• Myopathy G72.9
    ICD-10-CM Diagnosis Code G72.9

    Myopathy, unspecified

      2016 2017 2018 2019 Billable/Specific Code

    • acute
      • necrotizing G72.81
        ICD-10-CM Diagnosis Code G72.81

        Critical illness myopathy

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Acute necrotizing myopathy
        • Acute quadriplegic myopathy
        • Intensive care (ICU) myopathy
        • Myopathy of critical illness
      • quadriplegic G72.81
        ICD-10-CM Diagnosis Code G72.81

        Critical illness myopathy

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Acute necrotizing myopathy
        • Acute quadriplegic myopathy
        • Intensive care (ICU) myopathy
        • Myopathy of critical illness
    • alcoholic G72.1
      ICD-10-CM Diagnosis Code G72.1

      Alcoholic myopathy

        2016 2017 2018 2019 Billable/Specific Code
      Use Additional
      • code to identify alcoholism (F10.-)
    • benign congenital G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • central core G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • centronuclear G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • congenital G71.2
      (benign)
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • critical illness G72.81
      ICD-10-CM Diagnosis Code G72.81

      Critical illness myopathy

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Acute necrotizing myopathy
      • Acute quadriplegic myopathy
      • Intensive care (ICU) myopathy
      • Myopathy of critical illness
    • distal G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

        2019 - New Code Billable/Specific Code
      Applicable To
      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Limb-girdle muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • drug-induced G72.0
      ICD-10-CM Diagnosis Code G72.0

      Drug-induced myopathy

        2016 2017 2018 2019 Billable/Specific Code
      Use Additional
      • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
    • endocrine NEC E34.9
      ICD-10-CM Diagnosis Code E34.9

      Endocrine disorder, unspecified

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Endocrine disturbance NOS
      • Hormone disturbance NOS
    • extraocular muscles H05.82-
      ICD-10-CM Diagnosis Code H05.82-

      Myopathy of extraocular muscles

        2016 2017 2018 2019 Non-Billable/Non-Specific Code
    • facioscapulohumeral G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

        2019 - New Code Billable/Specific Code
      Applicable To
      • Scapulohumeral muscular dystrophy
    • hereditary G71.9
      ICD-10-CM Diagnosis Code G71.9

      Primary disorder of muscle, unspecified

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Hereditary myopathy NOS
      • specified NEC G71.8
        ICD-10-CM Diagnosis Code G71.8

        Other primary disorders of muscles

          2016 2017 2018 2019 Billable/Specific Code
    • immune NEC G72.49
      ICD-10-CM Diagnosis Code G72.49

      Other inflammatory and immune myopathies, not elsewhere classified

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Inflammatory myopathy NOS
    • in (due to)
      • Addison's disease E27.1
        ICD-10-CM Diagnosis Code E27.1

        Primary adrenocortical insufficiency

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Addison's disease
        • Autoimmune adrenalitis
        Type 1 Excludes
        • Addison only phenotype adrenoleukodystrophy (E71.528)
        • amyloidosis (E85.-)
        • tuberculous Addison's disease (A18.7)
        • Waterhouse-Friderichsen syndrome (A39.1)
      • alcohol G72.1
        ICD-10-CM Diagnosis Code G72.1

        Alcoholic myopathy

          2016 2017 2018 2019 Billable/Specific Code
        Use Additional
        • code to identify alcoholism (F10.-)
      • amyloidosis E85.0
        ICD-10-CM Diagnosis Code E85.0

        Non-neuropathic heredofamilial amyloidosis

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Hereditary amyloid nephropathy
        Code Also
        • associated disorders, such as:
        • autoinflammatory syndromes (M04.-)
        Type 2 Excludes
        • Transthyretin-related (ATTR) familial amyloid cardiomyopathy (E85.4)
      • cretinism E00.9
        ICD-10-CM Diagnosis Code E00.9

        Congenital iodine-deficiency syndrome, unspecified

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Congenital iodine-deficiency hypothyroidism NOS
        • Endemic cretinism NOS
      • Cushing's syndrome E24.9
        ICD-10-CM Diagnosis Code E24.9

        Cushing's syndrome, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • drugs G72.0
        ICD-10-CM Diagnosis Code G72.0

