familial cortical myoclonic tremor with epilepsy 2

Preferred Label : familial cortical myoclonic tremor with epilepsy 2;

Obsolete resource : true;

Approved symbol HGNC : FCMTE2;

Name synonyms HGNC : cortical myoclonus and epilepsy; autosomal dominant; benign adult familial myoclonic epilepsy 2; familial adult myoclonic epilepsy 2;

Alias symbols HGNC : FAME2; BAFME2; ADCME;

Chromosome HGNC : 2p11.1-q12.2;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:37159;

UMLS CUI

C2829392;

See also inter- (CISMeF)
- Epilepsy, familial adult myoclonic, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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