ICD-10-CM Myopathy References

"Myopathy" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "myopathy"

  • Myopathy - G72.9 Myopathy, unspecified
    • acute
      • necrotizing - G72.81 Critical illness myopathy
      • quadriplegic - G72.81 Critical illness myopathy
    • alcoholic - G72.1 Alcoholic myopathy
    • benign congenital - G71.20 Congenital myopathy, unspecified
    • central core - G71.29 Other congenital myopathy
    • centronuclear - G71.228 Other centronuclear myopathy
      • autosomal (dominant) (recessive) - G71.228 Other centronuclear myopathy
      • other specified NEC - G71.228 Other centronuclear myopathy
    • congenital (benign) - G71.20 Congenital myopathy, unspecified
    • critical illness - G72.81 Critical illness myopathy
    • distal - G71.09 Other specified muscular dystrophies
    • drug-induced - G72.0 Drug-induced myopathy
    • endocrine NEC - E34.9 Endocrine disorder, unspecified
    • extraocular muscles - H05.82 Myopathy of extraocular muscles
    • facioscapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
    • hereditary - G71.9 Primary disorder of muscle, unspecified
      • specified NEC - G71.8 Other primary disorders of muscles
    • hyaline body - G71.29 Other congenital myopathy
    • immune NEC - G72.49 Other inflammatory and immune myopathies, not elsewhere classified
    • in (due to)
      • Addison's disease - E27.1 Primary adrenocortical insufficiency
      • alcohol - G72.1 Alcoholic myopathy
      • amyloidosis - E85.0 Non-neuropathic heredofamilial amyloidosis
      • cretinism - E00.9 Congenital iodine-deficiency syndrome, unspecified
      • Cushing's syndrome - E24.9 Cushing's syndrome, unspecified
      • drugs - G72.0 Drug-induced myopathy
      • endocrine disease NEC - E34.9 Endocrine disorder, unspecified
      • giant cell arteritis - M31.6 Other giant cell arteritis
      • glycogen storage disease - E74.00 Glycogen storage disease, unspecified
      • hyperadrenocorticism - E24.9 Cushing's syndrome, unspecified
      • hyperparathyroidism NEC - E21.3 Hyperparathyroidism, unspecified
      • hypoparathyroidism - E20.9 Hypoparathyroidism, unspecified
      • hypopituitarism - E23.0 Hypopituitarism
      • hypothyroidism - E03.9 Hypothyroidism, unspecified
      • infectious disease NEC - B99 Other and unspecified infectious diseases
      • lipid storage disease - E75.6 Lipid storage disorder, unspecified
      • metabolic disease NEC - E88.9 Metabolic disorder, unspecified
      • myxedema - E03.9 Hypothyroidism, unspecified
      • parasitic disease NEC - B89 Unspecified parasitic disease
      • polyarteritis nodosa - M30.0 Polyarteritis nodosa
      • rheumatoid arthritis - See: Rheumatoid, myopathy;
      • sarcoidosis - D86.87 Sarcoid myositis
      • scleroderma - M34.82 Systemic sclerosis with myopathy
      • sicca syndrome - M35.03 Sjogren syndrome with myopathy
      • Sjögren's syndrome - M35.03 Sjogren syndrome with myopathy
      • systemic lupus erythematosus - M32.19 Other organ or system involvement in systemic lupus erythematosus
      • thyrotoxicosis (hyperthyroidism) - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
        • with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
      • toxic agent NEC - G72.2 Myopathy due to other toxic agents
    • inflammatory NEC - G72.49 Other inflammatory and immune myopathies, not elsewhere classified
    • intensive care (ICU) - G72.81 Critical illness myopathy
    • limb-girdle - See: Dystrophy, muscular, limb-girdle;
    • mitochondrial NEC - G71.3 Mitochondrial myopathy, not elsewhere classified
    • Miyoshi, type 3 - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
    • myosin storage - G71.29 Other congenital myopathy
    • myotubular (centronuclear) - G71.220 X-linked myotubular myopathy
      • X-linked - G71.220 X-linked myotubular myopathy
    • mytonic, proximal (PROMM) - G71.11 Myotonic muscular dystrophy
    • nemaline - G71.21 Nemaline myopathy
    • ocular - G71.09 Other specified muscular dystrophies
    • oculopharyngeal - G71.09 Other specified muscular dystrophies
    • of critical illness - G72.81 Critical illness myopathy
    • primary - G71.9 Primary disorder of muscle, unspecified
      • specified NEC - G71.8 Other primary disorders of muscles
    • progressive NEC - G72.89 Other specified myopathies
    • proximal myotonic (PROMM) - G71.11 Myotonic muscular dystrophy
    • rod (body) - G71.21 Nemaline myopathy
    • scapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
    • specified NEC - G72.89 Other specified myopathies
    • toxic - G72.2 Myopathy due to other toxic agents

Applicable Clinical Terms Definitions

Alcoholics: Persons who have a history of physical or psychological dependence on ETHANOL.