{
    "disease_id": "DOID:0060371",
    "recommended_name": {
        "id": "DOID:0060371",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060371",
        "name": "Parkinson's disease 8",
        "description": "A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12."
    },
    "synonyms": [
        {
            "id": "DOID:0060371",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060371",
            "name": "autosomal dominant Parkinson disease 8",
            "description": ""
        },
        {
            "id": "DOID:0060371",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060371",
            "name": "autosomal dominant Parkinson's disease 8",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "autosomal dominant Parkinson disease 8",
            "description": "Any Parkinson disease in which the cause of the disease is a mutation in the LRRK2 gene."
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "LRRK2 Parkinson disease",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "Parkinson disease 8",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "Parkinson disease caused by mutation in LRRK2",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "autosomal dominant Parkinson disease 8",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "autosomal dominant Parkinson disease type 8",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "PARK8",
            "description": ""
        },
        {
            "id": "MONDO:0011764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011764",
            "name": "Parkinson disease 8, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:607060",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607060",
            "name": "Parkinson disease 8",
            "description": "Parkinson disease 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060371"
    ],
    "unlinked_id_list": []
}