{
    "disease_id": "DOID:0110662", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012156", 
            "name": "myasthenic syndrome, congenital, 1B, fast-channel"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012156", 
            "name": "CMS1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012156", 
            "name": "congenital myasthenic syndrome 1B, fast-channel"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012156", 
            "name": "congenital myasthenic syndrome type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012156", 
            "name": "myasthenic syndrome, congenital, 1B, FAST-channel; CMS1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110662", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110662", 
            "name": "CMS1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110662", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110662", 
            "name": "congenital myasthenic syndrome 1B, fast-channel"
        }, 
        {
            "url": "https://www.omim.org/entry/608930", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608930", 
            "name": "Myasthenic syndrome, congenital, 1B, fast-channel"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110662", 
        "description": "A congenital myasthenic syndrome characterized by defects in postsynaptic neuromuscular junctions with early-onset progressive muscle weakness that has_material_basis_in mutation in the CHRNA1 gene on chromosome 2q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110662", 
        "name": "congenital myasthenic syndrome 1B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608930", 
            "id": "608930", 
            "database": "MIM"
        }
    ]
}