Human immunodeficiency virus myopathy
- Amyloid myopathy
- Luft hypermetabolic myopathy
- Myopathy in hypopituitarism
- Idiopathic inflammatory myopathy
- Myopathy due to calcium deficiency
- Myopathy in Cushing's disease
- Myopathy co-occurrent and due to hypercalcaemia
- Chronic myopathy with hypocalcaemia and hypophosphataemia
- Myopathy due to paraneoplastic syndrome
- Primary sporadic amyloid myopathy
- Myopathy in metabolic diseases
- Myopathy in acromegaly
- Human immunodeficiency virus myopathy
- Chronic myopathy with hypocalcemia and hypophosphatemia
- Autoimmune necrotising myopathy
- Autoimmune necrotizing myopathy
- Myopathy with hypercalcaemia
- Myopathy in Addison's disease
- Myopathy in Addison disease
- PGBM2 - polyglucosan body myopathy type 2
- Polyglucosan body myopathy type 1
- Myopathy due to thyrotoxicosis
- Myopathy in hypoparathyroidism
- Myopathy due to Cushing's syndrome
Frequently Asked Questions
What is the ICD-10 code for myopathy in diseases classified elsewhere?
The ICD-10-CM code for myopathy in diseases classified elsewhere is G73.7. The full clinical description is "Myopathy in diseases classified elsewhere". G73.7 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G73.7 mean?
ICD-10-CM code G73.7 represents “Myopathy in diseases classified elsewhere”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G73.7 a billable code?
Yes, G73.7 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G73.7 in?
G73.7 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G73.7?
G73.7 has Excludes1 notes indicating codes that cannot be used together with it, including: myopathy in:; rheumatoid arthritis (M05.32); sarcoidosis (D86.87); and 3 more.
What SNOMED CT codes does G73.7 map to?
G73.7 maps to 39 SNOMED CT concepts: 193247000, 443899007, 715863001, 71985006, 277939004, and 34 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G73.7?
G73.7 is linked to 1 UMLS Concept Unique Identifier: C2875322. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G73.7 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myopathy in diseases classified elsewhere affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G73.7?
G73.7 maps to the ICD-11 code: 8D0Z (Diseases of neuromuscular junction or muscle, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.