{
    "disease_id": "DOID:0061292",
    "recommended_name": {
        "id": "DOID:0061292",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061292",
        "name": "Galloway-Mowat syndrome 9",
        "description": "A Galloway-Mowat syndrome characterized by onset of nephrotic syndrome with proteinuria in infancy or early childhood that has_material_basis_in homozygous mutation in the GON7 gene on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0030471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030471",
            "name": "Galloway-Mowat syndrome 9",
            "description": ""
        },
        {
            "id": "MONDO:0030471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030471",
            "name": "GAMOS9",
            "description": ""
        },
        {
            "id": "MIM:619603",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619603",
            "name": "Galloway-Mowat syndrome 9",
            "description": "Galloway-Mowat syndrome 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061292"
    ],
    "unlinked_id_list": []
}