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KIF5A-related neurological disorder
MONDO:0100629Any nervous system disorder in which the cause of the disease is a variation in the KIF5A gene.
Also known as: KIF5A-RD, KIF5A-related disorder, kinesin family member 5A (KIF5A)-related disorder
0 clinical trials for this condition and its sub-types, 0 tagged with KIF5A-related neurological disorder itself.
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Browse by category →Sub-types of KIF5A-related neurological disorder
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Hereditary spastic paraplegia 10 0 trials
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Myoclonus, intractable, neonatal 0 trials
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