Seizures, benign familial infantile, 2

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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, 2
MONDO_0017615
PRRT2 Causal
23126439 22101681 31193310 22399141 22120146 36247910 38316952 25595153 22744660 22243967 22623405
Open Targets —
All1 Causal1 Unknown0
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Familial infantile convulsions with paroxysmal choreoathetosis 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Paroxysmal dystonia 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Infantile convulsions and choreoathetosis 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Neurodevelopmental and movement disorder with or without seizures 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Movement disorders 1 shared genePRRT2 Related via 1 shared gene including PRRT2.