{
    "disease_id": "DOID:0111815", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010644", 
            "name": "proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111815", 
        "description": "A Dent disease characterized by elevted levels of low molecular weight proteins in the urine, hypercalciuria, and nephrocalcinosis that has_material_basis_in hemizygous or homozygous mutation in CLCN5 on chromosome Xp11.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111815", 
        "name": "low molecular weight proteinuria with hypercalciuric nephrocalcinosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111815#disease-associations", 
            "id": "0111815", 
            "database": "Alliance of Genome Resources"
        }
    ]
}