{
    "disease_id": "DOID:0111114", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "Nph3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "NPHP3 nephronophthisis (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "nephronophthisis type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "NPHP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "nephronophthisis (disease) caused by mutation in NPHP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011456", 
            "name": "nephronophthisis 3; NPHP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111114", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111114", 
            "name": "NPH3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111114", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111114", 
            "name": "NPHP3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111114", 
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the NPHP3 gene on chromosome 3q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111114", 
        "name": "nephronophthisis 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111114#disease-associations", 
            "id": "0111114", 
            "database": "Alliance of Genome Resources"
        }
    ]
}