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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 +   
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME  
central nervous system disease +   
A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. (DO)
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 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 1  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 2  
intestinal pseudo-obstruction +   
LETM1-ASSOCIATED CLINICAL SPECTRUM WITH PREDOMINANT NERVOUS SYSTEM INVOLVEMENT  
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Nervous System Trauma +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
Neurologic Manifestations +   
Norrie disease  
peripheral nervous system disease +   
Polyglucosan Body Disease, Adult Form  
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   

Synonyms
Exact Synonyms: CNS DISORDER ;   CNS Disease ;   CNS Diseases ;   Central Nervous System Disorders ;   central nervous system diseases
Primary IDs: MESH:D002493
Xrefs: EFO:0009386 ;   ICD10CM:G96.9 ;   NCI:C2934
Definition Sources: http://en.wikipedia.org/wiki/Central_nervous_system_disease "DO" "DO"

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