Severe myoclonic epilepsy in infancy Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An epilepsy that is characterized by frequent febrile seizures with onset before 1 year. (Human Disease Ontology, DOID_0060171)
External Link http://www.omim.org/entry/607208
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Genes

1 genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SCN1A sodium channel, voltage gated, type I alpha subunit