Myoclonic epilepsy of lafora 2

Preferred Label : Myoclonic epilepsy of lafora 2;

Symbol : MELF2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Epilepsy, progressive myoclonic, 2b; Lafora disease 2; EPM2B;

Prefixed ID : #620681;

Détails

Origin ID

620681;

UMLS CUI

C1850764;

Genes related to phenotype
- Nhl repeat-containing protein 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- epilepsy, progressive myoclonic 2B [MeSH concept]
- epilepsy, progressive myoclonic 2B [MeSH Supplementary Concept]

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