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

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 604363;

Details

Origin ID

604363;

UMLS CUI

C1858478;

Automatic exact mappings (from CISMeF team)
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH concept]
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH Supplementary Concept]
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH concept]

Keyword's position in hierarchy(ies) :

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