{
    "disease_id": "DOID:0051078",
    "recommended_name": {
        "id": "DOID:0051078",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051078",
        "name": "congenital anomalies of the kidney and urinary tract 3",
        "description": "A congenital anomalies of the kidney and urinary tract that has_material_basis_in heterozygous mutation in the NRIP1 gene on chromosome 21q11-q21."
    },
    "synonyms": [
        {
            "id": "DOID:0051078",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0051078",
            "name": "congenital anomalies of kidney and urinary tract 3",
            "description": ""
        },
        {
            "id": "MONDO:0032646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032646",
            "name": "congenital anomalies of kidney and urinary tract 3",
            "description": ""
        },
        {
            "id": "MONDO:0032646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032646",
            "name": "CAKUT3",
            "description": ""
        },
        {
            "id": "MIM:618270",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618270",
            "name": "Congenital anomalies of kidney and urinary tract 3",
            "description": "Congenital anomalies of kidney and urinary tract 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051078"
    ],
    "unlinked_id_list": []
}