{
    "disease_id": "DOID:0060891", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "juvenile onset Parkinson disease 19A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease 19A, juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "juvenile onset Parkinson disease type 19A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "PARK19A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "DNAJC6 Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "PARK19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "juvenile onset Parkinson's disease 19A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease 19B, early-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease 19, juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease caused by mutation in DNAJC6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease 19A, juvenile-onset; PARK19A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Parkinson disease 19, juvenile-onset; PARK19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014231", 
            "name": "Park19, formerly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060891", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060891", 
            "name": "juvenile onset Parkinson disease 19A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060891", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060891", 
            "name": "juvenile onset Parkinson's disease 19A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060891", 
        "description": "An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060891", 
        "name": "Parkinson's disease 19A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060891#disease-associations", 
            "id": "0060891", 
            "database": "Alliance of Genome Resources"
        }
    ]
}