{
    "disease_id": "DOID:0080247",
    "recommended_name": {
        "id": "DOID:0080247",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080247",
        "name": "Galloway-Mowat syndrome 5",
        "description": "A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0033009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033009",
            "name": "Galloway-Mowat syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0033009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033009",
            "name": "Galloway-Mowat syndrome 5; GAMOS5",
            "description": ""
        },
        {
            "id": "MONDO:0033009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033009",
            "name": "GAMOS5",
            "description": ""
        },
        {
            "id": "MIM:617731",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617731",
            "name": "Galloway-Mowat syndrome 5",
            "description": "Galloway-Mowat syndrome 5"
        }
    ]
}