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| Term | Lambert-Eaton myasthenic syndrome | ID (Ontology) | DOID:0050214 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "Eaton-Lambert syndrome" ; "Lambert-Eaton syndrome" ; "LEMS" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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musculoskeletal system disease |__autoimmune disease of musculoskeletal system_____ autoimmune disease | |__autoimmune disease of musculoskeletal system_____| autoimmune disease of the nervous system | |__autoimmune disease of peripheral nervous system__| neuromuscular disease | |__neuromuscular junction disease___________________| peripheral nervous system disease | |__autoimmune disease of peripheral nervous system__| Lambert-Eaton myasthenic syndrome |
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autoimmune disease of musculoskeletal system autoimmune disease of peripheral nervous system neuromuscular junction disease |
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ICD10CM:G70.80 ICD9CM:358.3 MESH:D015624 NCI:C3155 SNOMEDCT_US_2023_03_01:230688006 UMLS_CUI:C0022972 |
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