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:
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Nervous System Diseases (D009422)
..Starting node
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Demyelinating Diseases (D003711)

       Child Nodes:
........expandBoylan Dew Greco syndrome (C537083)
........expandCAMFAK syndrome (C537965)
........expandDemyelinating Autoimmune Diseases, CNS (D020278) Child15
........expandGroll Hirschowitz syndrome (C537305)
........expandHamano Tsukamoto syndrome (C535625)
........expandHereditary Central Nervous System Demyelinating Diseases (D020279) Child29
........expandHypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response (C537159)
........expandLeukoencephalopathy, Progressive Multifocal (D007968)
........expandMarchiafava-Bignami Disease (D054319)
........expandMyelinolysis, Central Pontine (D017590)
........expandOphthalmoplegic Migraine (D060486)
........expandPolyradiculoneuropathy (D011129) Child18
........expandSubacute Combined Degeneration (D052879)



 Sister Nodes: 
..expandAlpha-Methylacyl-CoA Racemase Deficiency (C565768)
..expandAutoimmune Diseases of the Nervous System (D020274) Child60
..expandAutonomic Nervous System Diseases (D001342) Child51
..expandCentral Nervous System Diseases (D002493) Child1489
..expandChronobiology Disorders (D021081) Child5
..expandCongenital Cataracts, Facial Dysmorphism, And Neuropathy (C565822)
..expandCranial Nerve Diseases (D003389) Child238
..expandDemyelinating Diseases (D003711) Child75
..expandMarcus Gunn phenomenon (C535908)
..expandNervous System Malformations (D009421) Child567
..expandNervous System Neoplasms (D009423) Child89
..expandNeurocutaneous Syndromes (D020752) Child42
..expandNeurodegenerative Diseases (D019636) Child704
..expandNeurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954)
..expandNeurologic Manifestations (D009461) Child1586
..expandNeuromuscular Diseases (D009468) Child811
..expandNeuronal intestinal pseudoobstruction (C537394)
..expandNeurotoxicity Syndromes (D020258) Child20
..expandNorrie disease (C537849)
..expandPolyglucosan Body Disease, Adult Form (C564878)
..expandRestless Legs Syndrome (D012148) Child2
..expandRoy Maroteaux Kremp syndrome (C535875)
..expandSleep Disorders (D012893) Child41
..expandTang Hsi Ryu syndrome (C536897)
..expandTrauma, Nervous System (D020196) Child73
..expandTrifunctional Protein Deficiency With Myopathy And Neuropathy (C566945)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:3170
Name:Demyelinating Diseases
Definition:Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system.
Alternative IDs:
ParentIDs:MESH:D009422
TreeNumbers:C10.314
Synonyms:Clinically Isolated CNS Demyelinating Syndrome |Clinically Isolated Syndrome, CNS Demyelinating |Demyelinating Disease |Demyelinating Disorder |Demyelinating Disorders |Demyelination |Demyelinations
Slim Mappings:Nervous system disease
Reference: MedGen: D003711
MeSH: D003711
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants