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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Accessory Deep Peroneal Nerve 
Acrodynia 
agenesis of the corpus callosum with peripheral neuropathy  
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
Cataract Ataxia Deafness 
Cauda equina syndrome 
complex regional pain syndrome +  
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
diabetic neuropathy +   
Gamstorp-Wohlfart syndrome  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hypertrophic Neuropathy and Cataract 
Inherited Peripheral Neuropathy  
leprosy +   
lumbosacral plexus lesion 
mitochondrial DNA depletion syndrome 6  
mononeuropathy +   
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuropathy +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Painful Neuropathy  
Peripheral Nerve Injuries  
peripheral nervous system neoplasm +   
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polyneuropathy +   
Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance.
radiculopathy  
Sacral Plexopathy 
Small Fiber Neuropathy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
Tarlov Cysts 

Synonyms
Exact Synonyms: Acquired Polyneuropathies ;   Acquired Polyneuropathy ;   Critical Illness Polyneuropathies ;   Critical Illness Polyneuropathy ;   Familial Polyneuropathies ;   Familial Polyneuropathy ;   Inherited Polyneuropathies ;   Inherited Polyneuropathy ;   Motor Polyneuropathies ;   Motor Polyneuropathy ;   multifocal motor neuropathy ;   polyneuropathies
Primary IDs: MESH:D011115 ;   RDO:0001222
Alternate IDs: OMIA:001292
Xrefs: ICD10CM:G62.9 ;   NCI:C26951
Definition Sources: MESH:D011115, https://en.wikipedia.org/wiki/Polyneuropathy, https://www.virginiamason.org/polyneuropathy

paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.