{
    "disease_id": "DOID:0110840",
    "recommended_name": {
        "id": "DOID:0110840",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110840",
        "name": "Usher syndrome type 2D",
        "description": "An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110840",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110840",
            "name": "USH2D",
            "description": ""
        },
        {
            "id": "DOID:0110840",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110840",
            "name": "Usher syndrome type IID",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "Usher syndrome type 2D",
            "description": "Any Usher syndrome in which the cause of the disease is a mutation in the WHRN gene."
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "Usher syndrome type IID",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "USH2D",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "USHER syndrome, type IID",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "Usher syndrome caused by mutation in WHRN",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "WHRN Usher syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "USHER syndrome, type IID; USH2D",
            "description": ""
        },
        {
            "id": "MONDO:0012662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012662",
            "name": "Usher syndrome, type 2D",
            "description": ""
        },
        {
            "id": "MIM:611383",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611383",
            "name": "Usher syndrome 2D",
            "description": "Usher syndrome 2D"
        }
    ]
}