{
    "synonyms": [
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            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "congenital nephrotic syndrome, Finnish type"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrotic syndrome, type 1; NPHS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrosis 1, congenital, Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "congenital nephrotic syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "Finnish congenital nephrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "CnF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrosis, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "congenital nephrotic syndrome - Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrotic syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrotic syndrome - NPHS1 associated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009732", 
            "name": "nephrotic syndrome, congenital"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2590", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2590", 
            "name": "Congenital nephrotic syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/256300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:256300", 
            "name": "Nephrotic syndrome 1"
        }
    ], 
    "recommended_name": {
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        "description": "A nephrotic syndrome that has_material_basis_in genetic mutations.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2590", 
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    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/256300", 
            "id": "256300", 
            "database": "MIM"
        }
    ]
}