{
    "disease_id": "DOID:0060895",
    "recommended_name": {
        "id": "DOID:0060895",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060895",
        "name": "Parkinson's disease 4",
        "description": "A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060895",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060895",
            "name": "autosomal dominant Lewy body Parkinson disease 4",
            "description": ""
        },
        {
            "id": "DOID:0060895",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060895",
            "name": "autosomal dominant Parkinson disease 4",
            "description": ""
        },
        {
            "id": "DOID:0060895",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060895",
            "name": "autosomal dominant Parkinson's disease 4",
            "description": ""
        },
        {
            "id": "MONDO:0011562",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011562",
            "name": "autosomal dominant Parkinson disease 4",
            "description": "A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22."
        },
        {
            "id": "MONDO:0011562",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011562",
            "name": "autosomal dominant Parkinson disease 4",
            "description": ""
        },
        {
            "id": "MONDO:0011562",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011562",
            "name": "autosomal dominant Parkinson disease type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011562",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011562",
            "name": "PARK4",
            "description": ""
        },
        {
            "id": "MONDO:0011562",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011562",
            "name": "Parkinson disease 4, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:605543",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605543",
            "name": "Parkinson disease 4, autosomal dominant",
            "description": "Parkinson disease 4, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060895"
    ],
    "unlinked_id_list": []
}