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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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