{
    "disease_id": "DOID:0060369",
    "recommended_name": {
        "id": "DOID:0060369",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060369",
        "name": "Parkinson's disease 6",
        "description": "An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12."
    },
    "synonyms": [
        {
            "id": "DOID:0060369",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060369",
            "name": "autosomal recessive early-onset Parkinson's disease 6",
            "description": ""
        },
        {
            "id": "DOID:0060369",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060369",
            "name": "early-onset Parkinson disease 6",
            "description": ""
        },
        {
            "id": "DOID:0060369",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060369",
            "name": "autosomal recessive early-onset Parkinson disease 6",
            "description": ""
        },
        {
            "id": "DOID:0060369",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060369",
            "name": "PARK6",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "autosomal recessive early-onset Parkinson disease 6",
            "description": "Any Parkinson disease in which the cause of the disease is a mutation in the PINK1 gene."
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "PINK1 Parkinson disease",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "Parkinson disease caused by mutation in PINK1",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "autosomal recessive early-onset Parkinson disease 6",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "PARK6",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "Parkinson disease 6, autosomal recessive early-onset",
            "description": ""
        },
        {
            "id": "MONDO:0011613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011613",
            "name": "autosomal recessive early-onset Parkinson disease type 6",
            "description": ""
        },
        {
            "id": "MIM:605909",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605909",
            "name": "Parkinson disease 6",
            "description": "Parkinson disease 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060369"
    ],
    "unlinked_id_list": []
}