{
    "disease_id": "DOID:0110826",
    "recommended_name": {
        "id": "DOID:0110826",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110826",
        "name": "Usher syndrome type 1",
        "description": "An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa."
    },
    "synonyms": [
        {
            "id": "DOID:0110826",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110826",
            "name": "US1",
            "description": ""
        },
        {
            "id": "DOID:0110826",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110826",
            "name": "USH1",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0070655",
            "label": "Usher syndrome type 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110830",
            "label": "Usher syndrome type 1C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110831",
            "label": "Usher syndrome type 1D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110832",
            "label": "Usher syndrome type 1F",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110834",
            "label": "Usher syndrome type 1G",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0110831",
        "DOID:0070655",
        "DOID:0110834",
        "DOID:0110832",
        "DOID:0110830",
        "DOID:0110826"
    ],
    "unlinked_id_list": []
}