{
    "disease_id": "DOID:0080390",
    "recommended_name": {
        "id": "DOID:0080390",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080390",
        "name": "nephrotic syndrome type 1",
        "description": "A familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0080390",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080390",
            "name": "Finnish congenital nephrosis",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "congenital nephrotic syndrome, Finnish type",
            "description": "Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life."
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "Finnish congenital nephrosis",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "congenital nephrotic syndrome - Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "congenital nephrotic syndrome, Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "nephrotic syndrome - NPHS1 associated",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "CnF",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "NPHS1",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "congenital nephrotic syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "congenital nephrotic syndrome Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "nephrosis 1, congenital, Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "nephrosis, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009732",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009732",
            "name": "nephrotic syndrome, type 1",
            "description": ""
        },
        {
            "id": "MIM:256300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256300",
            "name": "Nephrotic syndrome 1",
            "description": "Nephrotic syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080390"
    ],
    "unlinked_id_list": []
}