{
    "disease_id": "DOID:0070357",
    "recommended_name": {
        "id": "DOID:0070357",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070357",
        "name": "nephrotic syndrome type 20",
        "description": "A familial nephrotic syndrome that has_material_basis_in X-linked renal disorder characterized by onset of steroid-resistant nephrotic syndrome and proteinuria in the first years of life in affected males."
    },
    "synonyms": [
        {
            "id": "MONDO:0026726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026726",
            "name": "nephrotic syndrome, type 20",
            "description": ""
        },
        {
            "id": "MONDO:0026726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026726",
            "name": "NPHS20",
            "description": ""
        },
        {
            "id": "MIM:301028",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301028",
            "name": "Nephrotic syndrome 20",
            "description": "Nephrotic syndrome 20"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070357"
    ],
    "unlinked_id_list": []
}