RGD Annotation Report for autosomal dominant nocturnal frontal lobe epilepsyRat Genome Database

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An association has been curated linking CV558124 and autosomal dominant nocturnal frontal lobe epilepsy 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
123 RGD objects have been annotated to autosomal dominant nocturnal frontal lobe epilepsy (DOID:0060681)
0 papers in RGD have been used to annotate CV558124
Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nocturnal frontal lobe epilepsy
Original References(s): PMID:28492532

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