Parent term(s)
Term with siblings
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
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 +
SPOAN syndrome
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
synucleinopathy +
tauopathy +
neuroacanthocytosis +
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
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 +
SPOAN syndrome
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
synucleinopathy +
tauopathy +
Child term(s)
denotes an 'is-a' relationship