{
    "disease_id": "DOID:0050699",
    "recommended_name": {
        "id": "DOID:0050699",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050699",
        "name": "Dent disease",
        "description": "A renal tubular transport disease that is characterized by  tubular proteinuria, hypercalciuria, calcium nephrolithiasis, nephrocalcinosis and chronic kidney failure and has_material_basis_in X-linked recessive inheritance of mutations in the CLCN5 gene or OCRL1 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050699",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050699",
            "name": "Dent disease 1",
            "description": ""
        },
        {
            "id": "DOID:0050699",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050699",
            "name": "Dent disease 2",
            "description": ""
        },
        {
            "id": "DOID:0050699",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050699",
            "name": "Dent's disease",
            "description": ""
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "Dent disease type 2",
            "description": "Dent disease type 2 is a type of Dent disease in which patients have the manifestations of Dent disease type 1 (see this term) associated with extra-renal features."
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "nephrolithiasis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "DENT disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "Dent disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "Dent disease caused by mutation in OCRL",
            "description": ""
        },
        {
            "id": "MONDO:0010359",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010359",
            "name": "OCRL Dent disease",
            "description": ""
        },
        {
            "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 (see this term) with predominantly renal manifestations."
        },
        {
            "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": "CLCN5 Dent disease",
            "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": "Dent disease caused by mutation in CLCN5",
            "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": "nephrolithiasis 2",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "urolithiasis, hypercalciuric, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010225",
            "name": "DENT disease 1",
            "description": ""
        },
        {
            "id": "MIM:300555",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300555",
            "name": "Dent disease 2",
            "description": "Dent disease 2"
        },
        {
            "id": "MIM:300009",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300009",
            "name": "Dent disease 1",
            "description": "Dent disease 1"
        }
    ]
}