Seizures, benign familial infantile, 5

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Subtype of: Seizures
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Seizures, benign familial infantile, 5
MONDO_0014903
SCN8A Causal
26677014 22365152 16236810 31625145 24194747 27210545 27864847 28923014
Open Targets
All1 Causal1 Unknown0
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Cognitive impairment with or without cerebellar ataxia 1 shared geneSCN8A Related via 1 shared gene including SCN8A. Paroxysmal kinesigenic dyskinesias 1 shared geneSCN8A Related via 1 shared gene including SCN8A. Myoclonus, familial, 2 1 shared geneSCN8A Related via 1 shared gene including SCN8A. Benign infantile epilepsy 1 shared geneSCN8A Related via 1 shared gene including SCN8A. Choreoathetosis 1 shared geneSCN8A Related via 1 shared gene including SCN8A.