{
    "disease_id": "DOID:0080277",
    "recommended_name": {
        "id": "DOID:0080277",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080277",
        "name": "Joubert syndrome 31",
        "description": "A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP120 gene on chromosome 5q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0033310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033310",
            "name": "Joubert syndrome 31",
            "description": ""
        },
        {
            "id": "MONDO:0033310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033310",
            "name": "JBTS31",
            "description": ""
        },
        {
            "id": "MONDO:0033310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033310",
            "name": "Joubert syndrome 31; JBTS31",
            "description": ""
        },
        {
            "id": "MIM:617761",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617761",
            "name": "Joubert syndrome 31",
            "description": "Joubert syndrome 31"
        }
    ]
}