Lambert-Eaton Myasthenic Syndrome
Disease ID: disease_node_8398
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G70.80, ICD9CM:358.3, MESH:D015624, NCI:C3155, SNOMEDCT_US_2023_03_01:230688006, UMLS_CUI:C0022972 |
|---|---|
| Subclassof | DOID_0060033, DOID_439, DOID_0060032 |
| Data Source | DOID, MESH |
| Synonyms | Eaton-Lambert syndrome, LEMS, Lambert-Eaton syndrome |
| Mesh Id | D015624 |
| Mesh Label | Lambert-Eaton Myasthenic Syndrome |
| Mesh Subclassof | D009157 |
| Doid Label | Lambert-Eaton myasthenic syndrome |
| Doid Description | 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. |
| Has Phenotype | HP_0010701 |
| Disease Node Id | disease_node_8398 |
| Doid Id | DOID_0050214 |
| Label | Lambert-Eaton Myasthenic Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Neuromuscular Junction Diseases(ID:disease_node_10604) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autoimmune Disease Of Musculoskeletal System(ID:disease_node_13172) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autoimmune Disease Of Peripheral Nervous System(ID:disease_node_14243) (Disease)