G72.89
BillableOther specified myopathies
Other specified myopathies
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
Related Codes(1)
Also Known As / Clinical Terms(55)
SNOMED CT
- Juvenile myopathy AND lactate acidosis4477007
- Fingerprint myopathy23820006
- Proximal myopathy193255007
- Myopathy with cytoplasmic inclusions240086009
- Complication due to and following neuromuscular block397785000
- Neuromuscular block problem397785000
- Hereditary myopathy with lactic acidosis699268002
- Myoglobinuria due to abnormal glycolysis699268002
- Myopathy with deficiency of iron-sulfur cluster assembly enzyme699268002
- Myopathy with deficiency of iron-sulphur cluster assembly enzyme699268002
- Myopathy with deficiency of succinate dehydrogenase and aconitase699268002
- Myopathy with exercise intolerance, Swedish type699268002
- Myofibrillar myopathy699269005
- Distal myopathy with rimmed vacuoles702382000
- Hereditary inclusion body myopathy702382000
- Inclusion body myopathy 2702382000
- Nonaka myopathy702382000
- Quadricep sparing inclusion body myopathy702382000
- Rimmed vacuole myopathy702382000
- Brody disease703530005
- Brody myopathy703530005
- Spheroid body myopathy765092004
- Distal myotilinopathy765196004
- Muscle paresis due to and following neuromuscular blockade823018004
- Muscle weakness due to and following neuromuscular blockade823018004
- Muscle paralysis due to and following neuromuscular blockade823019007
- Proximal myopathy with focal depletion of mitochondria1197756002
Clinical Terms
- Proximal myopathy with focal depletion of mitochondria
- Complication due to and following neuromuscular block
- Fingerprint myopathy
- Quadricep sparing inclusion body myopathy
- Muscle weakness due to and following neuromuscular blockade
- Myopathy with deficiency of succinate dehydrogenase and aconitase
- Rimmed vacuole myopathy
- Myopathy with cytoplasmic inclusions
- Nonaka myopathy
- Distal myotilinopathy
- Muscle paresis due to and following neuromuscular blockade
- Hereditary myopathy with lactic acidosis
- Distal myopathy with rimmed vacuoles
- Myopathy with deficiency of iron-sulfur cluster assembly enzyme
- Spheroid body myopathy
- Hereditary inclusion body myopathy
- Neuromuscular block problem
- Muscle paralysis due to and following neuromuscular blockade
- Myopathy with deficiency of iron-sulphur cluster assembly enzyme
- Juvenile myopathy AND lactate acidosis
- Myofibrillar myopathy
- Brody myopathy
- Inclusion body myopathy 2
- Myopathy with exercise intolerance, Swedish type
- Proximal myopathy
- Myoglobinuria due to abnormal glycolysis
- Brody disease
Frequently Asked Questions
What is the ICD-10 code for other specified myopathies?
The ICD-10-CM code for other specified myopathies is G72.89. The full clinical description is "Other specified myopathies". G72.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G72.89 mean?
ICD-10-CM code G72.89 represents “Other specified myopathies”. 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 G72.89 a billable code?
Yes, G72.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G72.89 in?
G72.89 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G72.89?
G72.89 has Excludes1 notes indicating codes that cannot be used together with it, including: arthrogryposis multiplex congenita (Q74.3); dermatopolymyositis (M33.-); ischemic infarction of muscle (M62.2-); and 2 more.
What SNOMED CT codes does G72.89 map to?
G72.89 maps to 14 SNOMED CT concepts: 703530005, 397785000, 702382000, 765196004, 23820006, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G72.89?
G72.89 is linked to 1 UMLS Concept Unique Identifier: C0477405. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G72.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified myopathies 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 G72.89?
There is no direct ICD-11 mapping available for G72.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.