SE-ATLAS

Foix-Chavany-Marie syndrome Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Corticobasal syndrome Progressive supranuclear palsy-corticobasal syndrome Dubowitz syndrome Leigh syndrome Distal hereditary motor neuropathy type 2 Infantile-onset ascending hereditary spastic paralysis Cockayne syndrome Classic progressive supranuclear palsy syndrome Distal hereditary motor neuropathy type 1 Progressive muscular atrophy Multiple system atrophy, cerebellar type Distal hereditary motor neuropathy type 5 Progressive supranuclear palsy-parkinsonism syndrome Neuronal intranuclear inclusion disease Infantile neuroaxonal dystrophy Distal hereditary motor neuropathy, Jerash type Distal hereditary motor neuropathy type 7 Huntington disease Motor neuron disease Frontotemporal degeneration with dementia MELAS Susac syndrome Amyotrophic lateral sclerosis type 4 Kennedy disease Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Noonan syndrome Aarskog-Scott syndrome Subacute sclerosing leukoencephalitis Moyamoya disease Seckel syndrome Progressive supranuclear palsy Amyotrophic lateral sclerosis Robinow syndrome Multiple system atrophy, parkinsonian type Madras motor neuron disease Logopenic progressive aphasia ITM2B amyloidosis Smith-Lemli-Opitz syndrome Frontotemporal dementia, right temporal atrophy variant Primary lateral sclerosis Neuropathie, distale kongenitale motorische, des jungen Erwachsenen Spinale Atrophie-Ophthalmoplegie-Pyramidenbahn-Symptomatik-Syndrom Moyamoya-Krankheit mit früh-einsetzender Achalasie Neuropathie, distale hereditäre motorische, X-chromosomale HERNS-Syndrom Watson-Syndrom Primäre Angiitis des Zentralnervensystems Aphasie, primäre progressive Semantische Demenz Vorderhornerkrankung, autosomal-rezessive, des Kindes Neuromyelitis-optica-Spektrum-Störung Mikrodeletionssyndrom 17q11 Neuropathy, motorische, distale, hereditäre, autosomal-rezessive Monosomie 22q13 Progressive supranukleäre Blickparese, atypische Lateralsklerose, juvenile primäre Amyotrophe Lateralsklerose, juvenile Striatale Nekrose, bilaterale infantile, sporadische Form Verhaltensvariante der frontotemporalen Demenz Aphasie, nicht-flüssige progrediente Guam-Parkinson-Demenz-Komplex Enzephalitis, infektiöse Reversibles zerebrales Vasokonstriktionssyndrom Familiäres zerebrales sakkuläres Aneurysma Zerebrale Sinus- und Venenthrombose Striatale Nekrose, infantile Striatale Nekrose, infantile familiäre Frontotemporale Demenz Legius-Syndrom Hereditäre spastische Paraplegie Atrophie, kortikale posteriore Enzephalitis Neurofibromatose Typ 1 Schwannomatose, NF2-assoziierte