SE-ATLAS

Hemiparkinsonism-hemiatrophy syndrome Pontocerebellar hypoplasia type 2 Manganese poisoning Autosomal dominant spastic paraplegia type 17 Pontocerebellar hypoplasia type 1 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 Cyanide-induced parkinsonism-dystonia Distal hereditary motor neuropathy type 2 Young-onset Parkinson disease ATP13A2-related juvenile neuronal ceroid lipofuscinosis Distal hereditary motor neuropathy type 5 Neuroacanthocytosis Frontotemporal dementia Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Mitochondrial disease Classic pantothenate kinase-associated neurodegeneration Distal hereditary motor neuropathy, Jerash type Amyotrophic lateral sclerosis X-linked distal spinal muscular atrophy type 3 Atypical pantothenate kinase-associated neurodegeneration Multiple sclerosis variant Rare parkinsonian disorder Infantile-onset ascending hereditary spastic paralysis Juvenile primary lateral sclerosis Juvenile amyotrophic lateral sclerosis Postencephalitic parkinsonism Proximal spinal muscular atrophy Distal hereditary motor neuropathy type 7 Caribbean parkinsonism Autosomal dominant striatal neurodegeneration Early-onset parkinsonism-intellectual disability syndrome Perry syndrome Choreoacanthocytosis Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Rapid-onset dystonia-parkinsonism Autosomal dominant proximal spinal muscular atrophy Poliomyelitis X-linked dystonia-parkinsonism Spinal muscular atrophy with respiratory distress type 1 Primary lateral sclerosis Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Young adult-onset distal hereditary motor neuropathy Infantile dystonia-parkinsonism Multiple system atrophy, parkinsonian type Generalized bulbospinal muscular atrophy Huntington disease-like 2 Infantile-onset X-linked spinal muscular atrophy O'Sullivan-McLeod syndrome Postpoliomyelitis syndrome X-linked parkinsonism-spasticity syndrome Proximal spinal muscular atrophy type 1 Dystonia 16 Wilson disease Huntington disease Encephalitis lethargica Monomelic amyotrophy Pantothenate kinase-associated neurodegeneration Mitochondrial DNA depletion syndrome, myopathic form Neurogenic scapuloperoneal syndrome, Kaeser type Behavioral variant of frontotemporal dementia Spinal muscular atrophy associated with central nervous system anomaly McLeod neuroacanthocytosis syndrome Parkinsonian-pyramidal syndrome Hereditary spastic paraplegia Amyotrophie spinale proximale autosomique dominante de l'enfance Dystonie-parkinsonisme de l'adulte Sclérose latérale amyotrophique type 4 Neuropathie motrice distale héréditaire autosomique récessive Amyotrophie spinale proximale autosomique dominante de l'enfance associée à BICD2 Amyotrophie spinale proximale autosomique dominante de l'enfance associée à DYNC1H1 Amyotrophie spinale bénigne congénitale autosomique dominante Maladie du motoneurone Maladie génétique du motoneurone Maladie acquise du motoneurone Syndrome du motoneurone inférieur, forme tardive de l'adulte Syndrome d'agénesie du corps calleux-neuropathie Amyotrophie spinale proximale type 3 Amyotrophie spinale proximale type 2 Démence fronto-temporale, variante d'atrophie temporale à droite Amyotrophie spinale proximale type 4 Maladie de Kennedy Démence sémantique Aphasie primaire progressive non fluente Syndrome parkinsonien rare dû à une maladie neurodégénérative Syndrome parkinsonien rare dû à une intoxication Syndrome post-intervallaire par intoxication au monoxyde de carbone Neuropathie motrice distale héréditaire type 1