Myokymia - CISMeF

Preferred Label : Myokymia;

NCIt definition : A disorder characterized by involuntary and irregular muscle contractions not associated with muscle weakness or atrophy. It most often affects facial muscles. It may be localized or generalized.;

Details

Origin ID

C84911;

UMLS CUI

C0684219;

Automatic exact mappings (from CISMeF team)
- Myokymia [ICD-11 Sub-sub category]
Currated CISMeF NLP mapping
- Myokymia [PASCAL descriptor]
- Myokymia [HPO term]
- Myokymia [MedDRA Preferred Term]
- Myokymia (finding) [SNOMED CT concept]
- myokymia [Disease (Nov.)]
- myokymia [MeSH Descriptor]
- myokymia [MeSH concept]
- myokymia [SNOMED Notion]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Semantic type(s)
- Sign or Symptom [UMLS semantic type]
UMLS correspondences (same concept)
- Morvan syndrome [SNOMED Notion]
- Morvan syndrome [ORDO Disease]
- Morvan's fibrillary chorea [MedDRA LLT]
- Myokymia [HPO term]
- Myokymia [PASCAL descriptor]
- Myokymia [MedDRA Preferred Term]
- Myokymia (finding) [SNOMED CT concept]
- myokymia [Disease (Nov.)]
- myokymia [MeSH concept]
- myokymia [MeSH Descriptor]
- myokymia [SNOMED Notion]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
related_to_genetic_biomarker
- KCNQ2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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