{
    "disease_id": "DOID:0112014", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112014", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112014", 
            "name": "MGBL"
        }, 
        {
            "url": "https://www.omim.org/entry/618719", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618719", 
            "name": "Megabladder, congenital"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112014", 
        "description": "A bladder disease characterized by a massively dilated urinary bladder with disruption of the smooth muscle in the wall of the bladder that has_material_basis_in heterozygous mutation in MYOCD on chromosome 17p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112014", 
        "name": "congenital megabladder"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618719", 
            "id": "618719", 
            "database": "MIM"
        }
    ]
}
