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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
ankylosing spondylitis +   
Anti-N-Methyl-D-Aspartate Receptor Encephalitis  
autoimmune disease of skin and connective tissue +   
autoimmune optic neuritis  
autoimmune peripheral neuropathy 
botulism +  
chronic inflammatory demyelinating polyradiculoneuropathy  
congenital myasthenic syndrome +   
Guillain-Barre syndrome +   
juvenile ankylosing spondylitis 
Lambert-Eaton myasthenic syndrome  
A neuromuscular junction disease that is characterized by an abnormality of acetylcholine (ACh) release at the neuromuscular junction which results from an autoimmune attack against voltage-gated calcium channels (VGCC) on the presynaptic motor nerve terminal. (DO)
limbic encephalitis 
lupus erythematosus +   
mixed connective tissue disease  
myasthenia gravis +   
neuromyelitis optica  
Opsoclonus-Myoclonus Syndrome +   
Paraneoplastic Cerebellar Degeneration 
paraneoplastic polyneuropathy 
polymyositis +   
reactive arthritis  
relapsing polychondritis +   
rheumatic disease +   
rheumatoid arthritis interstitial lung disease 
transverse myelitis +   

Synonyms
Exact Synonyms: Eaton Lambert Syndrome ;   Eaton-Lambert Myasthenic-Myopathic Syndrome ;   Eaton-Lambert Myopathic-Myasthenic Syndromes ;   LEMS ;   myasthenic-myopathic syndrome of Eaton Lambert
Primary IDs: MESH:D015624
Xrefs: ICD10CM:G70.80 ;   ICD9CM:358.3 ;   NCI:C3155
Definition Sources: http://en.wikipedia.org/wiki/Lambert%E2%80%93Eaton_myasthenic_syndrome "DO" "DO"

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