Disease #02304 (ETL1 (epilepsy, temporal lobe, familial, type 1 (ETL-1)), OMIM:600512)

Official abbreviation ETL1
Name epilepsy, temporal lobe, familial, type 1 (ETL-1)
OMIM ID 600512
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 LGI1
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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00335729 177213 - - M - Germany - - - - - ETL1 Generalised seizures since the age of 13, not febrile, often in the evening, with aura; mother and twin sister also affected. LGI1 LGI1 1 1 Andreas Laner
00375620 179357 - - M no Germany - - - - - ETL1 Generalised seizures since the age of 13y, not febrile, often in the evening, with aura; mother and twin sister also affected. LIG1 - - 1 Andreas Laner
00407682 195223 - - F no Germany - - - - - ETL1 Seizure LGI1 LGI1 1 1 Andreas Laner
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