ICD-10 Diagnosis Code G71.11

Myotonic muscular dystrophy

Diagnosis Code G71.11

ICD-10: G71.11
Short Description: Myotonic muscular dystrophy
Long Description: Myotonic muscular dystrophy
This is the 2018 version of the ICD-10-CM diagnosis code G71.11

Valid for Submission
The code G71.11 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the nervous system (G00–G99)
    • Diseases of myoneural junction and muscle (G70-G73)
      • Primary disorders of muscles (G71)

Information for Medical Professionals

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
  • 359.21 - Myotonic musclr dystrphy

  • Cardiomyopathy in myotonic dystrophy
  • Congenital myotonic dystrophy
  • Dilated cardiomyopathy secondary to muscular dystrophy
  • Dilated cardiomyopathy secondary to myotonic dystrophy
  • Dilated cardiomyopathy secondary to neuromuscular disorder
  • Dystrophia myotonica facies
  • Steinert myotonic dystrophy syndrome

Index of Diseases and Injuries
References found for the code G71.11 in the Index of Diseases and Injuries:

Information for Patients

Muscular Dystrophy

Also called: MD

Muscular dystrophy (MD) is a group of more than 30 inherited diseases. They all cause muscle weakness and muscle loss. Some forms of MD appear in infancy or childhood. Others may not appear until middle age or later. The different types can vary in whom they affect, which muscles they affect, and what the symptoms are. All forms of MD grow worse as the person's muscles get weaker. Most people with MD eventually lose the ability to walk.

There is no cure for muscular dystrophy. Treatments can help with the symptoms and prevent complications. They include physical and speech therapy, orthopedic devices, surgery, and medications. Some people with MD have mild cases that worsen slowly. Others cases are disabling and severe.

NIH: National Institute of Neurological Disorders and Stroke

  • Becker muscular dystrophy (Medical Encyclopedia)
  • Creatine phosphokinase test (Medical Encyclopedia)
  • Duchenne muscular dystrophy (Medical Encyclopedia)
  • Limb-girdle muscular dystrophies (Medical Encyclopedia)
  • Muscular dystrophy (Medical Encyclopedia)

[Read More]

Myotonic dystrophy Myotonic dystrophy is part of a group of inherited disorders called muscular dystrophies. It is the most common form of muscular dystrophy that begins in adulthood.Myotonic dystrophy is characterized by progressive muscle wasting and weakness. People with this disorder often have prolonged muscle contractions (myotonia) and are not able to relax certain muscles after use. For example, a person may have difficulty releasing their grip on a doorknob or handle. Also, affected people may have slurred speech or temporary locking of their jaw.Other signs and symptoms of myotonic dystrophy include clouding of the lens of the eye (cataracts) and abnormalities of the electrical signals that control the heartbeat (cardiac conduction defects). In affected men, hormonal changes may lead to early balding and an inability to father a child (infertility). The features of this disorder often develop during a person's twenties or thirties, although they can occur at any age. The severity of the condition varies widely among affected people, even among members of the same family.There are two major types of myotonic dystrophy: type 1 and type 2. Their signs and symptoms overlap, although type 2 tends to be milder than type 1. The muscle weakness associated with type 1 particularly affects the lower legs, hands, neck, and face. Muscle weakness in type 2 primarily involves the muscles of the neck, shoulders, elbows, and hips. The two types of myotonic dystrophy are caused by mutations in different genes.A variation of type 1 myotonic dystrophy, called congenital myotonic dystrophy, is apparent at birth. Characteristic features include weak muscle tone (hypotonia), an inward- and upward-turning foot (clubfoot), breathing problems, delayed development, and intellectual disability. Some of these health problems can be life-threatening.
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