Abnormal pupillary function, Abnormal pyramidal sign, Abnormal saccadic eye movements, Abnormal shoulder morphology, Aggressive behavior, Akinetic mutism, Amyloidosis of peripheral nerves, Anxiety, Apathy, Aphasia, Apnea, Apraxia, Areflexia, Astrocytosis, Ataxia, Attention deficit hyperactivity disorder, Atypical behavior, Babinski sign, Basal ganglia gliosis, Bradykinesia, Central nervous system degeneration, Cerebellar atrophy, Cerebral cortical atrophy, Chorea, Clumsiness, Cognitive impairment, Confusion, Constipation, Deficit in phonologic short-term memory, Delayed speech and language development, Delusion, Dementia, Depression, Diffuse spongiform leukoencephalopathy, Diplopia, Dysarthria, Dysmetria, Dysphagia, EEG abnormality, EEG with persistent abnormal rhythmic activity, Emotional lability, Encephalopathy, Extrapyramidal muscular rigidity, Fever, Focal T2 hyperintense basal ganglia lesion, Frequent falls, Gait ataxia, Gait disturbance, Generalized hypotonia, Gliosis, Global brain atrophy, Hallucinations, Hemiparesis, Hyperactive deep tendon reflexes, Hyperhidrosis, Hyperreflexia, Hypersomnia, Impaired smooth pursuit, Incoordination, Increased CSF protein concentration, Insomnia, Involuntary movements, Irritability, Jaw pain, Jerky head movements, Jerky ocular pursuit movements, Limb ataxia, Loss of facial expression, Lower limb muscle weakness, Mask-like facies, Memory impairment, Muscle weakness, Myoclonus, Neurofibrillary tangles, Neuronal loss in central nervous system, Nystagmus, Parkinsonism, Perseverative thought, Personality changes, Poor fine motor coordination, Poor visual behavior for age, Progressive cerebellar ataxia, Progressive extrapyramidal muscular rigidity, Progressive forgetfulness, Psychosis, Restlessness, Rigidity, Seizure, Senile plaques, Short attention span, Simultanapraxia, Sleep abnormality, Slow saccadic eye movements, Slurred speech, Spastic dysarthria, Spastic hemiparesis, Spasticity, Specific learning disability, Stroke-like episode, Supranuclear gaze palsy, Tremor, Trigeminal neuralgia, Truncal ataxia, Unsteady gait, Urinary retention, Ventriculomegaly, Vestibular nystagmus, Visual impairment, Weight loss

abnormal hippocampus stratum lacunosum morphology, abnormal inhibitory postsynaptic currents, abnormal inhibitory postsynaptic potential, abnormal magnesium ion homeostasis, abnormal muscle fiber morphology, abnormal neuronal precursor proliferation, abnormal neuron differentiation, abnormal neuron proliferation, abnormal object recognition memory, abnormal response to novel object, abnormal sciatic nerve morphology, abnormal skeletal muscle fiber type ratio, abnormal skeletal muscle morphology, abnormal sleep pattern, abnormal spatial working memory, abnormal susceptibility to prion infection, abnormal tail morphology, abnormal tail movements, abnormal T cell differentiation, abnormal voluntary movement, abnormal Wallerian degeneration, amyloid beta deposits, behavior/neurological phenotype, brain vacuoles, circling, decreased brain copper level, decreased CD4-positive, alpha beta T cell number, decreased DN2 thymocyte number, decreased DN4 thymocyte number, decreased double-positive T cell number, decreased grooming behavior, decreased locomotor activity, decreased neuron number, decreased Purkinje cell number, decreased susceptibility to prion infection, decreased thymocyte number, decreased vertical activity, disheveled coat, excessive scratching, hindlimb paralysis, immune system phenotype, impaired acrosome reaction, impaired balance, impaired fertilization, impaired righting response, increased CD8-positive, alpha-beta T cell number, increased DN3 thymocyte number, increased double-negative T cell number, increased gamma-delta T cell number, increased neuron apoptosis, increased pruritus, increased sensitivity to induced morbidity/mortality, increased susceptibility to prion infection, limb grasping, microgliosis, muscle degeneration, muscular atrophy, nervous system phenotype, neuron degeneration, no abnormal phenotype detected, paresis, premature death, premature neuronal precursor differentiation, Purkinje cell degeneration, reduced long term potentiation, skeletal muscle fiber degeneration, spongiform encephalopathy, thin cerebellar molecular layer, thymus atrophy