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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 +   
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
Flynn Aird Syndrome 
hemiplegia +   
high pressure neurological syndrome 
hyperekplexia +   
A neurological disorder characterized by an excessive startle reaction with ABNORMAL REFLEX; MYOCLONIC JERKS; and MUSCLE HYPERTONIA.
intracranial abscess 
maturity-onset diabetes of the young type 5  
meningitis +   
meningoencephalitis +   
movement disease +   
neurodegenerative disease +   
neuronitis 
neurosarcoidosis +  
ocular motility disease +   
paraplegia +   
Pneumocephalus 
Progressive Encephalomyelitis with Rigidity 
quadriplegia +   
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal 
spinal cord disease +   
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 

Synonyms
Exact Synonyms: Hyperekplexias ;   Kok disease ;   STHE ;   congenital stiff man syndrome ;   exagerrated startle reflex ;   exaggerated startle reaction ;   startle disease
Primary IDs: MESH:D000071017
Alternate IDs: OMIA:001594
Xrefs: OMIM:PS149400
Definition Sources: MESH:D000071017, https://www.ncbi.nlm.nih.gov/pubmed/12427512, https://www.ncbi.nlm.nih.gov/pubmed/1334371

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