Descriptor English: | Myotonic Disorders | ||||||
Descriptor Spanish: |
Trastornos Miotónicos
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Descriptor Portuguese: | Transtornos Miotônicos | ||||||
Descriptor French: | Troubles myotoniques | ||||||
Entry term(s): |
Disorder, Myotonic Disorders, Myotonic Eulenburg Disease Eulenburg's Disease Myopathies, Myotonic Myopathy, Myotonic Myotonia Fluctuans Myotonic Disorder Myotonic Myopathies Myotonic Myopathy Paralysis Periodica Paramyotonia Paramyotonia Congenita Paramyotonia Congenita Without Cold Paralysis Paramyotonia Congenita of von Eulenberg Von Eulenberg Disease Von Eulenberg's Disease |
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Tree number(s): |
C05.651.662 C10.668.491.606 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020967 | ||||||
Scope note: | Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Myotonic Dystrophy (1965-1999) |
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Public MeSH Note: | 2000 |
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History Note: | 2000 |
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Entry Version: | MYOTONIC DIS |
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DeCS ID: | 34196 | ||||||
Unique ID: | D020967 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2000/01/01 | ||||||
Date of Entry: | 1999/11/03 | ||||||
Revision Date: | 2015/07/06 |
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Myotonic Disorders
- Preferred
Paramyotonia Congenita Without Cold Paralysis
- Narrower
Myotonia Fluctuans
- Narrower
Paramyotonia Congenita
- Narrower
Concept UI |
M0328274 |
Scope note | Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. |
Preferred term | Myotonic Disorders |
Entry term(s) |
Disorder, Myotonic Disorders, Myotonic Myopathies, Myotonic Myopathy, Myotonic Myotonic Disorder Myotonic Myopathies Myotonic Myopathy |
Concept UI |
M0567129 |
Preferred term | Paramyotonia Congenita Without Cold Paralysis |
Concept UI |
M0337319 |
Preferred term | Myotonia Fluctuans |
Concept UI |
M0337321 |
Preferred term | Paramyotonia Congenita |
Entry term(s) |
Eulenburg Disease Eulenburg's Disease Paralysis Periodica Paramyotonia Paramyotonia Congenita of von Eulenberg Von Eulenberg Disease Von Eulenberg's Disease |
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