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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
autoimmune disease of central nervous system +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
brain disease +   
cardiac sarcoidosis 
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
Early-Onset Sarcoidosis +   
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
Flynn Aird Syndrome 
hemiplegia +   
high pressure neurological syndrome 
hypercalcemic sarcoidosis 
hyperekplexia +   
intracranial abscess 
maturity-onset diabetes of the young type 5  
meningitis +   
meningoencephalitis +   
movement disease +   
neurodegenerative disease +   
neuronitis 
neurosarcoidosis +  
A sarcoidosis that is characterized by involvement of the nervous symptom with cranial nerve palsy, diffuse meningeal disease, acute polyneuropathy, myelitis, or hypothalamic pituitary axis malformation, develops_from a type IV hypersensitivity reaction with noncaseating granulomas involving the nervous system. (DO)
ocular motility disease +   
paraplegia +   
Pneumocephalus 
pulmonary sarcoidosis  
quadriplegia +   
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal  
skin sarcoidosis 
spinal cord disease +   
uveoparotid fever  

Synonyms
Exact Synonyms: Nervous system sarcoidosis ;   cerebral sarcoidosis
Primary IDs: MESH:C535814
Xrefs: NCI:C35441
Definition Sources: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975794/ "DO" "DO"

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