{
    "disease_id": "DOID:0111118", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013302", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013302", 
            "name": "nephronophthisis type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013302", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013302", 
            "name": "NPHP11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013302", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013302", 
            "name": "nephronophthisis 11; NPHP11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111118", 
            "name": "NPHP11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111118", 
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111118", 
        "name": "nephronophthisis 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111118#disease-associations", 
            "id": "0111118", 
            "database": "Alliance of Genome Resources"
        }
    ]
}