{
    "disease_id": "DOID:0050834",
    "recommended_name": {
        "id": "DOID:0050834",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050834",
        "name": "CHARGE syndrome",
        "description": "A syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina."
    },
    "synonyms": [
        {
            "id": "DOID:0050834",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050834",
            "name": "CHARGE association",
            "description": ""
        },
        {
            "id": "MONDO:1010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010178",
            "name": "CHD7-related CHARGE syndrome",
            "description": "A CHARGE syndrome in which the cause of the disease is a variation in the CHD7 gene."
        },
        {
            "id": "MONDO:1010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010178",
            "name": "CHARGE syndrome due to CHD7 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:1010178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010178",
            "name": "CHD7-related CHARGE syndrome",
            "description": ""
        },
        {
            "id": "MIM:214800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/214800",
            "name": "CHARGE syndrome",
            "description": "CHARGE syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050834"
    ],
    "unlinked_id_list": []
}