• 18q Syndrome
  • Acute Disseminated Encephalomyeolitis (ADEM)
  • Acute Disseminated Leukoencephalitis
  • Acute Hemorrhagic Leukoencephalopathy
  • Adrenoleukodystrophy (ALD)
  • Adrenomyeloneuropathy (AMN)
  • Adult Onset Autosomal Dominant Leukodystrophy (ADLD)
  • Adult Polyglucosan Body Disease
  • Aicardi-Goutieres Syndrome
  • Alexander Disease
  • Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids (HDLS)
  • Autosomal Dominant Late-Onset Leukoencephalopathy
  • Canavan Disease
  • Cerebrotendinous Xanthomatosis (CTX)
  • Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
  • Cerebroretinal Micro-Angiography with Calcifications and Cysts
  • Childhood Ataxia with Central Nervous System Hypomyelination (CACH)
  • Childhood Ataxia with Diffuse CNS Hypomyelination (CACH or Vanishing White Matter Disease)
  • Craniometaphysical Dysplasia with Leukoencephalopathy
  • Cystic Leukoencephalopathy (RNASET2 related)
  • Elongation of Very Long-Chain Fatty Acids-4 (ELOVL4; Pseudo-Sjogren-Larsson)
  • Extensive Cerebral White Matter Abnormality without Clinical Symptoms
  • Familial Adult-Onset Leukodystrophy Manifesting as Cerebellar Ataxia and Dementia
  • Familial Leukodystrophy with Adult Onset Dementia and Abnormal Glycolipid Storage
  • Fatty Acid 2-Hydroxylase Deficiency
  • Fucosidosis
  • Fukuyama Congential Muscular Dystrophy
  • Galactosialidosis
  • Globoid Cell Leukodystrophy (Krabbe Disease)
  • GM1 Gangliosidosis
  • GM2 Gangliosidosis (Tay-Sachs Disease)
  • Hereditary Adult Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
  • Herditary Diffuse Leukoencephalopathy with Axonal Spheroids (HDLS)
  • Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC)
  • Hypomyelination, Hypogonadotropic, Hypogonadism and Hypodontia (4H Syndrome)
  • Infantile Refsum Disease
  • Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL)
  • Lipomembranous Osteodysplasia with Leukodystrophy (Nasu Disease)
  • Metachromatic Leukodystrophy (MLD)
  • Megalencephalic Leukodystrophy with subcortical Cysts (MLC)
  • Neuroaxonal Leukoencephalopathy
  • Neonatal Adrenoleukodystrophy (NALD)
  • Oculodetatoldigital Dysplasia with Cerebral White Matter Abnormalities
  • Orthochromatic Leukodystrophy with Pigmented Glia
  • Ovarioleukodystrophy Syndrome
  • Pelizaeus Merzbacher Disease
  • Refsum Disease
  • Sjogren-Larsson Syndrome
  • Sudanophilic Leukodystrophy
  • Van der Knaap Syndrome
  • Vanishing White Matter Disease (VWM)
  • X-linked Adrenoleukodystrophy (X-ALD)
  • Zellweger Syndrome

Visit the United Leukodystrophy Foundation for more information.