Cytoscape Web
Click node...


2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
9 OMIM references -
7 associated genes
No signs/symptoms info
Alternating hemiplegia of childhood
Juvenile myoclonic epilepsy

ATP1A2 CACNB4
ATP1A3 CLCN2
CACNA1A EFHC1
SLC1A3 GABRA1
GABRD
JRK
KCNQ3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNA1A
(0.85)
CACNB4



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Juvenile myoclonic epilepsy
CACNB4 CLCN2 EFHC1 GABRA1 GABRD JRK
KCNQ3



Alternating hemiplegia of childhood
Juvenile myoclonic epilepsy

Synonym(s):
- AHC
- Alternating hemiplegia in childhood

Synonym(s):
(no synonyms)

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):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: C536589
External references:
9 OMIM references -
1 MeSH reference: D020190

No signs/symptoms info available.