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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
Peripheral motor neuropathy, childhood-onset, biotin-responsive
rare
Identifiers
MONDO:0859255
OMIM:619903
Causal genes
SLC5A6
Part of
Hereditary peripheral neuropathy
Motor peripheral neuropathy
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