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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Hereditary neuromuscular disease
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Distal myopathy
/
Oculopharyngodistal myopathy
Oculopharyngodistal myopathy 3
rare
Identifiers
MONDO:0023671
OMIM:619473
Causal genes
NOTCH2NLC
Part of
Oculopharyngodistal myopathy
Also known as
OPDM3
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