Search Ontology:
Human Disease

idiopathic generalized epilepsy 12

Term ID
DOID:0111313
Synonyms
  • EIG12
Definition
An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2. https://www.ncbi.nlm.nih.gov/pubmed/19798636
References
Ontology
Human Disease   ( DOID:0111313 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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