Search Ontology:
Human Disease

juvenile myoclonic epilepsy 10

Term ID
DOID:0111325
Synonyms
  • EJM10
Definition
A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1. https://www.ncbi.nlm.nih.gov/pubmed/29539279
References
Ontology
Human Disease   ( DOID:0111325 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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