Search Ontology:
Human Disease
juvenile absence epilepsy 1
- Term ID
- DOID:0111324
- Synonyms
-
- EJA1
- JAE1
- Definition
- A juvenile absence epilepsy that has_material_basis_in heterozygous mutation in EFHC1 on 6p12.2. https://www.ncbi.nlm.nih.gov/pubmed/14663045
- References
- Ontology
- Human Disease ( DOID:0111324 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models