Search Ontology:
Human Disease

obsolete idiopathic generalized epilepsy 11

Term ID
DOID:0111312
Synonyms
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
Obsolete
true
Ontology
Human Disease   ( DOID:0111312 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.