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Dystonic Disorders MeSH Descriptor Data 2024


MeSH Heading
Dystonic Disorders
Tree Number(s)
C10.228.662.300
Unique ID
D020821
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020821
Annotation
DYSTONIA is also available
Scope Note
Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset.
Entry Version
DYSTONIC DIS
Entry Term(s)
Adult-Onset Dystonias
Adult-Onset Idiopathic Focal Dystonias
Adult-Onset Idiopathic Torsion Dystonias
Autosomal Dominant Familial Dystonia
Autosomal Recessive Familial Dystonia
Childhood Onset Dystonias
Dystonia Disorders
Dystonia, Hereditary
Dystonia, Primary
Dystonia, Psychogenic
Dystonia, Secondary
Dystonias, Sporadic
Familial Dystonia
Familial Dystonia, Autosomal Dominant
Familial Dystonia, Autosomal Recessive
Familial Dystonia, Idiopathic
Focal Dystonia
Pseudodystonia
Secondary Dystonia
Writer's Cramp
Previous Indexing
Dystonia (1966-1999)
See Also
Dystonia
Public MeSH Note
2000
History Note
2000
Date Established
2000/01/01
Date of Entry
1999/11/08
Revision Date
1955/01/01
Dystonic Disorders Preferred
Familial Dystonia Narrower
Focal Dystonia Narrower
Pseudodystonia Narrower
Writer's Cramp Narrower
Adult-Onset Dystonias Narrower
Adult-Onset Idiopathic Focal Dystonias Narrower
Adult-Onset Idiopathic Torsion Dystonias Narrower
Autosomal Dominant Familial Dystonia Narrower
Autosomal Recessive Familial Dystonia Narrower
Childhood Onset Dystonias Narrower
Dystonia, Primary Narrower
Dystonia, Secondary Narrower
Dystonias, Sporadic Narrower
Familial Dystonia, Idiopathic Narrower
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