        Drug-induced myopathy

          2016 2017 2018 2019 Billable/Specific Code
        Use Additional
        • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
      • endocrine disease NEC E34.9
        ICD-10-CM Diagnosis Code E34.9

        Endocrine disorder, unspecified

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Endocrine disturbance NOS
        • Hormone disturbance NOS
      • giant cell arteritis M31.6
        ICD-10-CM Diagnosis Code M31.6

        Other giant cell arteritis

          2016 2017 2018 2019 Billable/Specific Code
      • glycogen storage disease E74.00
        ICD-10-CM Diagnosis Code E74.00

        Glycogen storage disease, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • hyperadrenocorticism E24.9
        ICD-10-CM Diagnosis Code E24.9

        Cushing's syndrome, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • hyperparathyroidism NEC E21.3
        ICD-10-CM Diagnosis Code E21.3

        Hyperparathyroidism, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • hypoparathyroidism E20.9
        ICD-10-CM Diagnosis Code E20.9

        Hypoparathyroidism, unspecified

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Parathyroid tetany
      • hypopituitarism E23.0
        ICD-10-CM Diagnosis Code E23.0

        Hypopituitarism

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Fertile eunuch syndrome
        • Hypogonadotropic hypogonadism
        • Idiopathic growth hormone deficiency
        • Isolated deficiency of gonadotropin
        • Isolated deficiency of growth hormone
        • Isolated deficiency of pituitary hormone
        • Kallmann's syndrome
        • Lorain-Levi short stature
        • Necrosis of pituitary gland (postpartum)
        • Panhypopituitarism
        • Pituitary cachexia
        • Pituitary insufficiency NOS
        • Pituitary short stature
        • Sheehan's syndrome
        • Simmonds' disease
      • hypothyroidism E03.9
        ICD-10-CM Diagnosis Code E03.9

        Hypothyroidism, unspecified

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Myxedema NOS
      • infectious disease NEC B99
        ICD-10-CM Diagnosis Code B99

        Other and unspecified infectious diseases

          2016 2017 2018 2019 Non-Billable/Non-Specific Code
      • lipid storage disease E75.6
        ICD-10-CM Diagnosis Code E75.6

        Lipid storage disorder, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • metabolic disease NEC E88.9
        ICD-10-CM Diagnosis Code E88.9

        Metabolic disorder, unspecified

          2016 2017 2018 2019 Billable/Specific Code
      • myxedema E03.9
        ICD-10-CM Diagnosis Code E03.9

        Hypothyroidism, unspecified

          2016 2017 2018 2019 Billable/Specific Code
        Applicable To
        • Myxedema NOS
      • parasitic disease NEC B89
        ICD-10-CM Diagnosis Code B89

        Unspecified parasitic disease

          2016 2017 2018 2019 Billable/Specific Code
      • polyarteritis nodosa M30.0
        ICD-10-CM Diagnosis Code M30.0

        Polyarteritis nodosa

          2016 2017 2018 2019 Billable/Specific Code
      • rheumatoid arthritis - see Rheumatoid, myopathy
      • sarcoidosis D86.87
        ICD-10-CM Diagnosis Code D86.87

        Sarcoid myositis

          2016 2017 2018 2019 Billable/Specific Code
      • scleroderma M34.82
        ICD-10-CM Diagnosis Code M34.82

        Systemic sclerosis with myopathy

          2016 2017 2018 2019 Billable/Specific Code
      • sicca syndrome M35.03
        ICD-10-CM Diagnosis Code M35.03

        Sicca syndrome with myopathy

          2016 2017 2018 2019 Billable/Specific Code
      • Sjögren's syndrome M35.03
        ICD-10-CM Diagnosis Code M35.03

        Sicca syndrome with myopathy

          2016 2017 2018 2019 Billable/Specific Code
      • systemic lupus erythematosus M32.19
        ICD-10-CM Diagnosis Code M32.19

        Other organ or system involvement in systemic lupus erythematosus

          2016 2017 2018 2019 Billable/Specific Code
      • thyrotoxicosis (hyperthyroidism) E05.90
        ICD-10-CM Diagnosis Code E05.90

