{
    "disease_id": "DOID:0080386", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014373", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014373", 
            "name": "nephrotic syndrome, type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014373", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014373", 
            "name": "NPHS10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014373", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014373", 
            "name": "EMP2 nephrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014373", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014373", 
            "name": "nephrotic syndrome, type 10; NPHS10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014373", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014373", 
            "name": "nephrotic syndrome caused by mutation in EMP2"
        }, 
        {
            "url": "https://www.omim.org/entry/615861", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615861", 
            "name": "Nephrotic syndrome 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080386", 
        "description": "A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080386", 
        "name": "nephrotic syndrome type 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615861", 
            "id": "615861", 
            "database": "MIM"
        }
    ]
}