Diagnosis Code A81.82
Information for Medical Professionals
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.
- 046.71 - Gerstmn-Straus-Schnk syn
- Gerstmann-Straussler-Scheinker syndrome
- Prion disease
Index of Diseases and Injuries
References found for the code A81.82 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of “other specified” codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- GSS syndrome
Information for Patients
Degenerative Nerve Diseases
Also called: Neurodegenerative diseases
Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. Sometimes the cause is a medical condition such as alcoholism, a tumor, or a stroke. Other causes may include toxins, chemicals, and viruses. Sometimes the cause is not known.
Degenerative nerve diseases include
- Alzheimer's disease
- Amyotrophic lateral sclerosis
- Friedreich's ataxia
- Huntington's disease
- Lewy body disease
- Parkinson's disease
- Spinal muscular atrophy
Degenerative nerve diseases can be serious or life-threatening. It depends on the type. Most of them have no cure. Treatments may help improve symptoms, relieve pain, and increase mobility.
- Multiple system atrophy (Medical Encyclopedia)
- Progressive multifocal leukoencephalopathy (Medical Encyclopedia)
Prion disease Prion disease represents a group of conditions that affect the nervous system in humans and animals. In people, these conditions impair brain function, causing changes in memory, personality, and behavior; a decline in intellectual function (dementia); and abnormal movements, particularly difficulty with coordinating movements (ataxia). The signs and symptoms of prion disease typically begin in adulthood and worsen with time, leading to death within a few months to several years.