All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05408 FAME epilepsy, myoclonic, familial adult (FAME) - - 69 68 CTNND2, MARCH6, RAPGEF2, SAMD12, STARD7, TNRC6A, YEATS2 - autosomal dominant; myoclonic tremor (cortical tremor), infrequent epilepsy with benign clinical course
05407 FAME1;FMCTE1 epilepsy, myoclonic, familial adult, type 1 (FAME1, FMCTE1) 601068 AD 1 1 SAMD12 - autosomal dominant, benign adult familial myoclonic epilepsy (BAFME)
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