SE-ATLAS

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