Myopathy - in the ICD-10-CM Index

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

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