werner syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_5688)
External Link http://www.omim.org/entry/277700
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1 genes associated with the werner syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
WRN Werner syndrome, RecQ helicase-like