{
    "disease_id": "DOID:0080077",
    "recommended_name": {
        "id": "DOID:0080077",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080077",
        "name": "hypophosphatemic nephrolithiasis/osteoporosis 1",
        "description": "A hypophosphatemic nephrolithiasis/osteoporosis that has_material_basis_in heterozygous mutation in the SLC34A1 gene on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "MONDO:0012850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012850",
            "name": "hypophosphatemic nephrolithiasis/osteoporosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0012850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012850",
            "name": "hypophosphatemic nephrolithiasis/osteoporosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012850",
            "name": "nephrolithiasis/osteoporosis, hypophosphatemic, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012850",
            "name": "NPHLOP1",
            "description": ""
        },
        {
            "id": "MONDO:0012850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012850",
            "name": "nephrolithiasis/osteoporosis, hypophosphatemic, 1",
            "description": ""
        },
        {
            "id": "MIM:612286",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612286",
            "name": "Nephrolithiasis/osteoporosis, hypophosphatemic, 1",
            "description": "Nephrolithiasis/osteoporosis, hypophosphatemic, 1"
        }
    ]
}