FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term juvenile myoclonic epilepsy 10 ID (Ontology) DOID:0111325 (Human Disease)
Definition A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1.
Also Known As "EJM10"
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 Genes
 juvenile myoclonic epilepsy 10       1
 for disease ribbon | juvenile myoclonic epilepsy 10       1
 model of | juvenile myoclonic epilepsy 10       1
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  adolescence-adult electroclinical syndrome
   |__juvenile myoclonic epilepsy
       |__juvenile myoclonic epilepsy 10  1 rec.
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Is a juvenile myoclonic epilepsy
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Synonyms
  • "EJM10" EXACT OMO:0003012
Secondary IDs
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MIM:617924