Search Ontology:
Human Disease

juvenile myoclonic epilepsy 3

Term ID
DOID:0111326
Synonyms
  • EJM3
Definition
A juvenile myoclonic epilepsy that has_material_basis_in variation in a region on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/12830434
References
Ontology
Human Disease   ( DOID:0111326 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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