{
    "disease_id": "DOID:0110984",
    "recommended_name": {
        "id": "DOID:0110984",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110984",
        "name": "Joubert syndrome 15",
        "description": "A Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has_material_basis_in homozygous mutation in the CEP41 gene on chromosome 7q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110984",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110984",
            "name": "JBTS15",
            "description": ""
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "Joubert syndrome 15",
            "description": "Any Joubert syndrome in which the cause of the disease is a mutation in the CEP41 gene."
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "CEP41 Joubert syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "JBTS15",
            "description": ""
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "Joubert syndrome 15",
            "description": ""
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "Joubert syndrome caused by mutation in CEP41",
            "description": ""
        },
        {
            "id": "MONDO:0013763",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013763",
            "name": "Joubert syndrome type 15",
            "description": ""
        },
        {
            "id": "MIM:614464",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614464",
            "name": "Joubert syndrome 15",
            "description": "Joubert syndrome 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110984"
    ],
    "unlinked_id_list": []
}