RGD Annotation Report for congenital hypothyroidismRat Genome Database

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An association has been curated linking Runx2 and congenital hypothyroidism in Rattus norvegicus.

The association was inferred from sequence or structural similarity (ISS)
The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
The annotation has been inferred from sequence or structural similarity with Runx2 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
234 RGD objects have been annotated to congenital hypothyroidism (DOID:0050328)
31 papers in RGD have been used to annotate Runx2

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