{
    "disease_id": "DOID:0070655",
    "recommended_name": {
        "id": "DOID:0070655",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070655",
        "name": "Usher syndrome type 1B",
        "description": "An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070655",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070655",
            "name": "USH1B",
            "description": ""
        },
        {
            "id": "DOID:0070655",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070655",
            "name": "Usher syndrome type IB",
            "description": ""
        },
        {
            "id": "MONDO:0700087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0700087",
            "name": "Usher syndrome type 1B",
            "description": "Usher syndrome in which the cause of the disease is a mutation in the MYO7A gene"
        },
        {
            "id": "MONDO:0700087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0700087",
            "name": "Usher syndrome, type 1B",
            "description": ""
        },
        {
            "id": "MIM:276900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/276900",
            "name": "Usher syndrome 1B",
            "description": "Usher syndrome 1B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070655"
    ],
    "unlinked_id_list": []
}