        Thyrotoxicosis, unspecified without thyrotoxic crisis or storm

          2016 2017 2018 2019 Billable/Specific Code
        • with thyroid storm E05.91
          ICD-10-CM Diagnosis Code E05.91

          Thyrotoxicosis, unspecified with thyrotoxic crisis or storm

            2016 2017 2018 2019 Billable/Specific Code
      • toxic agent NEC G72.2
        ICD-10-CM Diagnosis Code G72.2

        Myopathy due to other toxic agents

          2016 2017 2018 2019 Billable/Specific Code
        Code First
    • inflammatory NEC G72.49
      ICD-10-CM Diagnosis Code G72.49

      Other inflammatory and immune myopathies, not elsewhere classified

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Inflammatory myopathy NOS
    • intensive care G72.81
      (ICU)
      ICD-10-CM Diagnosis Code G72.81

      Critical illness myopathy

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Acute necrotizing myopathy
      • Acute quadriplegic myopathy
      • Intensive care (ICU) myopathy
      • Myopathy of critical illness
    • limb-girdle G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

        2019 - New Code Billable/Specific Code
      Applicable To
      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Limb-girdle muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • mitochondrial NEC G71.3
      ICD-10-CM Diagnosis Code G71.3

      Mitochondrial myopathy, not elsewhere classified

        2016 2017 2018 2019 Billable/Specific Code
      Type 1 Excludes
      • Kearns-Sayre syndrome (H49.81)
      • Leber's disease (H47.21)
      • Leigh's encephalopathy (G31.82)
      • mitochondrial metabolism disorders (E88.4.-)
      • Reye's syndrome (G93.7)
    • myotubular G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • mytonic, proximal G71.11
      (PROMM)
      ICD-10-CM Diagnosis Code G71.11

      Myotonic muscular dystrophy

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Dystrophia myotonica [Steinert]
      • Myotonia atrophica
      • Myotonic dystrophy
      • Proximal myotonic myopathy (PROMM)
      • Steinert disease
    • nemaline G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • ocular G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

        2019 - New Code Billable/Specific Code
      Applicable To
      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Limb-girdle muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • oculopharyngeal G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

        2019 - New Code Billable/Specific Code
      Applicable To
      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Limb-girdle muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • of critical illness G72.81
      ICD-10-CM Diagnosis Code G72.81

      Critical illness myopathy

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Acute necrotizing myopathy
      • Acute quadriplegic myopathy
      • Intensive care (ICU) myopathy
      • Myopathy of critical illness
    • primary G71.9
      ICD-10-CM Diagnosis Code G71.9

      Primary disorder of muscle, unspecified

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Hereditary myopathy NOS
      • specified NEC G71.8
        ICD-10-CM Diagnosis Code G71.8

        Other primary disorders of muscles

          2016 2017 2018 2019 Billable/Specific Code
    • progressive NEC G72.89
      ICD-10-CM Diagnosis Code G72.89

      Other specified myopathies

        2016 2017 2018 2019 Billable/Specific Code
    • proximal myotonic G71.11
      (PROMM)
      ICD-10-CM Diagnosis Code G71.11

      Myotonic muscular dystrophy

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Dystrophia myotonica [Steinert]
      • Myotonia atrophica
      • Myotonic dystrophy
      • Proximal myotonic myopathy (PROMM)
      • Steinert disease
    • rod G71.2
      ICD-10-CM Diagnosis Code G71.2

      Congenital myopathies

        2016 2017 2018 2019 Billable/Specific Code
      Applicable To
      • Central core disease
      • Fiber-type disproportion
      • Minicore disease
      • Multicore disease
      • Myotubular (centronuclear) myopathy
      • Nemaline myopathy
      Type 1 Excludes
      • arthrogryposis multiplex congenita (Q74.3)
    • scapulohumeral G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

        2019 - New Code Billable/Specific Code
      Applicable To
      • Scapulohumeral muscular dystrophy
    • specified NEC G72.89
      ICD-10-CM Diagnosis Code G72.89

      Other specified myopathies

        2016 2017 2018 2019 Billable/Specific Code
    • toxic G72.2
      ICD-10-CM Diagnosis Code G72.2

      Myopathy due to other toxic agents

        2016 2017 2018 2019 Billable/Specific Code
      Code First