{
    "disease_id": "DOID:0060895", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "autosomal dominant Parkinson disease 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "autosomal dominant Parkinson's disease 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "autosomal dominant Lewy body Parkinson disease 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "Parkinson disease 4, autosomal dominant; PARK4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "autosomal dominant Parkinson disease type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "PARK4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "Parkinson disease 4, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011562", 
            "name": "Parkinson disease 4, autosomal dominant Lewy body"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060895", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060895", 
            "name": "autosomal dominant Lewy body Parkinson disease 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060895", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060895", 
            "name": "autosomal dominant Parkinson disease 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060895", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060895", 
            "name": "autosomal dominant Parkinson's disease 4"
        }, 
        {
            "url": "https://www.omim.org/entry/605543", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:605543", 
            "name": "Parkinson disease 4, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060895", 
        "description": "A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060895", 
        "name": "Parkinson's disease 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/605543", 
            "id": "605543", 
            "database": "MIM"
        }
    ]
}