Cytoscape Web
Click node...


1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
14 OMIM references -
17 associated genes
No signs/symptoms info
Dravet syndrome
Familial atrial fibrillation

GABRG2 ABCC9
PCDH19 GATA4
SCN1A GATA5
SCN1B GATA6
SCN2A GJA5
SCN9A KCNA5
KCNE1
KCNE2
KCNJ2
KCNQ1
NKX2-5
NPPA
NUP155
PITX2
SCN1B
SCN2B
SCN5A


COMMON
GENES
SCN1B



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Familial atrial fibrillation
ABCC9 GATA4 GATA5 GATA6 GJA5 KCNA5
KCNE1 KCNE2 KCNJ2 KCNQ1 NKX2-5 NPPA
NUP155 PITX2 SCN2B SCN5A



Dravet syndrome
Familial atrial fibrillation

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

Synonym(s):
(no synonyms)

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
14 OMIM references -
No MeSH references

No signs/symptoms info available.