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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
/
Distal myopathy
/
Oculopharyngodistal myopathy
Oculopharyngodistal myopathy 5
rare
Identifiers
MONDO:0980937
OMIM:621446
Causal genes
ABCD3
Part of
Oculopharyngodistal myopathy
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