Disease #02502 (FFEVF1 (epilepsy, familial focal, with variable foci, type 1), OMIM:604364)

Official abbreviation FFEVF1
Name epilepsy, familial focal, with variable foci, type 1
OMIM ID 604364
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene DEPDC5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00395430 189478 - - F no Germany - - - - - FFEVF1 Frontal lobe epilepsy since the age of 16 months, right fronto-basal gyration disorder DEPDC5 DEPDC5 1 1 Andreas Laner
00398737 190426 - - F - Turkey - - - - - FFEVF1 Generalized-onset seizure, Mild global developmental delay, Interictal EEG abnormality; brother also affected (untested) DEPDC5 DEPDC5 1 1 Andreas Laner
00466579 344396 - - M no (China) - - - - - FFEVF1 Nocturnal seizures, Bilateral tonic-clonic seizure with generalized onset DEPDC5 DEPDC5 1 1 Andreas Laner
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