{
    "disease_id": "DOID:0060367", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "autosomal dominant Parkinson disease 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "autosomal dominant Parkinson disease type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "Parkinson disease 1, autosomal dominant Lewy body"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "atypical Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "Parkinson disease 1, autosomal dominant; PARK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "autosomal dominant Parkinson's disease 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "Parkinson disease 1, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008200", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008200", 
            "name": "PARK1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060367", 
            "name": "autosomal dominant Parkinson disease 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060367", 
            "name": "autosomal dominant Parkinson's disease 1"
        }, 
        {
            "url": "https://www.omim.org/entry/168601", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:168601", 
            "name": "Parkinson disease 1, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060367", 
        "description": "A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060367", 
        "name": "Parkinson's disease 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/168601", 
            "id": "168601", 
            "database": "MIM"
        }
    ]
}