{
    "disease_id": "DOID:0060897", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "Parkinson disease 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "Parkinson disease 17; PARK17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "Parkinson disease type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "PARK17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "Parkinson disease caused by mutation in VPS35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "autosomal dominant Parkinson disease 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013625", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013625", 
            "name": "VPS35 Parkinson disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060897", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060897", 
            "name": "Parkinson disease 17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060897", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060897", 
            "name": "autosomal dominant Parkinson disease 17"
        }, 
        {
            "url": "https://www.omim.org/entry/614203", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614203", 
            "name": "Parkinson disease 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060897", 
        "description": "A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060897", 
        "name": "Parkinson's disease 17"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614203", 
            "id": "614203", 
            "database": "MIM"
        }
    ]
}