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- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Myotonic Disorders
- Standard Disease Name
- myotonic disorders
- MeSH Tree
- No data
- ICD-10
- G71.1
Identifiers
- DO ID
- No data
- MeSH ID
- D020967
- OMIM ID
- No data
- UMLS ID
- C0553604
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An inherited or acquired, localized or generalized disorder affecting the muscles. It may be associated with abnormalities in the chloride or sodium channels of the muscles. It is characterized by delayed muscle relaxation following stimulation or contraction. Representative examples include myotonia congenita and myotonic dystrophy.|MSH2017_2016_08_12: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.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease8 Targets
02
03
CNBP
CCHC-type zinc finger nucleic acid binding protein
CCHC-type zinc finger nucleic acid binding protein
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