RS587778771 PRRT2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Episodic kinesigenic dyskinesia 1
Episodic kinesigenic dyskinesia
Seizures
benign familial infantile
2
Inborn genetic diseases
Infantile convulsions and choreoathetosis
PRRT2-related disorder
PRRT2-associated paroxysmal movement disorder
Benign familial neonatal-infantile seizures 1
Episodic kinesigenic dyskinesia 1
Infantile convulsions and choreoathetosis
Seizure
Seizures
benign familial infantile
Other Variants in PRRT2