Wolcott-Rallison syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure. (Orphanet Rare Disease Ontology, Orphanet_1667)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536739
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1 genes/proteins associated with the disease Wolcott-Rallison syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3 2.88009