{
    "disease_id": "DOID:0080390", 
    "synonyms": [
        {
            "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": "congenital nephrotic syndrome Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009732", 
            "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", 
            "name": "NPHS1"
        }, 
        {
            "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:0080390", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080390", 
            "name": "Finnish congenital nephrosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080390", 
        "description": "A familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080390", 
        "name": "nephrotic syndrome type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080390#disease-associations", 
            "id": "0080390", 
            "database": "Alliance of Genome Resources"
        }
    ]
}