neurodegenerative disease +

agenesis of the corpus callosum with peripheral neuropathy
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
childhood-onset neurodegeneration with brain atrophy
familial encephalopathy with neuroserpin inclusion bodies
hereditary ataxia +
Huntington's disease
Huntington's disease-like 2
infantile cerebellar-retinal degeneration
motor neuron disease +
myoclonic cerebellar dyssynergia
neuroacanthocytosis +
neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
neurodegeneration with brain iron accumulation +
neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
neuronal intranuclear inclusion disease
olivopontocerebellar atrophy
plexopathy
primary cerebellar degeneration
secondary Parkinson disease +
SPOAN syndrome
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
synucleinopathy +
tauopathy +

pontocerebellar hypoplasia type 1 +
pontocerebellar hypoplasia type 10
pontocerebellar hypoplasia type 11
pontocerebellar hypoplasia type 12
pontocerebellar hypoplasia type 13
pontocerebellar hypoplasia type 14
pontocerebellar hypoplasia type 15
pontocerebellar hypoplasia type 16
pontocerebellar hypoplasia type 2 +
pontocerebellar hypoplasia type 3
pontocerebellar hypoplasia type 4
pontocerebellar hypoplasia type 5
pontocerebellar hypoplasia type 6
pontocerebellar hypoplasia type 7
pontocerebellar hypoplasia type 8
pontocerebellar hypoplasia type 9