Cytoscape Web
Click node...

Female restricted epilepsy with intellectual deficit
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Dravet syndrome
Synonym(s):
- EFMR
- Familial epilepsy and mental retardation limited to females
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: unknown
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
PCDH19 Q8TAB3300460
No signs/symptoms info available.