Cytoscape Web
Click node...

Juvenile myoclonic epilepsy
9 OMIM references -
7 associated genes
No signs/symptoms info
COMMON GENES: 1
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile myoclonic epilepsy
Leukoencephalopathy with mild cerebellar ataxia and white matter edema

CACNB4
(UniProt - OMIM)
 CLCN2
(UniProt - OMIM)
CLCN2
(UniProt - OMIM)
EFHC1
(UniProt - OMIM)
GABRA1
(UniProt - OMIM)
GABRD
(UniProt - OMIM)
JRK
(UniProt - OMIM)
KCNQ3
(UniProt - OMIM)

COMMON
GENES 		CLCN2


Citations in the biomedical literature:


Juvenile myoclonic epilepsy
CACNB4 CLCN2 EFHC1 GABRA1 GABRD JRK
KCNQ3
Leukoencephalopathy with mild cerebellar ataxia and white matter edema



Juvenile myoclonic epilepsy
Leukoencephalopathy with mild cerebellar ataxia and white matter edema

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
9 OMIM references -
1 MeSH reference: D020190
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.