Disease #03200 (EIG8 (epilepsy, idiopathic, generalized, susceptibility to, type 8 (EIG-8)), OMIM:612899)

Official abbreviation EIG8
Name epilepsy, idiopathic, generalized, susceptibility to, type 8 (EIG-8)
OMIM ID 612899
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene CASR
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

6 entries on 1 page. Showing entries 1 - 6.
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00204947 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
00205024 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
00205103 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
00205109 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
00205110 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
00205111 - - - - ? - - - - - - EIG8 - CASR CASR 1 1 LOVD
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