OBO ID: DOID:0111315 |
Term Name: | idiopathic generalized epilepsy 14 | Search Ontology: | |
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Definition: | An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC12A5 on chromosome 20q13.12. https://www.ncbi.nlm.nih.gov/pubmed/24928908 | ||
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Ontology: | Human Disease ( DOID:0111315 ) |
OTHER idiopathic generalized epilepsy 14 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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