{
    "disease_id": "DOID:0080382", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "nephrotic syndrome, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "nephrotic syndrome, early-onset, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "nephrotic syndrome, type 3; NPHS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "NPHS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "nephrotic syndrome caused by mutation in PLCE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012546", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012546", 
            "name": "PLCE1 nephrotic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080382", 
            "name": "early onset nephrotic syndrome type 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080382", 
        "description": "A familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has_material_basis_in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080382", 
        "name": "nephrotic syndrome type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080382#disease-associations", 
            "id": "0080382", 
            "database": "Alliance of Genome Resources"
        }
    ]
}