{
    "disease_id": "DOID:0061293",
    "recommended_name": {
        "id": "DOID:0061293",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061293",
        "name": "Galloway-Mowat syndrome 10",
        "description": "A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34."
    },
    "synonyms": [
        {
            "id": "MONDO:0030476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030476",
            "name": "Galloway-Mowat syndrome 10",
            "description": ""
        },
        {
            "id": "MONDO:0030476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030476",
            "name": "GAMOS10",
            "description": ""
        },
        {
            "id": "MIM:619609",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619609",
            "name": "Galloway-Mowat syndrome 10",
            "description": "Galloway-Mowat syndrome 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061293"
    ],
    "unlinked_id_list": []
}