SE-ATLAS

Neonatal adrenoleukodystrophy Unknown leukodystrophy Cystic leukoencephalopathy without megalencephaly Pelizaeus-Merzbacher-like disease due to GJC2 mutation CADDS Late infantile CACH syndrome Hypomyelination with brain stem and spinal cord involvement and leg spasticity Ravine syndrome Congenital or early infantile CACH syndrome Alexander disease type II Severe Canavan disease Spastic paraplegia type 2 Cree leukoencephalopathy Juvenile or adult CACH syndrome Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Ovarioleukodystrophy Peroxisome biogenesis disorder CACH syndrome Pelizaeus-Merzbacher disease, connatal form Leukoencephalopathy with bilateral anterior temporal lobe cysts Aicardi-Goutières syndrome Leukoencephalopathy-dystonia-motor neuropathy syndrome Hypomyelination with atrophy of basal ganglia and cerebellum Pelizaeus-Merzbacher disease in female carriers Metachromatic leukodystrophy Metachromatic leukodystrophy, juvenile form Alexander disease type I Late-infantile/juvenile Krabbe disease Progressive cavitating leukoencephalopathy X-linked cerebral adrenoleukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Metachromatic leukodystrophy, late infantile form Leukoencephalopathy with mild cerebellar ataxia and white matter edema Pelizaeus-Merzbacher disease Adult Krabbe disease Mild Canavan disease Pelizaeus-Merzbacher disease, transitional form Canavan disease Hypomyelination-congenital cataract syndrome Infantile Refsum disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Cerebrotendinous xanthomatosis Null syndrome Refsum disease Leukodystrophy Megalencephalic leukoencephalopathy with subcortical cysts Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Adult-onset autosomal dominant leukodystrophy Alexander-Krankheit Krabbe-Syndrom, infantile Form Pelizaeus-Merzbacher-ähnliche Krankheit Pelizaeus-Merzbacher-Krankheit, klassische Form Leukodystrophie, metachromatische, adulte Form Allan-Herndon-Dudley-Syndrom 4H-Leukodystrophie Nasu-Hakola-Krankheit Pelizaeus-Merzbacher-ähnliche Krankheit mit HSPD1-Genmutationen Enzephalopathie, frühkindliche myoklonische Zellweger-Syndrom Leukoenzephalopathie mit Hirnstamm- und Rückenmarkbeteiligung - Laktaterhöhung Adrenoleukodystrophie, X-chromosomale Adrenomyeloneuropathie Krabbe-Syndrom