RGD Annotation Report for Frank-Ter Haar syndromeRat Genome Database

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An association has been curated linking CV893881 and Frank-Ter Haar syndrome 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
1 RGD objects have been annotated to Frank-Ter Haar syndrome (DOID:0111789)
0 papers in RGD have been used to annotate CV893881
Curation Notes: ClinVar Annotator: match by term: Frank-Ter Haar syndrome

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