{
    "disease_id": "DOID:0080379", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "nephrotic syndrome, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "nephrotic syndrome, type 2; NPHS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "NPHS2 nephrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "SRN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "NPHS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "nephrotic syndrome caused by mutation in NPHS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "nephrotic syndrome, steroid-resistant, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010974", 
            "name": "nephrotic syndrome, idiopathic, steroid-resistant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080379", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080379", 
            "name": "steroid-resistant autosomal recessive nephrotic syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080379", 
        "description": "A familial nephrotic syndrome characterized by steroid resistance and childhood onset of proteinuria, hypoalbuminemia, hyperlipidemia, and edema that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS2 gene encoding podocin on chromosome 1q25-q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080379", 
        "name": "nephrotic syndrome type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080379#disease-associations", 
            "id": "0080379", 
            "database": "Alliance of Genome Resources"
        }
    ]
}