muscular dystrophy, oculopharyngeal Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11719)
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1 genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
PABPN1 poly(A) binding protein, nuclear 1