Muscular Dystrophy, Oculopharyngeal 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_11719)
External Link
Similar Terms
Downloads & Tools


1 genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PABPN1 poly(A) binding protein, nuclear 1 2.88009