Prader-Willi Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11983)
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3 genes/proteins associated with the disease Prader-Willi Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MAGEL2 melanoma antigen family L2 2.88009
SNRPN small nuclear ribonucleoprotein polypeptide N 2.88009
NDN necdin, melanoma antigen (MAGE) family member 2.88009