SE-ATLAS

Neuropathie, akute axonale motorische Neuropathie, akute axonale motorisch-sensorische Miller-Fisher-Syndrom Myasthenia gravis mit Beginn im Erwachsenenalter Nasu-Hakola-Krankheit Adrenoleukodystrophie, X-chromosomale CACH-Syndrom, kongenitales oder früh-infantile Form Myasthenia gravis Adrenoleukodystrophie, neonatale Form CADDS CACH-Syndrom, spät-infantile Form Hypomyelinisierung mit Atrophie der Basalganglien und des Kleinhirns Leukoenzephalopathie mit beiderseitigen vorderen Temporallappen-Zysten Aicardi-Goutières-Syndrom Juvenile Myasthenia gravis Leukoenzephalopathie mit milder zerebellärer Ataxie und Ödem der weißen Substanz CACH-Syndrom, juvenile oder adulte Form Leukodystrophie, metachromatische, spät-infantile Form Hypomyelinisierung - kongenitale Katarakt Guillain-Barré-Syndrom Leukoenzephalopathie, kavitierende progressive Pelizaeus-Merzbacher-Krankheit, konnatale Form Alexander-Krankheit Allan-Herndon-Dudley-Syndrom Leukodystrophie, metachromatische, juvenile Form Hypomyelinisierung mit Hirnstamm- und Rückenmarkbeteiligung und Beinspastik Transiente neonatale Myasthenia gravis 4H-Leukodystrophie Pelizaeus-Merzbacher-Krankheit, klassische Form Leukodystrophie, metachromatische, adulte Form Pelizaeus-Merzbacher-Krankheit, weibliche Überträgerinnen Krabbe-Syndrom Leukodystrophie unbekannter Ursache Krabbe-Syndrom, infantile Form Periphere demyelinisierende Neuropathie-zentrale demyelinisierende Leukodystrophie-Waardenburg-Syndrom-Hirschsprung Krankheit Krabbe-Syndrom, spät-infantiles oder juveniles Pelizaeus-Merzbacher disease, transitional form Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Peroxisome biogenesis disorder Infantile Refsum disease Cerebrotendinous xanthomatosis Null syndrome Adult Krabbe disease Refsum disease Alexander disease type I Zellweger syndrome Variant of Guillain-Barré syndrome Odontoleukodystrophy Functional variant of Guillain-Barré syndrome Regional variant of Guillain-Barré syndrome Metachromatic leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome Alexander disease type II Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Pelizaeus-Merzbacher-like disease Paraparetic variant of Guillain-Barré syndrome Severe Canavan disease Pelizaeus-Merzbacher-like disease due to GJC2 mutation Mild Canavan disease Spastic paraplegia type 2 Acute pure sensory neuropathy CACH syndrome Acute pandysautonomia Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Canavan disease X-linked cerebral adrenoleukodystrophy Acute sensory ataxic neuropathy Adult-onset autosomal dominant leukodystrophy Adrenomyeloneuropathy Leukoencephalopathy-dystonia-motor neuropathy syndrome Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Ovarioleukodystrophy Ravine syndrome Cree leukoencephalopathy Pelizaeus-Merzbacher disease Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Leukodystrophy Megalencephalic leukoencephalopathy with subcortical cysts Cystic leukoencephalopathy without megalencephaly Acute inflammatory demyelinating polyradiculoneuropathy Bickerstaff brainstem encephalitis