{
    "disease_id": "DOID:0060368",
    "recommended_name": {
        "id": "DOID:0060368",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060368",
        "name": "Parkinson's disease 2",
        "description": "An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27."
    },
    "synonyms": [
        {
            "id": "DOID:0060368",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060368",
            "name": "autosomal recessive juvenile Parkinson disease 2",
            "description": ""
        },
        {
            "id": "DOID:0060368",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060368",
            "name": "autosomal recessive juvenile Parkinson's disease 2",
            "description": ""
        },
        {
            "id": "DOID:0060368",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060368",
            "name": "Parkinson disease juvenile type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "autosomal recessive juvenile Parkinson disease 2",
            "description": "A group of disorders which feature impaired motor control characterized by bradykinesia, muscle rigidity; tremor; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see Parkinson disease), secondary parkinsonism (see Parkinson disease, secondary) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the basal ganglia."
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "PRKN young-onset Parkinson disease",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "Parkinson disease, juvenile, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "autosomal recessive juvenile Parkinson disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "autosomal recessive juvenile Parkinson disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "young-onset Parkinson disease caused by mutation in PRKN",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "JP",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "PARK2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "PDJ",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "Parkinson disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "Parkinson disease 2, autosomal recessive juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "Parkinson disease autosomal recessive, early onset",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "Parkinsonism, early onset, with diurnal fluctuation",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "autosomal recessive juvenile Parkinson disease",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "juvenile parkinsonism",
            "description": ""
        },
        {
            "id": "MIM:600116",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600116",
            "name": "Parkinson disease 2",
            "description": "Parkinson disease 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060368"
    ],
    "unlinked_id_list": []
}