Valid for Submission
G24.1 is a billable diagnosis code used to specify a medical diagnosis of genetic torsion dystonia. The code G24.1 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code G24.1 might also be used to specify conditions or terms like autosomal dominant dopa responsive dystonia, autosomal dominant focal dystonia dyt25 type, autosomal dominant idiopathic familial dystonia, autosomal recessive dopa responsive dystonia, autosomal recessive idiopathic familial dystonia , deafness-dystonia-optic neuronopathy syndrome, etc.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code G24.1:
Inclusion TermsInclusion Terms
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.
- Dystonia deformans progressiva
- Dystonia musculorum deformans
- Familial torsion dystonia
- Idiopathic familial dystonia
- Idiopathic (torsion) dystonia NOS
- (Schwalbe-) Ziehen-Oppenheim disease
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code G24.1 are found in the index:
- - Dystonia - G24.9
- - Schwalbe-Ziehen-Oppenheim disease - G24.1
- - Tortipelvis - G24.1
- - Ziehen-Oppenheim disease - G24.1
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Autosomal dominant dopa responsive dystonia
- Autosomal dominant focal dystonia DYT25 type
- Autosomal dominant idiopathic familial dystonia
- Autosomal recessive dopa responsive dystonia
- Autosomal recessive idiopathic familial dystonia
- Deafness-dystonia-optic neuronopathy syndrome
- Disorder of manganese metabolism
- Diurnal dystonia
- Diurnal dystonia
- Dystonia 6
- Dystonia aphonia syndrome
- Generalized dystonia
- Hypermanganesemia with dystonia
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis
- Idiopathic familial dystonia
- Maternally inherited mitochondrial dystonia
- Partington syndrome
- Primary dystonia DYT17 type
- Primary dystonia type 4
- Primary torsion dystonia
- Torsion dystonia
Convert G24.1 to ICD-9 Code
Information for Patients
Dystonia is a movement disorder that causes involuntary contractions of your muscles. These contractions result in twisting and repetitive movements. Sometimes they are painful.
Dystonia can affect just one muscle, a group of muscles or all of your muscles. Symptoms can include tremors, voice problems or a dragging foot. Symptoms often start in childhood. They can also start in the late teens or early adulthood. Some cases worsen over time. Others are mild.
Some people inherit dystonia. Others have it because of another disease. Researchers think that dystonia may be due to a problem in the part of the brain that handles messages about muscle contractions. There is no cure. Doctors use medicines, Botox injections, surgery, physical therapy, and other treatments to reduce or eliminate muscle spasms and pain.
NIH: National Institute of Neurological Disorders and Stroke
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Dystonia 6 Dystonia 6 is one of many forms of dystonia, which is a group of conditions characterized by involuntary movements, twisting (torsion) and tensing of various muscles, and unusual positioning of affected body parts. Dystonia 6 can appear at any age from childhood through adulthood; the average age of onset is 18.The signs and symptoms of dystonia 6 vary among affected individuals. The disorder usually first impacts muscles of the head and neck, causing problems with speaking (dysarthria) and eating (dysphagia). Eyelid twitching (blepharospasm) may also occur. Involvement of one or more limbs is common, and in some cases occurs before the head and neck problems. Dystonia 6 gradually gets worse, and it may eventually involve most of the body.
Early-onset primary dystonia Early-onset primary dystonia is a condition characterized by progressive problems with movement, typically beginning in childhood. Dystonia is a movement disorder that involves involuntary tensing of the muscles (muscle contractions), twisting of specific body parts such as an arm or a leg, rhythmic shaking (tremors), and other uncontrolled movements. A primary dystonia is one that occurs without other neurological symptoms, such as seizures or a loss of intellectual function (dementia). Early-onset primary dystonia does not affect a person's intelligence.On average, the signs and symptoms of early-onset primary dystonia appear around age 12. Abnormal muscle spasms in an arm or a leg are usually the first sign. These unusual movements initially occur while a person is doing a specific action, such as writing or walking. In some affected people, dystonia later spreads to other parts of the body and may occur at rest. The abnormal movements persist throughout life, but they do not usually cause pain.The signs and symptoms of early-onset primary dystonia vary from person to person, even among affected members of the same family. The mildest cases affect only a single part of the body, causing isolated problems such as a writer's cramp in the hand. Severe cases involve abnormal movements affecting many regions of the body.