{
    "disease_id": "DOID:0112266",
    "recommended_name": {
        "id": "DOID:0112266",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112266",
        "name": "nephrotic syndrome type 23",
        "description": "A familial nephrotic syndrome characterized by onset of proteinuria in the first or second decade of life, mesangial hypercellularity, focal segmental glomerulosclerosis, and effacement of podocyte foot processes that has_material_basis_in homozygous or compound heterozygous mutation in the KIRREL1 gene on chromosome 1q23.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112266",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112266",
            "name": "NPHS23",
            "description": ""
        },
        {
            "id": "MONDO:0030962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030962",
            "name": "nephrotic syndrome, type 23",
            "description": ""
        },
        {
            "id": "MONDO:0030962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030962",
            "name": "NPHS23",
            "description": ""
        },
        {
            "id": "MONDO:0030962",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030962",
            "name": "nephrotic syndrome, type 23",
            "description": ""
        },
        {
            "id": "MIM:619201",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619201",
            "name": "Nephrotic syndrome 23",
            "description": "Nephrotic syndrome 23"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112266"
    ],
    "unlinked_id_list": []
}