dyskinesia, familial, with facial myokymia

Preferred Label : dyskinesia, familial, with facial myokymia;

MeSH note : mutation in ADCY5;

Origin ID

C564676;

UMLS CUI

C1847627;

Currated CISMeF NLP mapping
- Dyskinesia with orofacial involvement, autosomal dominant [OMIM Phenotype]
- Familial dyskinesia and facial myokymia [ORDO Disease]
- Familial dyskinesia and facial myokymia (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- dyskinesias [MeSH Descriptor]
- myokymia [MeSH Descriptor]
Record concept(s)
- dyskinesia, familial, with facial myokymia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyskinesia with orofacial involvement, autosomal dominant [OMIM Phenotype]
- Familial dyskinesia and facial myokymia [ORDO Disease]
- Familial dyskinesia and facial myokymia (disorder) [SNOMED CT concept]