Disease Browser
Parent Node: Autoimmune Diseases of the Nervous System (D020274) Parent Node: Demyelinating Diseases (D003711) Parent Node: Leukoencephalopathies (D056784) ..Starting node .. Demyelinating Autoimmune Diseases, CNS (D020278) Child Nodes:
........Diffuse Cerebral Sclerosis of Schilder (D002549) 3 ........Encephalomyelitis, Acute Disseminated (D004673) ........Encephalomyelitis, Autoimmune, Experimental (D004681) ........Leukoencephalitis, Acute Hemorrhagic (D004684) 1 ........Multiple Sclerosis (D009103) 5 ........Myelitis, Transverse (D009188) 1 ........Neuromyelitis Optica (D009471) Sister Nodes: ..Ataxia, Spastic, 3, Autosomal Recessive (C566956) ..Brain Small Vessel Disease with Hemorrhage (C564372) ..Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (C563990) ..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401) ..Dementia, Vascular (D015140) 3 ..Demyelinating Autoimmune Diseases, CNS (D020278) 15 ..Gliosis, Familial Progressive Subcortical (C565634) ..Hereditary Central Nervous System Demyelinating Diseases (D020279) 29 ..Hereditary Diffuse Leukoencephalopathy with Spheroids (C580150) ..Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313) ..Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation (C567009) ..LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY (OMIM:613724) ..Leukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient (C566654) ..Leukoencephalopathy With Metaphyseal Chondrodysplasia (C567065) ..Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema (C563852) ..Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia (C535888) ..Leukoencephalopathy, Cystic, Without Megalencephaly (C567845) ..Leukoencephalopathy, Progressive Multifocal (D007968) ..Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy (C565361) ..Posterior Leukoencephalopathy Syndrome (D054038) ..Ribose 5-Phosphate Isomerase Deficiency (C563212) ..Telencephalic leukoencephalopathy (C536954) ..Vanishing White Matter Leukodystrophy with Ovarian Failure (C565836) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 3169
Name: Demyelinating Autoimmune Diseases, CNS
Definition: Conditions characterized by loss or dysfunction of myelin (see MYELIN SHEATH) in the brain, spinal cord, or optic nerves secondary to autoimmune mediated processes. This may take the form of a humoral or cellular immune response directed toward myelin or OLIGODENDROGLIA associated autoantigens.
Alternative IDs:
ParentIDs: MESH:D003711|MESH:D020274|MESH:D056784
TreeNumbers: C10.114.375 |C10.228.140.695.562 |C10.314.350 |C20.111.258.250
Synonyms: Autoimmune Demyelinating Diseases, Central Nervous System |Autoimmune Demyelinating Diseases, Cerebral |Autoimmune Demyelinating Diseases, CNS |Autoimmune Demyelinating Diseases, Spinal Cord |Autoimmune Demyelinating Disorders, CNS |Autoimmune Diseases, Demye
Slim Mappings: Immune system disease|Nervous system disease
Reference:
MedGen: D020278
MeSH: D020278
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants