{
    "disease_id": "DOID:0061119",
    "recommended_name": {
        "id": "DOID:0061119",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061119",
        "name": "autosomal dominant tubulointerstitial kidney disease 4",
        "description": "An autosomal dominant tubulointerstitial kidney disease characterized by early-onset anemia and increased serum uric acid with a bland urinalysis and without proteinuria that has_material_basis_in heterozygous mutation in the renin gene on chromosome 1q32."
    },
    "synonyms": [
        {
            "id": "DOID:0061119",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061119",
            "name": "familial juvenile hyperuricemic nephropathy 2",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "familial juvenile hyperuricemic nephropathy type 2",
            "description": "Familial juvenile hyperuricemic nephropathy type 2 is a rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system (RAS)."
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "ADTKD-REN",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "FJHN type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "REN familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "REN-associated FJHN",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "REN-associated familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "REN-associated kidney disease",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "autosomal dominant tubulointerstitial kidney disease due to mutations in REN",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "familial juvenile hyperuricemic nephropathy caused by mutation in REN",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "familial juvenile hyperuricemic nephropathy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "hyperuricemic nephropathy, familial juvenile, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "tubulointerstitial kidney disease, autosomal dominant, 4",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "HNFJ2",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "hyperuricemic nephropathy, familial juvenile, 2",
            "description": ""
        },
        {
            "id": "MIM:613092",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613092",
            "name": "Tubulointerstitial kidney disease, autosomal dominant 4",
            "description": "Tubulointerstitial kidney disease, autosomal dominant 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061119"
    ],
    "unlinked_id_list": []
}