SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:121200
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Genes

1 genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2 2.88009