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ALL MEDICAL CODES IN CATEGORY Diseases of myoneural junction and muscle

2025 ICD-10-CM code G71

Primary disorders of muscles

2025 ICD-10-CM code G71.033

Limb-girdle muscular dystrophy due to dysferlin dysfunction.

2025 ICD-10-CM code G71.039

Limb girdle muscular dystrophy, unspecified. This code excludes arthrogryposis multiplex congenita (Q74.3), metabolic disorders (E70-E88), and myositis (M60.-).

2025 ICD-10-CM code G71.038

Other limb girdle muscular dystrophy (LGMD). This includes LGMD R9 (FKRP-related LGMD), R22 (collagen 6-related), Limb girdle muscular dystrophy due to fukutin related protein dysfunction, and Limb girdle muscular dystrophy type 2I.

2025 ICD-10-CM code G71.0

Muscular dystrophy. This is a genetic disorder characterized by progressive muscle weakness and degeneration.

2025 ICD-10-CM code G72.81

Critical illness myopathy (CIM) is a severe muscle weakness occurring in intensive care unit (ICU) patients, often linked to critical illness, muscle relaxants, and corticosteroids.

2025 ICD-10-CM code G70.89

G70.89, Other specified myoneural disorders, refers to a group of neuromuscular conditions not otherwise specified in the ICD-10-CM classification.

2025 ICD-10-CM code G71.11

Myotonic muscular dystrophy, also known as Steinert disease, is an inherited neuromuscular disorder causing progressive muscle weakness and impaired muscle relaxation.

2025 ICD-10-CM code G71.9

Primary disorder of muscle, unspecified. This code is used when the provider doesn't specify the type of muscle disorder, which generally involves muscle weakness and atrophy.

2025 ICD-10-CM code G71.2

Congenital myopathies

2025 ICD-10-CM code G72.3

Periodic paralysis encompasses various forms, including familial, hyperkalemic, hypokalemic, myotonic, and normokalemic paralysis.

2025 ICD-10-CM code G70

Myasthenia gravis and other myoneural disorders

2025 ICD-10-CM code G71.00

Unspecified muscular dystrophy (MD) is a muscle disorder characterized by muscle weakness and contractures due to the lack of dystrophin protein.

2025 ICD-10-CM code G72.8

Other specified myopathies.

2025 ICD-10-CM code G71.031

Autosomal dominant limb girdle muscular dystrophy (LGMD).

2025 ICD-10-CM code G71.09

Other specified muscular dystrophies. This code encompasses muscular dystrophies not classified elsewhere.

2025 ICD-10-CM code G71.01

Duchenne or Becker muscular dystrophy

2025 ICD-10-CM code G70.1

Toxic myoneural disorders. This condition involves muscle weakness due to exposure to toxins.

2025 ICD-10-CM code G72.89

This code represents other specified myopathies, encompassing muscle disorders not otherwise classified.

2025 ICD-10-CM code G70.8

Other specified myoneural disorders.

2025 ICD-10-CM code G72.41

Inclusion body myositis (IBM) is a rare inflammatory and degenerative muscle disorder. It's characterized by progressive weakness, typically affecting distal muscles more than proximal ones.

2025 ICD-10-CM code G71.20

Congenital myopathy, unspecified.

2025 ICD-10-CM code G71.220

X-linked myotubular myopathy. This is a congenital myopathy characterized by muscle weakness and hypotonia.

2025 ICD-10-CM code G71.3

Mitochondrial myopathy, not elsewhere classified.

2025 ICD-10-CM code G72.1

Alcoholic myopathy. Use additional code to identify alcoholism (F10.-).

2025 ICD-10-CM code G71.8

Other primary disorders of muscles. This code is used for primary muscle disorders not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code G71.0349

Limb-girdle muscular dystrophy due to other sarcoglycan dysfunction.

2025 ICD-10-CM code G72.9

Myopathy, unspecified. This code is used when the provider does not specify the type of myopathy present.

2025 ICD-10-CM code G71.0341

Limb-girdle muscular dystrophy due to alpha sarcoglycan dysfunction. Alpha sarcoglycanopathy.

2025 ICD-10-CM code G71.19

Other specified myotonic disorders are a group of neuromuscular disorders characterized by delayed muscle relaxation after contraction.

2025 ICD-10-CM code G71.228

Other centronuclear myopathy. This encompasses various forms like autosomal centronuclear myopathy (dominant and recessive types).

2025 ICD-10-CM code G71.035

Limb-girdle muscular dystrophy due to anoctamin-5 dysfunction.

2025 ICD-10-CM code G71.034

Limb-girdle muscular dystrophy due to sarcoglycan dysfunction.

2025 ICD-10-CM code G70.00

Myasthenia gravis without acute exacerbation. This condition is characterized by muscle weakness and fatigue without respiratory failure.

2025 ICD-10-CM code G73.1

Lambert-Eaton syndrome in neoplastic disease. Code first underlying neoplasm.

2025 ICD-10-CM code G70.0

Myasthenia gravis.

2025 ICD-10-CM code G71.032

Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction. Limb girdle muscular dystrophy type 2A.

2025 ICD-10-CM code G71.03

Limb-girdle muscular dystrophies.

2025 ICD-10-CM code G70.01

Myasthenia gravis with acute exacerbation.

2025 ICD-10-CM code G71.1

Myotonic disorders

2025 ICD-10-CM code G70.9

Myoneural disorder, unspecified.

2025 ICD-10-CM code G72.0

Drug-induced myopathy. Use additional code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5).

2025 ICD-10-CM code G71.0342

Limb-girdle muscular dystrophy due to beta sarcoglycan dysfunction.

2025 ICD-10-CM code G71.13

Myotonic chondrodystrophy, also known as chondrodystrophic myotonia or Schwartz-Jampel syndrome.

2025 ICD-10-CM code G71.21

Nemaline myopathy. A congenital myopathy characterized by the presence of nemaline rods in muscle fibers.

2025 ICD-10-CM code G71.02

Facioscapulohumeral muscular dystrophy. Scapulohumeral muscular dystrophy.

2025 ICD-10-CM code G70.80

Lambert-Eaton syndrome, unspecified. This code is used when the type of Lambert-Eaton myasthenic syndrome (LEMS) is not specified in the documentation.

2025 ICD-10-CM code G71.22

Centronuclear myopathy

2025 ICD-10-CM code G71.12

Myotonia congenita (MC) is a genetic neuromuscular disorder characterized by delayed muscle relaxation after contraction, resulting in muscle stiffness.

2025 ICD-10-CM code G71.0340

Limb-girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified. Sarcoglycanopathy, NOS.

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