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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, demyelinating, type 1J
rare
Identifiers
MONDO:0859311
OMIM:620111
Causal genes
ITPR3
Part of
Charcot-Marie-Tooth disease
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