Parent term(s)
neurodegenerative disease
+
Term with siblings
Huntington's 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
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Huntington's disease-like 2
infantile cerebellar-retinal degeneration
motor neuron disease
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myoclonic cerebellar dyssynergia
neuroacanthocytosis
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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
pontocerebellar hypoplasia
+
primary cerebellar degeneration
secondary Parkinson disease
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SPOAN syndrome
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
synucleinopathy
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tauopathy
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Child term(s)
denotes an 'is-a' relationship