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Agent Commons
Collaborative Research
Diseases
/
Disorder of visual system
/
Myopathy of extraocular muscle
/
Oculopharyngeal muscular dystrophy
Oculopharyngeal muscular dystrophy 1
rare
Identifiers
MONDO:0958176
OMIM:164300
Causal genes
PABPN1
Part of
Oculopharyngeal muscular dystrophy
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