RGD Annotation Report for Cerebellar atrophyRat Genome Database

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An association has been curated linking CKAP2L and Cerebellar atrophy 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
463 RGD objects have been annotated to Cerebellar atrophy (HP:0001272)
3 papers in RGD have been used to annotate CKAP2L
Original References(s): MIM:272440

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