{
    "disease_id": "DOID:0110842",
    "recommended_name": {
        "id": "DOID:0110842",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110842",
        "name": "Usher syndrome type 3B",
        "description": "An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110842",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110842",
            "name": "USH3B",
            "description": ""
        },
        {
            "id": "DOID:0110842",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110842",
            "name": "Usher syndrome type IIIB",
            "description": ""
        },
        {
            "id": "MONDO:0013788",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013788",
            "name": "Usher syndrome type 3B",
            "description": "Any Usher syndrome in which the cause of the disease is a mutation in the HARS gene."
        },
        {
            "id": "MONDO:0013788",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013788",
            "name": "HARS Usher syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013788",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013788",
            "name": "USH3B",
            "description": ""
        },
        {
            "id": "MONDO:0013788",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013788",
            "name": "Usher syndrome caused by mutation in HARS",
            "description": ""
        },
        {
            "id": "MONDO:0013788",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013788",
            "name": "USHER syndrome, type IIIB",
            "description": ""
        },
        {
            "id": "MIM:614504",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614504",
            "name": "Usher syndrome 3B",
            "description": "Usher syndrome 3B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110842"
    ],
    "unlinked_id_list": []
}