{
    "disease_id": "DOID:0061120",
    "recommended_name": {
        "id": "DOID:0061120",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061120",
        "name": "autosomal dominant tubulointerstitial kidney disease 5",
        "description": "An autosomal dominant tubulointerstitial kidney disease characterized by the onset of progressive chronic renal disease in the first decades of life that has_material_basis_in heterozygous mutation in the SEC61A1 gene on chromosome 3q21."
    },
    "synonyms": [
        {
            "id": "DOID:0061120",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061120",
            "name": "familial juvenile hyperuricemic nephropathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "hyperuricemic nephropathy, familial juvenile type 4",
            "description": "Any familial juvenile hyperuricemic nephropathy in which the cause of the disease is a mutation in the SEC61A1 gene."
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "ADTKD-SEC61A1",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "HNFJ4",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "SEC61A1 familial juvenile hyperuricemic nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "SEC61A1-related autosomal dominant tubulointerstitial kidney disease",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "familial juvenile hyperuricemic nephropathy caused by mutation in SEC61A1",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "hyperuricemic nephropathy, familial juvenile, 4",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "hyperuricemic nephropathy, familial juvenile, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0014891",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014891",
            "name": "tubulointerstitial kidney disease, autosomal dominant, 5",
            "description": ""
        },
        {
            "id": "MIM:617056",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617056",
            "name": "Tubulointerstitial kidney disease, autosomal dominant 5",
            "description": "Tubulointerstitial kidney disease, autosomal dominant 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061120"
    ],
    "unlinked_id_list": []
}