{
    "disease_id": "DOID:11949",
    "recommended_name": {
        "id": "DOID:11949",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:11949",
        "name": "Creutzfeldt-Jakob disease",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "CJD",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Creutzfeldt Jacob syndrome",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Creutzfeldt Jakob disease",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Creutzfeldt-Jacob disease",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Jakob-Creutzfeldt disease",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Subacute spongiform encephalopathy",
            "description": ""
        },
        {
            "id": "DOID:11949",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11949",
            "name": "Transmissible virus dementia",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "inherited Creutzfeldt-Jakob disease",
            "description": "Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia."
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease, variant, resistance to",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "hereditary Creutzfeldt Jacob disease",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "inherited CJD",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "CJD",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease, Heidenhain variant",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease, familial",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease, sporadic",
            "description": ""
        },
        {
            "id": "MONDO:0007403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007403",
            "name": "Creutzfeldt-Jakob disease, variant",
            "description": ""
        },
        {
            "id": "MIM:123400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/123400",
            "name": "Creutzfeldt-Jakob disease",
            "description": "Creutzfeldt-Jakob disease"
        }
    ]
}