{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110663", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110663", 
            "name": "CMS IIa"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110663", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110663", 
            "name": "CMS1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110663", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110663", 
            "name": "congenital myasthenic syndrome 1A, slow-channel"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110663", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110663", 
            "name": "congenital myasthenic syndrome type IIa"
        }, 
        {
            "url": "https://www.omim.org/entry/601462", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601462", 
            "name": "Myasthenic syndrome, congenital, 1A, slow-channel"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110663", 
        "description": "A congenital myasthenic syndrome characterized by predominantly autosomal dominant inheritance of defects in postsynaptic neuromuscular junctions and early-onset progressive muscle weakness that has_material_basis_in mutation in the CHRNA1 gene on chromosome 2q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110663", 
        "name": "congenital myasthenic syndrome 1A"
    }
}