Search Ontology:
Human Disease

juvenile myoclonic epilepsy 9

Term ID
DOID:0111328
Synonyms
  • EJM9
Definition
A juvenile myoclonic epilepsy that has_material_basis_in heterozygous variation in a region on chromosome 2q33-q36. https://www.ncbi.nlm.nih.gov/pubmed/20467754
References
Ontology
Human Disease   ( DOID:0111328 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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