RGD Annotation Report for familial encephalopathy with neuroserpin inclusion bodiesRat Genome Database

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An association has been curated linking CV888364 and familial encephalopathy with neuroserpin inclusion bodies 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
4 RGD objects have been annotated to familial encephalopathy with neuroserpin inclusion bodies (DOID:0050831)
0 papers in RGD have been used to annotate CV888364
Curation Notes: ClinVar Annotator: match by term: Encephalopathy, familial, with neuroserpin inclusion bodies

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