RGD Annotation Report for benign neonatal seizuresRat Genome Database

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An association has been curated linking CV312915 and benign neonatal seizures in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
20 RGD objects have been annotated to benign neonatal seizures (DOID:14264)
0 papers in RGD have been used to annotate CV312915
Curation Notes: ClinVar Annotator: match by term: Benign Neonatal Epilepsy

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.