{
    "disease_id": "DOID:0050214", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0050214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050214", 
            "name": "Eaton-Lambert syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050214", 
            "name": "LEMS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050214", 
            "name": "Lambert-Eaton syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050214", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050214", 
        "name": "Lambert-Eaton myasthenic syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050214#disease-associations", 
            "id": "0050214", 
            "database": "Alliance of Genome Resources"
        }
    ]
}