myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders

Preferred Label : myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders;

Origin ID

C565786;

UMLS CUI

C1858478;

Automatic exact mappings (from CISMeF team)
- Myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [OMIM Phenotype]
MeSH term(s) associated for indexing
- deafness [MeSH Descriptor]
- epilepsies, myoclonic [MeSH Descriptor]
- macular degeneration [MeSH Descriptor]
- mental disorders [MeSH Descriptor]
Record concept(s)
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [OMIM Phenotype]