| disease_description | Multiple system atrophy, cerebellar variant,Frontotemporal dementia,Multiple System Atrophy,Myotonic Dystrophy,Corticobasal degeneration,AMYOTROPHIC LATERAL SCLEROSIS 1,Restless Legs Syndrome,Huntington Disease,Lateral Sclerosis,Amyotrophic Lateral Sclerosis With Dementia,Juvenile arthritis,Progressive Muscular Atrophy,Nonorganic psychosis,Movement Disorders,Spinal Muscular Atrophy,Psychotic Disorders,Semantic Dementia,Extrapyramidal sign,Parkinsonian Disorders,FRAGILE X TREMOR/ATAXIA SYNDROME,Motor Neuron Disease,Schizoaffective Disorder,Plaque, Amyloid,Hamartoma,Shy-Drager Syndrome,Spastic Paraplegia,Pain,Congenital Myotonic Dystrophy,Mild cognitive disorder,Amyotrophic Lateral Sclerosis,Impaired cognition,nervous system disorder,Amyotrophic Lateral Sclerosis, Sporadic,Ganglioneuroma,Aphasia, Progressive,Psychiatric symptom,Pick Disease of the Brain,Huntington Disease-Like Syndrome,AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1,GRN-related frontotemporal dementia,Hall |