{
    "disease_id": "DOID:0080383", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "nephrotic syndrome, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "nephrotic syndrome caused by mutation in WT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "diffuse isolated mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "mesangial sclerosis, diffuse"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "nephrotic syndrome, early onset with diffuse mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "WT1 nephrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "diffuse mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "familial mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "DMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "congenital nephrotic syndrome - diffuse mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "nephrotic syndrome, type 4; NPHS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "isolated diffuse mesangial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009733", 
            "name": "NPHS4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080383", 
        "description": "A familial nephrotic syndrome that has_material_basis_in heterozygous mutation in the WT1 gene on chromosome 11p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080383", 
        "name": "nephrotic syndrome type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080383#disease-associations", 
            "id": "0080383", 
            "database": "Alliance of Genome Resources"
        }
    ]
}