{
    "disease_id": "DOID:0111682", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011037", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011037", 
            "name": "renal dysplasia, cystic, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011037", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011037", 
            "name": "renal dysplasia, cystic, susceptibility to; CYSRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011037", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011037", 
            "name": "CYSRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011037", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011037", 
            "name": "renal dysplasia diffuse cystic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111682", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111682", 
            "name": "CYSRD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111682", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111682", 
            "name": "renal dysplasia diffuse cystic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111682", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111682", 
            "name": "susceptibility to cystic renal dysplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111682", 
        "description": "A cystic kidney disease characterized by nonsyndromic diffuse cystic dysplasia of the kidneys that has_material_basis_in heterozygous mutation in BICC1 on chromosome 10q21.1. The same mutation maybe found in unaffected parents suggesting incomplete penetrance of the disorder or that additional environmental factors are required for development of the disorder.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111682", 
        "name": "diffuse cystic renal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111682#disease-associations", 
            "id": "0111682", 
            "database": "Alliance of Genome Resources"
        }
    ]
}