RGD Annotation Report for Larsen syndromeRat Genome Database

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An association has been curated linking CV889492 and Larsen 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
5 RGD objects have been annotated to Larsen syndrome (DOID:14764)
0 papers in RGD have been used to annotate CV889492
Curation Notes: ClinVar Annotator: match by term: FLNB-Related Spectrum Disorders

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