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Diseases

Lambert-Eaton Myasthenic Syndrome

lambert-eaton myasthenic syndrome

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Lambert-Eaton Myasthenic Syndrome
Standard Disease Name
lambert-eaton myasthenic syndrome
MeSH Tree
No data
ICD-10
G70.80

Identifiers

DO ID
No data
MeSH ID
D015624
OMIM ID
No data
UMLS ID
C0022972
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A rare autoimmune presynaptic disorder characterized by impairment of the impulse transmission at the neuromuscular junction. It affects predominantly the proximal muscles of the lower extremities, resulting in muscle weakness and fatigability. It has been associated with small cell lung carcinoma.|MSH2017_2016_08_12:An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471)
Related

Direct relations and traceable candidates grouped by relation type.

Candidate Herbs

target disease -> ingredient target -> herb ingredient8 Herbs