EEG abnormality, Frontotemporal dementia, Generalized myoclonic seizure, Gliosis, Hallucinations, Hyperorality, Hypersexuality, Lewy bodies, Memory impairment, Mental deterioration, Mutism, Neurofibrillary tangles, Neuronal loss in central nervous system, Optic atrophy, Parkinsonism, Perseveration, Personality changes, Polyphagia, Progressive language deterioration, Repetitive compulsive behavior, Retinal dystrophy, Seizure, Visual impairment

abnormal neurite morphology, abnormal neuron physiology, abnormal paraventricular hypothalamic nucleus morphology, abnormal renal water homeostasis, abnormal response to novel object, abnormal retina ganglion cell morphology, abnormal retina nerve fiber layer morphology, abnormal social investigation, abnormal spatial learning, abnormal supraoptic nucleus morphology, abnormal synapse morphology, abnormal thalamus neuron morphology, behavior/neurological phenotype, decreased a-wave amplitude, decreased aggression towards male mice, decreased b-wave amplitude, decreased brain weight, decreased dendritic spine density, decreased grooming behavior, decreased survivor rate, decreased urine creatinine level, decreased urine osmolality, dilated kidney collecting duct, dilated renal tubules, homeostasis/metabolism phenotype, impaired contextual conditioning behavior, impaired synaptic plasticity, increased aggression towards male mice, increased anxiety-related response, increased circulating antidiuretic hormone level, increased circulating ghrelin level, increased fluid intake, increased food intake, increased grooming behavior, increased hepatocyte karyomegaly, increased interleukin-1 beta secretion, increased interleukin-10 secretion, increased interleukin-12 secretion, increased interleukin-6 secretion, increased kidney weight, increased liver weight, increased susceptibility to dopaminergic neuron neurotoxicity, increased susceptibility to injury, increased thigmotaxis, increased tumor necrosis factor secretion, lipofuscinosis, loss of dopaminergic neurons, microgliosis, nervous system inclusion bodies, nervous system phenotype, neuronal cytoplasmic inclusions, premature death, reduced long term potentiation, retina ganglion cell degeneration, skin lesions, tau protein deposits