SE-ATLAS

4H leukodystrophy Acute inflammatory demyelinating polyradiculoneuropathy Acute motor and sensory axonal neuropathy Acute motor axonal neuropathy Acute pandysautonomia Acute pure sensory neuropathy Acute sensory ataxic neuropathy Adrenomyeloneuropathy Adult Krabbe disease Adult-onset autosomal dominant leukodystrophy Adult-onset myasthenia gravis Aicardi-Goutières syndrome Alexander disease Alexander disease type I Alexander disease type II Allan-Herndon-Dudley syndrome Bickerstaff brainstem encephalitis CACH syndrome CADDS Canavan disease Cerebrotendinous xanthomatosis Congenital or early infantile CACH syndrome Cree leukoencephalopathy Cystic leukoencephalopathy without megalencephaly Functional variant of Guillain-Barré syndrome Guillain-Barré syndrome Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Hypomyelination with atrophy of basal ganglia and cerebellum Hypomyelination with brain stem and spinal cord involvement and leg spasticity Hypomyelination-congenital cataract syndrome Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Infantile Krabbe disease Infantile Refsum disease Juvenile myasthenia gravis Juvenile or adult CACH syndrome Krabbe disease Late infantile CACH syndrome Late-infantile/juvenile Krabbe disease Leukodystrophy Leukoencephalopathy with bilateral anterior temporal lobe cysts Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Leukoencephalopathy with mild cerebellar ataxia and white matter edema Leukoencephalopathy-dystonia-motor neuropathy syndrome Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Megalencephalic leukoencephalopathy with subcortical cysts Metachromatic leukodystrophy Metachromatic leukodystrophy, adult form Metachromatic leukodystrophy, juvenile form Metachromatic leukodystrophy, late infantile form Mild Canavan disease Miller Fisher syndrome Myasthenia gravis Nasu-Hakola disease Neonatal adrenoleukodystrophy Null syndrome Odontoleukodystrophy Ovarioleukodystrophy Paraparetic variant of Guillain-Barré syndrome Pelizaeus-Merzbacher disease Pelizaeus-Merzbacher disease in female carriers Pelizaeus-Merzbacher disease, classic form Pelizaeus-Merzbacher disease, connatal form Pelizaeus-Merzbacher disease, transitional form Pelizaeus-Merzbacher-like disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Pelizaeus-Merzbacher-like disease due to GJC2 mutation Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Peroxisome biogenesis disorder Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome Progressive cavitating leukoencephalopathy Ravine syndrome Refsum disease Regional variant of Guillain-Barré syndrome Severe Canavan disease Spastic paraplegia type 2 Transient neonatal myasthenia gravis Unknown leukodystrophy Variant of Guillain-Barré syndrome X-linked adrenoleukodystrophy X-linked cerebral adrenoleukodystrophy Zellweger syndrome