{
    "disease_id": "DOID:0111251", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "Parkinson disease 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "Parkinson disease type 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "DNAJC13 hereditary late onset Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "hereditary late onset Parkinson disease caused by mutation in DNAJC13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "PARK21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014604", 
            "name": "Parkinson disease 21; PARK21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111251", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111251", 
            "name": "PARK21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111251", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111251", 
            "name": "Parkinson disease 21"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111251", 
        "description": "A late onset Parkinson's disease characterized by autosomal dominant inheritance and mean age of onset at 67 years.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111251", 
        "name": "Parkinson's disease 21"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111251#disease-associations", 
            "id": "0111251", 
            "database": "Alliance of Genome Resources"
        }
    ]
}