RGD Annotation Report for Abnormality of movementRat Genome Database

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An association has been curated linking PDE8B and Abnormality of movement 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
2936 RGD objects have been annotated to Abnormality of movement (HP:0100022)
7 papers in RGD have been used to annotate PDE8B
Original References(s): ORPHA:228169

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