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Dravet syndrome
1 OMIM reference -
6 associated genes
30 connected diseases
No signs/symptoms info
Disease Type of connection
Generalized epilepsy with febrile seizures-plus context
Benign familial infantile seizures
Benign familial neonatal-infantile seizures
Brugada syndrome
Channelopathy-associated congenital insensitivity to pain
Childhood absence epilepsy
Early infantile epileptic encephalopathy
Epilepsy with myoclonic-astatic seizures
Familial atrial fibrillation
Familial or sporadic hemiplegic migraine
Familial progressive cardiac conduction defect
Female restricted epilepsy with intellectual deficit
Hereditary sensory and autonomic neuropathy type 2
Lennox-Gastaut syndrome
Malignant migrating partial seizures of infancy
Paroxysmal extreme pain disorder
Primary erythermalgia
Sodium channelopathy-related small fiber neuropathy
West syndrome
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Romano-Ward syndrome
Autosomal dominant cervical dystonia
Benign essential blepharospasm
Congenital lethal myopathy, Compton-North type
Behavioral variant of frontotemporal dementia
Early-onset autosomal dominant Alzheimer disease
Familial isolated dilated cardiomyopathy
Progressive non-fluent aphasia
Semantic dementia
- Severe myoclonic epilepsy of infancy

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

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
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.