Cytoscape Web
Click node...

Juvenile absence epilepsy
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Juvenile myoclonic epilepsy
Synonym(s):
- JAE
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C535495
Gene symbol UniProt reference OMIM reference
EFHC1 Q5JVL4608815
No signs/symptoms info available.