{
    "disease_id": "DOID:0111130", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "focal segmental glomerulosclerosis caused by mutation in INF2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "focal segmental glomerulosclerosis 5; FSGS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "glomerulosclerosis, focal segmental, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "focal segmental glomerulosclerosis type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "INF2 focal segmental glomerulosclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013191", 
            "name": "FSGS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111130", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111130", 
            "name": "FSGS5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111130", 
        "description": "A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of INF2 on chromosome 14q32.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111130", 
        "name": "focal segmental glomerulosclerosis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613237", 
            "id": "613237", 
            "database": "MIM"
        }
    ]
}