OBO ID: DOID:0111312
Term Name: idiopathic generalized epilepsy 11 Search Ontology:
Synonyms:
  • EIG11
Definition: An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1. https://www.ncbi.nlm.nih.gov/pubmed/19710712
References:
Ontology: Human Disease   (DOID:0111312)
Relationships
is a type of:
OTHER idiopathic generalized epilepsy 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLCN2 {Epilepsy, juvenile absence, susceptibility to, 2} 607628
{Epilepsy, juvenile myoclonic, susceptibility to, 8} 607628
{Epilepsy, idiopathic generalized, susceptibility to, 11} 607628
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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