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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 nervous system disease characterized by an exaggerated startle response to sudden, unexpected auditory or tactile stimuli and hypertonia. (DO)
intracranial abscess 
maturity-onset diabetes of the young type 5  
meningitis +   
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: Kok disease ;   STHE ;   congenital stiff man syndrome ;   exagerrated startle reflex ;   exaggerated startle reaction ;   hyperekplexias ;   startle disease
Primary IDs: MESH:D000071017
Alternate IDs: OMIA:001594
Xrefs: GARD:3129 ;   OMIM:PS149400
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12427512 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/1334371 "DO" "DO"

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