facial palsy, congenital, unilateral or bilateral

Preferred Label : facial palsy, congenital, unilateral or bilateral;

Origin ID

C563309;

UMLS CUI

C4551949;

Currated CISMeF NLP mapping
- Facial paresis, hereditary congenital, 1 [OMIM Phenotype]
- Isolated hereditary congenital facial paralysis [ORDO Disease]
MeSH term(s) associated for indexing
- facial asymmetry [MeSH Descriptor]
- facial nerve diseases [MeSH Descriptor]
- facial paralysis [MeSH Descriptor]
Record concept(s)
- facial palsy, congenital, unilateral or bilateral [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]