{
    "disease_id": "DOID:0050699", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010359", 
            "name": "Dent disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010359", 
            "name": "nephrolithiasis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010359", 
            "name": "DENT disease 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010359", 
            "name": "Dent disease caused by mutation in OCRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010359", 
            "name": "OCRL Dent disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050699", 
            "name": "Dent disease 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050699", 
            "name": "Dent disease 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050699", 
            "name": "Dent's disease"
        }, 
        {
            "url": "https://www.omim.org/entry/300555", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300555", 
            "name": "Dent disease 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050699", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050699", 
        "name": "Dent disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300555", 
            "id": "300555", 
            "database": "MIM"
        }
    ]
}