{
    "disease_id": "DOID:0080652",
    "recommended_name": {
        "id": "DOID:0080652",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080652",
        "name": "calcium oxalate nephrolithiasis",
        "description": "A nephrolithiasis that is characterized by characterized by stones composed of calcium oxalate and that has_material_basis_in compound heterozygous mutation in the SLC26A1 gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "MONDO:0020722",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020722",
            "name": "nephrolithiasis susceptibility caused by SLC26A1",
            "description": ""
        },
        {
            "id": "MONDO:0020722",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020722",
            "name": "CAON",
            "description": ""
        },
        {
            "id": "MONDO:0020722",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020722",
            "name": "nephrolithiasis, calcium oxalate",
            "description": ""
        },
        {
            "id": "MONDO:0020722",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020722",
            "name": "urolithiasis, calcium oxalate",
            "description": ""
        },
        {
            "id": "MIM:167030",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/167030",
            "name": "Nephrolithiasis, calcium oxalate, 1",
            "description": "Nephrolithiasis, calcium oxalate, 1"
        }
    ]
}
