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