{
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "congenital myasthenic syndrome 8 with pre- and postsynaptic defects"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "myasthenic syndrome, congenital, 8; CMS8"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "congenital myasthenic syndrome due to agrin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "congenital myasthenic syndrome caused by mutation in AGRN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "myasthenic syndrome, congenital, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "myasthenic syndrome, congenital, due to agrin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014052", 
            "name": "CMS8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110657", 
            "name": "congenital myasthenic syndrome 8 with pre- and postsynaptic defects"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "CMS8"
        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110657", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615120", 
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        }
    ], 
    "recommended_name": {
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        "description": "A congenital myasthenic syndrome characterized by autosomal recessive inheritance of prominent defects of both the pre- and postsynaptic regions and muscle weakness that has_material_basis_in homozygous or compound heterozygous mutation in the AGRN gene on chromosome 1p.", 
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    }, 
    "evidence": [
        {
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            "id": "615120", 
            "database": "MIM"
        }
    ]
}