facial palsy, familial recurrent peripheral

Preferred Label : facial palsy, familial recurrent peripheral;

Origin ID

C565028;

UMLS CUI

C1851399;

Automatic exact mappings (from CISMeF team)
- Familial recurrent peripheral facial palsy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Facial palsy, familial recurrent peripheral [OMIM Phenotype]
- Familial recurrent peripheral facial palsy [ORDO Disease]
MeSH term(s) associated for indexing
- facial paralysis [MeSH Descriptor]
Record concept(s)
- facial palsy, familial recurrent peripheral [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Facial palsy, familial recurrent peripheral [OMIM Phenotype]
- Familial recurrent peripheral facial palsy [ORDO Disease]
- Familial recurrent peripheral facial palsy (disorder) [SNOMED CT concept]