{
    "disease_id": "DOID:0060368",
    "recommended_name": {
        "id": "DOID:0060368",
        "resource": "Disease Ontology",
        "url": "http://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": "http://disease-ontology.org/term/DOID:0060368",
            "name": "autosomal recessive juvenile Parkinson disease 2",
            "description": ""
        },
        {
            "id": "DOID:0060368",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060368",
            "name": "autosomal recessive juvenile Parkinson's disease 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": "autosomal recessive juvenile Parkinson disease type 2",
            "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": "JP",
            "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, autosomal recessive juvenile; PARK2",
            "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": "Parkinson disease 2, autosomal recessive juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "juvenile parkinsonism",
            "description": ""
        },
        {
            "id": "MONDO:0010820",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010820",
            "name": "autosomal recessive juvenile Parkinson's disease 2",
            "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, juvenile, autosomal recessive",
            "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": "PRKN young-onset Parkinson disease",
            "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": "Parkinsonism, early-onset, with diurnal fluctuation",
            "description": ""
        },
        {
            "id": "MIM:600116",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600116",
            "name": "Parkinson disease 2",
            "description": "Parkinson disease 2"
        }
    ]
}