{
    "disease_id": "DOID:0110841",
    "recommended_name": {
        "id": "DOID:0110841",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110841",
        "name": "Usher syndrome type 3A",
        "description": "An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110841",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110841",
            "name": "USH3A",
            "description": ""
        },
        {
            "id": "DOID:0110841",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110841",
            "name": "Usher syndrome type IIIA",
            "description": ""
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "Usher syndrome type 3A",
            "description": "Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene."
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "CLRN1 Usher syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "USH3A",
            "description": ""
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "Usher syndrome caused by mutation in CLRN1",
            "description": ""
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "Usher syndrome type 3A",
            "description": ""
        },
        {
            "id": "MONDO:0010170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010170",
            "name": "USHER syndrome, type IIIA",
            "description": ""
        },
        {
            "id": "MIM:276902",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/276902",
            "name": "Usher syndrome 3A",
            "description": "Usher syndrome 3A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110841"
    ],
    "unlinked_id_list": []
}