{
    "disease_id": "DOID:0080504",
    "recommended_name": {
        "id": "DOID:0080504",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080504",
        "name": "Parkinson's disease 22",
        "description": "A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0080504",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080504",
            "name": "autosomal dominant Parkinson's disease 22",
            "description": ""
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "Parkinson disease 22, autosomal dominant",
            "description": "Any Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene."
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "CHCHD2 Parkinson disease",
            "description": ""
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "PARK22",
            "description": ""
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "Parkinson disease 22, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "Parkinson disease 22, autosomal dominant; PARK22",
            "description": ""
        },
        {
            "id": "MONDO:0014742",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014742",
            "name": "Parkinson disease caused by mutation in CHCHD2",
            "description": ""
        },
        {
            "id": "MIM:616710",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616710",
            "name": "Parkinson disease 22",
            "description": "Parkinson disease 22"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080504"
    ],
    "unlinked_id_list": []
}