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Ontology Browser

Term:
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 +   
Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord.
Chronobiology Disorders +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital nervous system abnormality +   
diplegia of upper limb 
Gerstmann syndrome 
herpes zoster +   
hyperekplexia +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
MEND SYNDROME  
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
neurogenic arthrogryposis multiplex congenita +   
Neurologic Manifestations +   
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET  
neuronal intestinal dysplasia  
Norrie disease  
peripheral nervous system disease +   
Polyglucosan Body Disease, Adult Form  
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   
Trauma, Nervous System +   

Synonyms
Exact Synonyms: CNS Disease ;   CNS Diseases ;   Central Nervous System Disorders ;   central nervous system diseases
Primary IDs: MESH:D002493 ;   RDO:0000677
Xrefs: NCI:C2934
Definition Sources: MESH:D002493, http://en.wikipedia.org/wiki/Central_nervous_system_disease

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