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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Hereditary neuromuscular disease
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Distal myopathy
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Oculopharyngodistal myopathy
Oculopharyngodistal myopathy 4
rare
Identifiers
MONDO:0030712
OMIM:619790
Causal genes
RILPL1
Part of
Oculopharyngodistal myopathy
Also known as
OPDM4
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