{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "myasthenic syndrome, congenital, 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "congenital myasthenic syndrome type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "ALG14 congenital myasthenic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "CMS15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "congenital myasthenic syndrome 15 without tubular aggregates"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "congenital myasthenic syndrome caused by mutation in ALG14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "myasthenic syndrome, congenital, 15; CMS15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "myasthenic syndrome, congenital, type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014542", 
            "name": "myasthenic syndrome, congenital, without tubular aggregates"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110658", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110658", 
            "name": "CMS15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110658", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110658", 
            "name": "congenital myasthenic syndrome 15 without tubular aggregates"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110658", 
        "description": "A congenital myasthenic syndrome characterized by onset of progressive fatigable proximal muscle weakness in childhood that has_material_basis_in compound heterozygous mutation in the ALG14 gene on chromosome 1p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110658", 
        "name": "congenital myasthenic syndrome 15"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014542", 
            "id": "0014542", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/616227", 
            "id": "616227", 
            "database": "MIM"
        }
    ]
}