{
    "disease_id": "DOID:0050576", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "Senior-Loken syndrome 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "SENIOR-Loken syndrome 6; SLSN6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "Senior-Loken syndrome caused by mutation in CEP290"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "SLSN6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "CEP290 Senior-Loken syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012433", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012433", 
            "name": "Senior-Loken syndrome type 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050576", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050576", 
            "name": "Loken Senior syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050576", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050576", 
            "name": "renal-retinal syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050576", 
        "description": "A syndrome characterized by progressive wasting of the filtering unit of the kidney (nephronophthisis), with or without medullary cystic renal disease, and progressive eye disease.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050576", 
        "name": "Senior-Loken syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050576#disease-associations", 
            "id": "0050576", 
            "database": "Alliance of Genome Resources"
        }
    ]
}