SE-ATLAS

Acute motor axonal neuropathy Acute motor and sensory axonal neuropathy Miller Fisher syndrome Adult-onset myasthenia gravis Nasu-Hakola disease X-linked adrenoleukodystrophy Congenital or early infantile CACH syndrome Myasthenia gravis Neonatal adrenoleukodystrophy CADDS Late infantile CACH syndrome Hypomyelination with atrophy of basal ganglia and cerebellum Leukoencephalopathy with bilateral anterior temporal lobe cysts Aicardi-Goutières syndrome Juvenile myasthenia gravis Leukoencephalopathy with mild cerebellar ataxia and white matter edema Juvenile or adult CACH syndrome Metachromatic leukodystrophy, late infantile form Hypomyelination-congenital cataract syndrome Guillain-Barré syndrome Progressive cavitating leukoencephalopathy Pelizaeus-Merzbacher disease, connatal form Alexander disease Allan-Herndon-Dudley syndrome Metachromatic leukodystrophy, juvenile form Hypomyelination with brain stem and spinal cord involvement and leg spasticity Transient neonatal myasthenia gravis 4H leukodystrophy Pelizaeus-Merzbacher disease, classic form Metachromatic leukodystrophy, adult form Pelizaeus-Merzbacher disease in female carriers Krabbe disease Unknown leukodystrophy Infantile Krabbe disease Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Late-infantile/juvenile Krabbe disease 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