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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
5 OMIM references -
4 associated genes
1 sign/symptom
Dravet syndrome
Familial progressive cardiac conduction defect

GABRG2 NKX2-5
PCDH19 SCN1B
SCN1A SCN5A
SCN1B TRPM4
SCN2A
SCN9A


COMMON
GENES
SCN1B



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Familial progressive cardiac conduction defect
NKX2-5 SCN5A TRPM4



Dravet syndrome
Familial progressive cardiac conduction defect

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

Synonym(s):
- Familial Lenègre disease
- Familial Lev disease
- Familial Lev-Lenègre disease
- Familial PCCD
- Familial progressive heart block
- Hereditary bundle branch defect

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 / 1 000 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant

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

Familial progressive cardiac conduction defect

Frequent
- Cardiac rhythm disorder / arrhythmia



Dravet syndrome

(no data available)