SE-ATLAS

ATP13A2-related juvenile neuronal ceroid lipofuscinosis Acquired motor neuron disease Adult-onset dystonia-parkinsonism Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Atypical pantothenate kinase-associated neurodegeneration Autosomal dominant adult-onset proximal spinal muscular atrophy Autosomal dominant childhood-onset proximal spinal muscular atrophy Autosomal dominant congenital benign spinal muscular atrophy Autosomal dominant distal hereditary motor neuropathy Autosomal dominant proximal spinal muscular atrophy Autosomal dominant spastic paraplegia type 17 Autosomal dominant striatal neurodegeneration Autosomal recessive distal hereditary motor neuropathy Autosomal recessive lower motor neuron disease with childhood onset BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Behavioral variant of frontotemporal dementia Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Bulbospinal muscular atrophy of childhood Caribbean parkinsonism Choreoacanthocytosis Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Classic pantothenate kinase-associated neurodegeneration Corpus callosum agenesis-neuronopathy syndrome Cyanide-induced parkinsonism-dystonia DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Delayed encephalopathy due to carbon monoxide poisoning Distal hereditary motor neuropathy type 1 Distal hereditary motor neuropathy type 2 Distal hereditary motor neuropathy type 5 Distal hereditary motor neuropathy type 7 Distal hereditary motor neuropathy, Jerash type Distal spinal muscular atrophy type 3 Dystonia 16 Early-onset parkinsonism-intellectual disability syndrome Encephalitis lethargica Frontotemporal dementia Frontotemporal dementia, right temporal atrophy variant Generalized bulbospinal muscular atrophy Genetic motor neuron disease Hemiparkinsonism-hemiatrophy syndrome Hereditary spastic paraplegia Huntington disease Huntington disease-like 2 Infantile dystonia-parkinsonism Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Kennedy disease Kufor-Rakeb syndrome Lower motor neuron syndrome with late-adult onset Madras motor neuron disease Manganese poisoning McLeod neuroacanthocytosis syndrome Mitochondrial disease Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies Monomelic amyotrophy Motor neuron disease Multiple sclerosis variant Multiple system atrophy, parkinsonian type Neuroacanthocytosis Neurogenic scapuloperoneal syndrome, Kaeser type O'Sullivan-McLeod syndrome Pantothenate kinase-associated neurodegeneration Parkinsonian-pyramidal syndrome Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Perry syndrome Poliomyelitis Pontocerebellar hypoplasia type 1 Pontocerebellar hypoplasia type 2 Postencephalitic parkinsonism Postpoliomyelitis syndrome Primary lateral sclerosis Primary progressive freezing gait Progressive non-fluent aphasia Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Rapid-onset dystonia-parkinsonism Rare parkinsonian disorder Rare parkinsonian syndrome due to intoxication Rare parkinsonian syndrome due to neurodegenerative disease Riboflavin transporter deficiency Semantic dementia Spinal atrophy-ophthalmoplegia-pyramidal syndrome Spinal muscular atrophy associated with central nervous system anomaly Spinal muscular atrophy with respiratory distress type 1 Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Wilson disease X-linked distal spinal muscular atrophy type 3 X-linked dystonia-parkinsonism X-linked parkinsonism-spasticity syndrome Young adult-onset distal hereditary motor neuropathy Young-onset Parkinson disease