{
    "disease_id": "DOID:0060370", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "autosomal recessive early-onset Parkinson disease 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "Parkinson disease caused by mutation in PARK7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "PARK7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "autosomal recessive early-onset Parkinson's disease 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "PARK7 Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "autosomal recessive early-onset Parkinson disease type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "Parkinson disease 7, autosomal recessive early-onset; PARK7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011658", 
            "name": "Parkinson disease 7, autosomal recessive early-onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060370", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060370", 
            "name": "autosomal recessive early-onset Parkinson's disease 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060370", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060370", 
            "name": "autosomal recessive early-onset Parkinson disease 7"
        }, 
        {
            "url": "https://www.omim.org/entry/606324", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:606324", 
            "name": "Parkinson disease 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060370", 
        "description": "An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060370", 
        "name": "Parkinson's disease 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/606324", 
            "id": "606324", 
            "database": "MIM"
        }
    ]
}