Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandAutoimmune Diseases of the Nervous System (D020274)
Parent Node:
expandDemyelinating Diseases (D003711)
Parent Node:
expandLeukoencephalopathies (D056784)
..Starting node
..expandDemyelinating Autoimmune Diseases, CNS (D020278)

       Child Nodes:
........expandDiffuse Cerebral Sclerosis of Schilder (D002549) Child3
........expandEncephalomyelitis, Acute Disseminated (D004673)
........expandEncephalomyelitis, Autoimmune, Experimental (D004681)
........expandLeukoencephalitis, Acute Hemorrhagic (D004684) Child1
........expandMultiple Sclerosis (D009103) Child5
........expandMyelitis, Transverse (D009188) Child1
........expandNeuromyelitis Optica (D009471)



 Sister Nodes: 
..expandAtaxia, Spastic, 3, Autosomal Recessive (C566956)
..expandBrain Small Vessel Disease with Hemorrhage (C564372)
..expandCerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (C563990)
..expandCerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
..expandDementia, Vascular (D015140) Child3
..expandDemyelinating Autoimmune Diseases, CNS (D020278) Child15
..expandGliosis, Familial Progressive Subcortical (C565634)
..expandHereditary Central Nervous System Demyelinating Diseases (D020279) Child29
..expandHereditary Diffuse Leukoencephalopathy with Spheroids (C580150)
..expandLeukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
..expandLeukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation (C567009)
..expandLEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY (OMIM:613724)
..expandLeukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient (C566654)
..expandLeukoencephalopathy With Metaphyseal Chondrodysplasia (C567065)
..expandLeukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema (C563852)
..expandLeukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia (C535888)
..expandLeukoencephalopathy, Cystic, Without Megalencephaly (C567845)
..expandLeukoencephalopathy, Progressive Multifocal (D007968)
..expandMuscular Dystrophy, Adult-Onset, with Leukoencephalopathy (C565361)
..expandPosterior Leukoencephalopathy Syndrome (D054038)
..expandRibose 5-Phosphate Isomerase Deficiency (C563212)
..expandTelencephalic leukoencephalopathy (C536954)
..expandVanishing 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