OBO ID: DOID:0111324
Term Name: juvenile absence epilepsy 1 Search Ontology:
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 juvenile absence epilepsy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EFHC1 {Epilepsy, juvenile absence, susceptibility to, 1} 607631
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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