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1 OMIM reference -
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
11 OMIM references -
13 associated genes
No signs/symptoms info
Dravet syndrome
Romano-Ward syndrome

GABRG2 AKAP9
PCDH19 ALG10
SCN1A ANK2
SCN1B CAV3
SCN2A KCNE1
SCN9A KCNE2
KCNH2
KCNJ5
KCNQ1
NOS1AP
SCN4B
SCN5A
SNTA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SCN1A
SCN2A
(0.76)
(0.55)
SNTA1
SCN4B



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Romano-Ward syndrome
AKAP9 ALG10 ANK2 CAV3 KCNE1 KCNE2
KCNH2 KCNJ5 KCNQ1 NOS1AP SCN4B SCN5A
SNTA1



Dravet syndrome
Romano-Ward syndrome

Synonym(s):
- SMEI
- Severe myoclonic epilepsy of infancy

Synonym(s):
- Romano-Ward long QT syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the circulatory 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: 1-5 / 10 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
11 OMIM references -
1 MeSH reference: D029597

No signs/symptoms info available.