OBO ID: DOID:0111313
Term Name: idiopathic generalized epilepsy 12 Search Ontology:
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 idiopathic generalized epilepsy 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC2A1 {Epilepsy, idiopathic generalized, susceptibility to, 12} 614847
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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