RGD Annotation Report for Congenital hypothyroidismRat Genome Database

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An association has been curated linking PRKAR1A and Congenital hypothyroidism in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
39 RGD objects have been annotated to Congenital hypothyroidism (HP:0000851)
10 papers in RGD have been used to annotate PRKAR1A
Original References(s): OMIM:101800

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