RS200965749 SCN9A
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Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Self-limited epilepsy with centrotemporal spikes
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Self-limited epilepsy with centrotemporal spikes
Inborn genetic diseases
Other Variants in SCN9A