{
    "disease_id": "DOID:0080245", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033007", 
            "name": "GAMOS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033007", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033007", 
            "name": "Galloway-Mowat syndrome 3; GAMOS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080245", 
        "description": "A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080245", 
        "name": "Galloway-Mowat syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617729", 
            "id": "617729", 
            "database": "MIM"
        }
    ]
}