{
    "disease_id": "DOID:0111113",
    "recommended_name": {
        "id": "DOID:0111113",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111113",
        "name": "nephronophthisis 2",
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the INVS gene on chromosome 9q31."
    },
    "synonyms": [
        {
            "id": "DOID:0111113",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111113",
            "name": "NPH2",
            "description": ""
        },
        {
            "id": "DOID:0111113",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111113",
            "name": "NPHP2",
            "description": ""
        },
        {
            "id": "DOID:0111113",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111113",
            "name": "infantile nephronophthisis 2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "nephronophthisis 2",
            "description": "Any nephronophthisis in which the cause of the disease is a mutation in the INVS gene."
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "INVS nephronophthisis (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "nephronophthisis 2; NPHP2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "NPH2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "nephronophthisis 2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "Nph2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "nephronophthisis (disease) caused by mutation in INVS",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "infantile nephronophthisis 2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "NPHP2",
            "description": ""
        },
        {
            "id": "MONDO:0011190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011190",
            "name": "nephronophthisis type 2",
            "description": ""
        },
        {
            "id": "MIM:602088",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602088",
            "name": "Nephronophthisis 2",
            "description": "Nephronophthisis 2"
        }
    ]
}