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:
expandPolyneuropathies (D011115)
..Starting node
..expandPolyradiculoneuropathy (D011129)

       Child Nodes:
........expandGuillain-Barre Syndrome (D020275) Child1
........expandHereditary Sensory and Autonomic Neuropathies (D009477) Child12
........expandPolyradiculoneuropathy, Chronic Inflammatory Demyelinating (D020277)
........expandPolyradiculopathy (D011128)
........expandRadiculoneuropathy, Fatal Neonatal (C564857)



 Sister Nodes: 
..expand46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy (C567773)
..expandAlcoholic Neuropathy (D020269)
..expandAplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy (C565945)
..expandAtaxia and Polyneuropathy, Adult-Onset (C564020)
..expandDeafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease (C565120)
..expandHereditary Sensory and Autonomic Neuropathies (D009477) Child12
..expandHereditary Sensory and Motor Neuropathy (D015417) Child164
..expandLaryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy (C565252)
..expandLEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY (OMIM:613724)
..expandLeukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient (C566654)
..expandNeuropathy, Hereditary Sensory, Atypical (C564946)
..expandOptic atrophy polyneuropathy deafness (C537129)
..expandParaneoplastic Polyneuropathy (D020364)
..expandPeripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease (C563789)
..expandPOEMS Syndrome (D016878)
..expandPolyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
..expandPolyradiculoneuropathy (D011129) Child18
..expandRibose 5-Phosphate Isomerase Deficiency (C563212)
..expandSevere infantile axonal neuropathy (C537593)
..expandTangier Disease (D013631)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9114
Name:Polyradiculoneuropathy
Definition:Diseases characterized by injury or dysfunction involving multiple peripheral nerves and nerve roots. The process may primarily affect myelin or nerve axons. Two of the more common demyelinating forms are acute inflammatory polyradiculopathy (GUILLAIN-BARRE SYNDROME) and POLYRADICULONEUROPATHY, CHRONIC INFLAMMATORY DEMYELINATING. Polyradiculoneuritis refers to inflammation of multiple peripheral nerves and spinal nerve roots.
Alternative IDs:
ParentIDs:MESH:D003711|MESH:D011115|MESH:D020274
TreeNumbers:C10.114.750 |C10.314.750 |C10.668.829.800.750 |C20.111.258.750
Synonyms:Autoimmune Demyelinating Disease, Peripheral |Demyelinating Autoimmune Disease, Peripheral |Demyelinating Disease, Peripheral Autoimmune |Peripheral Autoimmune Demyelinating Disease |Polyradiculoneuritides |Polyradiculoneuritis |Polyradiculoneuropathies
Slim Mappings:Immune system disease|Nervous system disease
Reference: MedGen: D011129
MeSH: D011129
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants