{
    "disease_id": "DOID:0060556",
    "recommended_name": {
        "id": "DOID:0060556",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060556",
        "name": "Kufor-Rakeb syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060556",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060556",
            "name": "autosomal recessive Parkinson disease 9",
            "description": ""
        },
        {
            "id": "DOID:0060556",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060556",
            "name": "autosomal recessive juvenile onset Parkinson disease 9",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "Kufor-Rakeb syndrome",
            "description": "Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment."
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "Kufor Rakeb Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "Kufor-Rakeb syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "PARK9",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "KRPPD",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "KRS",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "Parkinson disease type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011706",
            "name": "park 9",
            "description": ""
        },
        {
            "id": "MIM:606693",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606693",
            "name": "Kufor-Rakeb syndrome",
            "description": "Kufor-Rakeb syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060556"
    ],
    "unlinked_id_list": []
}