Disease #05407 (FAME1;FMCTE1 (epilepsy, myoclonic, familial adult, type 1 (FAME1, FMCTE1)), OMIM:601068)

Official abbreviation FAME1;FMCTE1
Name epilepsy, myoclonic, familial adult, type 1 (FAME1, FMCTE1)
OMIM ID 601068
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SAMD12
Associated tissues -
Disease features autosomal dominant, benign adult familial myoclonic epilepsy (BAFME)
Remarks -
Date created 2018-03-18 15:37:28 +01:00 (CET)
Date last edited 2019-12-19 19:05:33 +01:00 (CET)


Individuals

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00275484 - - - - - - - - - - - FAME1;FMCTE1 - SAMD12 SAMD12 1 1 Melanie Bahlo
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