{
    "disease_id": "DOID:0060369", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "autosomal recessive early-onset Parkinson disease 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease 6, autosomal recessive early-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "early-onset Parkinson disease 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "PINK1 Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease, autosomal recessive early-onset, digenic, Pink1/Dj1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease 6, autosomal recessive early-onset; PARK6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease 6, late-onset, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "PARK6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease caused by mutation in PINK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "autosomal recessive early-onset Parkinson disease type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "autosomal recessive early-onset Parkinson's disease 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011613", 
            "name": "Parkinson disease 6, early-onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060369", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060369", 
            "name": "autosomal recessive early-onset Parkinson's disease 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060369", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060369", 
            "name": "early-onset Parkinson disease 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060369", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060369", 
            "name": "autosomal recessive early-onset Parkinson disease 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060369", 
        "description": "An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060369", 
        "name": "Parkinson's disease 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060369#disease-associations", 
            "id": "0060369", 
            "database": "Alliance of Genome Resources"
        }
    ]
}