{
    "disease_id": "DOID:0110666", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014583", 
            "name": "congenital myasthenic syndrome 3A, slow-channel"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014583", 
            "name": "myasthenic syndrome, congenital, 3A, slow-channel"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014583", 
            "name": "congenital myasthenic syndrome type 3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014583", 
            "name": "CMS3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014583", 
            "name": "myasthenic syndrome, congenital, 3A, slow-channel; CMS3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110666", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110666", 
            "name": "CMS3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110666", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110666", 
            "name": "congenital myasthenic syndrome 3A, slow-channel"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110666", 
        "description": "A congenital myasthenic syndrome characterized by autosomal dominant inheritance of postsynaptic neuromuscular junction defects resulting in prolonged synaptic currents and early-onset progressive muscle weakness that has_material_basis_in heterozygous mutation in the CHRND gene on chromosome 2q37.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110666", 
        "name": "congenital myasthenic syndrome 3A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110666#disease-associations", 
            "id": "0110666", 
            "database": "Alliance of Genome Resources"
        }
    ]
}