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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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Hereditary peripheral neuropathy
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Charcot-Marie-Tooth disease
Charcot-marie-tooth disease, axonal, type 2MM
rare
Identifiers
MONDO:0980971
OMIM:621488
Causal genes
COX18
Part of
Charcot-Marie-Tooth disease
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