deafness, congenital, and familial myoclonic epilepsy

Preferred Label : deafness, congenital, and familial myoclonic epilepsy;

Origin ID

C565649;

UMLS CUI

C1857348;

Currated CISMeF NLP mapping
- Deafness, congenital, and familial myoclonic epilepsy [OMIM Phenotype]
MeSH term(s) associated for indexing
- deafness [MeSH Descriptor]
- epilepsies, myoclonic [MeSH Descriptor]
Record concept(s)
- deafness, congenital, and familial myoclonic epilepsy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, congenital, and familial myoclonic epilepsy [OMIM Phenotype]