{
    "disease_id": "DOID:0060371", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "autosomal dominant Parkinson disease 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "autosomal dominant Parkinson's disease 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "Parkinson disease 8, autosomal dominant; PARK8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "Parkinson disease 8, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "PARK8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "autosomal dominant Parkinson disease type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "LRRK2 Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011764", 
            "name": "Parkinson disease caused by mutation in LRRK2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060371", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060371", 
            "name": "autosomal dominant Parkinson disease 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060371", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060371", 
            "name": "autosomal dominant Parkinson's disease 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060371", 
        "description": "A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060371", 
        "name": "Parkinson's disease 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060371#disease-associations", 
            "id": "0060371", 
            "database": "Alliance of Genome Resources"
        }
    ]
}