{
    "disease_id": "DOID:0060896", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "autosomal recessive early-onset Parksinson disease 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "young-onset Parkinson disease caused by mutation in VPS13C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "autosomal recessive early-onset Parkinson's disease 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "VPS13C young-onset Parkinson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "Parkinson disease 23, autosomal recessive early-onset; PARK23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "PARK23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "autosomal recessive early-onset Parksinson disease type 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "autosomal recessive early-onset Parkinson disease 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014796", 
            "name": "Parkinson disease 23, autosomal recessive early-onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060896", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060896", 
            "name": "autosomal recessive early-onset Parkinson's disease 23"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060896", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060896", 
            "name": "autosomal recessive early-onset Parkinson disease 23"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060896", 
        "description": "An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060896", 
        "name": "Parkinson's disease 23"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060896#disease-associations", 
            "id": "0060896", 
            "database": "Alliance of Genome Resources"
        }
    ]
}