RGD Annotation Report for Fraser syndrome 3Rat Genome Database

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An association has been curated linking MYO18B and Fraser syndrome 3 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
The annotation has been inferred by association of genotype and phenotype with RGD:38597954 (Homo sapiens)
17 RGD objects have been annotated to Fraser syndrome 3 (DOID:0111406)
3 papers in RGD have been used to annotate MYO18B
Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 3
Original References(s): PMID:28492532

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