All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05587 FAME-3;FMCTE-3 epilepsy, myoclonic, familial adult, type 3 (FAME-3, FMCTE-3) 613608 0 0 MARCH6 - autosomal dominant
05408 FAME;FMCTE epilepsy, myoclonic, familial adult (FAME familial cortical myoclonic tremor associated with epilepsy (FMCTE)) - 5 5 CTNND2, MARCH6, RAPGEF2, SAMD12, STARD7, TNRC6A - autosomal dominant; myoclonic tremor (cortical tremor), infrequent epilepsy with benign clinical course