Disease #02682 (EIG11;EJM8 (epilepsy, idiopathic, generalized, susceptibility to, type 11 (EIG-11, epilepsy, myoclonic, juvenile, type 8(EJM-8))), OMIM:607628)

Official abbreviation EIG11;EJM8
Name epilepsy, idiopathic, generalized, susceptibility to, type 11 (EIG-11, epilepsy, myoclonic, juvenile, type 8(EJM-8))
OMIM ID 607628
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CLCN2
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.