SE-ATLAS

Syndrome scapulo-péronier neurogénique type Kaeser Amyotrophie spinale proximale autosomique dominante Amyotrophie spinale avec détresse respiratoire type 1 Syndrome parkinsonien et spasticité liés à l'X Dystonie-parkinsonisme infantile Poliomyélite Neurodégénérescence par déficit en pantothénate kinase Dystonie-parkinsonisme à début rapide Maladie mitochondriale Maladie de Huntington-like 2 Atrophie multisystématisée type parkinsonien Amyotrophie spinale infantile liée à l'X Sclérose latérale primitive juvénile Neuropathie motrice distale héréditaire type 7 Paralysie spastique infantile ascendante héréditaire Syndrome de parkinsonisme précoce-déficience intellectuelle Syndrome parkinsonien rare dû à une maladie neurodégénérative Démence fronto-temporale, variante d'atrophie temporale à droite Syndrome d'hémiparkinsonisme-hémiatrophie Syndrome parkinsonien rare dû à une intoxication Syndrome parkinsonien rare Amyotrophie bulbospinale Hypoplasie pontocérébelleuse type 2 Chorée-acanthocytose Intoxication au manganèse Paraplégie spastique autosomique dominante type 17 Amyotrophie spinale proximale Amyotrophie bulbospinale de l'adulte Syndrome de Kufor-Rakeb Hypoplasie pontocérébelleuse type 1 Maladie de Kennedy Neuroacanthocytose Amyotrophie bulbospinale de l'enfant Amyotrophie spinale généralisée Démence fronto-temporale, variante comportementale Syndrome post-poliomyélite Amyotrophie monomélique Amyotrophie spinale proximale type 2 Syndrome post-intervallaire par intoxication au monoxyde de carbone Amyotrophie spinale proximale type 4 Amyotrophie spinale proximale 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