{
    "disease_id": "DOID:0081453",
    "recommended_name": {
        "id": "DOID:0081453",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081453",
        "name": "Dent disease 1",
        "description": "A Dent disease that is characterized by manifestations of complex proximal tubule dysfunction with low-molecular-weight proteinuria, hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure and that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11. Extra-renal involvement is absent."
    },
    "synonyms": [
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "Dent disease type 1",
            "description": "Dent disease type 1 is a type of Dent disease with predominantly renal manifestations."
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "CLCN5 Dent disease",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "Dent disease caused by mutation in CLCN5",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "Dent disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "dent disease 1, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "nephrolithiasis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "DENT disease 1",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "nephrolithiasis 2",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "nephrolithiasis, hypercalciuric, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "urolithiasis, hypercalciuric, X-linked",
            "description": ""
        },
        {
            "id": "MIM:300009",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300009",
            "name": "Dent disease 1",
            "description": "Dent disease 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081453"
    ],
    "unlinked_id_list": []
}