Any neurodegenerative disorder in which the cause of the disease is a mutation in the DCTN1 gene.
Comprehensive, easy-to-understand information about this condition
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Huntington disease and related disorders
MONDO:0000167
agenesis of the corpus callosum with peripheral neuropathy
MONDO:0000902
striatonigral degeneration
MONDO:0003122
angioid streaks of choroid
MONDO:0004882
amyotrophic lateral sclerosis-parkinsonism-dementia complex
MONDO:0007104
inherited Creutzfeldt-Jakob disease
MONDO:0007403