SE-ATLAS

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