{
    "disease_id": "DOID:0061193",
    "recommended_name": {
        "id": "DOID:0061193",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061193",
        "name": "nephrotic syndrome type 26",
        "description": "A familial nephrotic syndrome characterized by onset of proteinuria in the first months or years of life that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA5 gene on chromosome 20q13."
    },
    "synonyms": [
        {
            "id": "DOID:0061193",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061193",
            "name": "NPHS26",
            "description": ""
        },
        {
            "id": "MONDO:0031061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031061",
            "name": "nephrotic syndrome, IIa 26",
            "description": ""
        },
        {
            "id": "MONDO:0031061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031061",
            "name": "NPHS26",
            "description": ""
        },
        {
            "id": "MONDO:0031061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031061",
            "name": "nephrotic syndrome, IIa 26",
            "description": ""
        },
        {
            "id": "MIM:620049",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620049",
            "name": "Nephrotic syndrome 26",
            "description": "Nephrotic syndrome 26"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061193"
    ],
    "unlinked_id_list": []
}