{
    "disease_id": "DOID:0111128", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "focal segmental glomerulosclerosis caused by mutation in ACTN4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "glomerulosclerosis, focal segmental, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "focal segmental glomerulosclerosis 1; FSGS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "ACTN4 focal segmental glomerulosclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "FSGS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011303", 
            "name": "focal segmental glomerulosclerosis type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111128", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111128", 
            "name": "FSGS1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111128", 
        "description": "A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of ACTN4 on chromosome 19q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111128", 
        "name": "focal segmental glomerulosclerosis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111128#disease-associations", 
            "id": "0111128", 
            "database": "Alliance of Genome Resources"
        }
    ]
}