8A02.12 Dystonia associated with heredodegenerative disorders
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Dystonia associated with heredodegenerative disorders
- Dystonia due to autosomal dominant disorders
- Rapid-onset dystonia-parkinsonism
- Dystonia due to dentatorubropallidoluysian atrophy
- Dystonia due to Huntington disease
- Dystonia due to autosomal recessive disorders
- Dystonia due to Wilson disease
- Dystonia due to Niemann-Pick disease type C
- Dystonia due to other autosomal recessive metabolic disorders
- Dystonia due to GM2 gangliosidosis
- Dystonia due to Metachromatic leukodystrophy
- Dystonia due to homocystinuria
- Dystonia due to glutaric acidaemia
- Dystonia due to Hartnup disease
- Dystonia due to ataxia-telangiectasia
- Dystonia in neurodegeneration with brain iron accumulation type 1
- NBIA 2 PLA2G6 mutation
- PANK gene mutation
- Dystonia due to Juvenile Parkinson Disease including Parkin mutation
- Probable autosomal recessive dystonia
- Progressive pallidal degeneration
- Dystonia due to X-linked dominant disorders
- Dystonia due to Rett syndrome
- Dystonia due to X-linked recessive disorders
- Deafness-dystonia optic atrophy syndrome
- Mohr-Tranebjærg syndrome
- Dystonia due to Pelizaeus-Merzbacher disease
- Dystonia due to Lesch-Nyhan syndrome
- Dystonia due to mitochondrial cytopathies
- Dystonia due to Leber's disease
- Dystonia due to other mitochondrial cytopathies
- Dystonia of variable inheritance
- Dystonia due to Familial basal ganglia calcifications
- Dystonia due to certain specified inherited disorders
- Dystonia associated with familial basal ganglia calcifications
- Dystonia due to isolated hereditary vitamin E deficiency
- Dystonia due to hereditary spastic paraplegia
- Dystonia 16
- Infantile dystonia-parkinsonism
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