{
    "disease_id": "DOID:0060062",
    "recommended_name": {
        "id": "DOID:0060062",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060062",
        "name": "familial juvenile hyperuricemic nephropathy",
        "description": "A kidney disease that is characterized by hyperuricemia with renal uric acid under-excretion, gout and chronic kidney disease."
    },
    "synonyms": [
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "familial juvenile hyperuricemic nephropathy type 1",
            "description": "Familial juvenile hyperuricemic nephropathy type 1 (FJHN1) is a rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age."
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "hyperuricemic nephropathy, familial juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "hyperuricemic nephropathy, familial juvenile, 1; HNFJ1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "familial juvenile hyperuricemic nephropathy caused by mutation in UMOD",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "uromodulin-associated kidney disease",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "UMOD-associated FJHN",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "hyperuricemic nephropathy, familial juvenile, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "UMOD familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "UMOD-associated familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "UMOD-related kidney disease",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "FJHN type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "uromodulin storage disease",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "familial juvenile gouty nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "familial nephropathy with gout",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "hyperuricemic nephropathy, familial juvenile, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "hyperuricemic nephropathy, familial juvenile 1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "nephropathy, familial, with gout",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "HNFJ1",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "familial juvenile hyperuricaemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008073",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008073",
            "name": "gouty nephropathy, familial juvenile",
            "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": "hyperuricemic nephropathy, familial juvenile, 2",
            "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": "hyperuricemic nephropathy, familial juvenile, type 2",
            "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": "early-onset hyperuricemia, Anemia, and progressive kidney failure",
            "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": "hyperuricemic nephropathy, familial juvenile, 2; HNFJ2",
            "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": "REN-associated kidney disease",
            "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": "REN familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0013128",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013128",
            "name": "REN-related autosomal dominant tubulointerstitial kidney disease",
            "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": "ADTKD-REN",
            "description": ""
        },
        {
            "id": "MONDO:0013643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013643",
            "name": "hyperuricemic nephropathy, familial juvenile type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013643",
            "name": "HNFJ3",
            "description": ""
        },
        {
            "id": "MONDO:0013643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013643",
            "name": "hyperuricemic nephropathy, familial juvenile, 3; HNFJ3",
            "description": ""
        },
        {
            "id": "MONDO:0013643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013643",
            "name": "hyperuricemic nephropathy, familial juvenile, 3",
            "description": ""
        },
        {
            "id": "MIM:162000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/162000",
            "name": "Tubulointerstitial kidney disease, autosomal dominant, 1",
            "description": "Tubulointerstitial kidney disease, autosomal dominant, 1"
        },
        {
            "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"
        }
    ]
}