oculopharyngeal muscular dystrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11719)
External Link http://www.omim.org/entry/164300
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1 genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

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