{
    "disease_id": "DOID:0060556", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Kufor-Rakeb syndrome; KRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "autosomal recessive Parkinson disease 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Parkinson disease 9, autosomal recessive, juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "ceroid lipofuscinosis, neuronal, 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Parkinson disease type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "park 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "KRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "Parkinson disease 9, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "PARK9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "KRPPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011706", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011706", 
            "name": "autosomal recessive juvenile onset Parkinson disease 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060556", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060556", 
            "name": "autosomal recessive Parkinson disease 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060556", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060556", 
            "name": "autosomal recessive juvenile onset Parkinson disease 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060556", 
        "description": "An early-onset Parkinson's disease that is characterized by supranuclear gaze palsy, spasticity, and dementia and has_material_basis_in homozygous or compound heterozygous mutation in a lysosomal type 5 ATPase encoding gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060556", 
        "name": "Kufor-Rakeb syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060556#disease-associations", 
            "id": "0060556", 
            "database": "Alliance of Genome Resources"
        }
    ]
}