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Ontology Browser

Parent Terms Term With Siblings Child Terms
alpha-methylacyl-CoA racemase deficiency  
autoimmune disease of the nervous system +   
autonomic nervous system disease +   
central nervous system disease +   
Chronobiology Disorders +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital nervous system abnormality +   
diplegia of upper limb 
Gerstmann syndrome 
herpes zoster +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
MEND Syndrome  
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Nervous System Trauma +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
neurogenic arthrogryposis multiplex congenita +   
Neurologic Manifestations +   
neuronal intestinal dysplasia  
Norrie disease  
peripheral nervous system disease +   
Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves.
Polyglucosan Body Disease, Adult Form  
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   
 leprosy +   
 mononeuropathy +   
 Neuralgia +   
 neuritis +   
 neuropathy +   
 polyneuropathy +   
 radiculopathy +   

Exact Synonyms: PNS (Peripheral Nervous System) Diseases ;   PNS Disease ;   PNS Diseases ;   Peripheral Nerve Disease ;   Peripheral Nerve Diseases ;   Peripheral Nervous System Disorders ;   Peripheral Neuropathies ;   Peripheral Neuropathy ;   peripheral nervous system diseases
Primary IDs: MESH:D010523 ;   RDO:0001405
Xrefs: ICD10CM:G64 ;   ICD9CM:350-359.99 ;   NCI:C119734 ;   NCI:C27580 ;   NCI:C27587
Definition Sources: MESH:D010523,

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