{
    "disease_id": "DOID:0080381",
    "recommended_name": {
        "id": "DOID:0080381",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080381",
        "name": "nephrotic syndrome type 13",
        "description": "A familial nephrotic syndrome characterized by early onset of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis that has_material_basis_in homozygous mutation in the NUP205 gene on chromosome 7q33."
    },
    "synonyms": [
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "nephrotic syndrome, type 13",
            "description": "Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP205 gene."
        },
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "NPHS13",
            "description": ""
        },
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "NUP205 familial nephrotic syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "familial nephrotic syndrome caused by mutation in NUP205",
            "description": ""
        },
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "nephrotic syndrome, type 13",
            "description": ""
        },
        {
            "id": "MONDO:0014818",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014818",
            "name": "nephrotic syndrome, type 13; NPHS13",
            "description": ""
        },
        {
            "id": "MIM:616893",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616893",
            "name": "Nephrotic syndrome 13",
            "description": "Nephrotic syndrome 13"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080381"
    ],
    "unlinked_id_list": []
}