{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033280", 
            "name": "nephrotic syndrome 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033280", 
            "name": "NPHS16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033280", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033280", 
            "name": "nephrotic syndrome 16; NPHS16"
        }, 
        {
            "url": "https://www.omim.org/entry/617783", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617783", 
            "name": "Nephrotic syndrome 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080272", 
        "description": "A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080272", 
        "name": "nephrotic syndrome type 16"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617783", 
            "id": "617783", 
            "database": "MIM"
        }
    ]
}