{
    "disease_id": "DOID:0110830",
    "recommended_name": {
        "id": "DOID:0110830",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110830",
        "name": "Usher syndrome type 1C",
        "description": "An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15."
    },
    "synonyms": [
        {
            "id": "DOID:0110830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110830",
            "name": "USH1C",
            "description": ""
        },
        {
            "id": "DOID:0110830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110830",
            "name": "Usher syndrome type I Acadian variety",
            "description": ""
        },
        {
            "id": "DOID:0110830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110830",
            "name": "Usher syndrome type IC",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome type 1C",
            "description": "A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding harmonin on chromosome 11p15. It is inherited in an autosomal recessive manner."
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "USH1C",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome type I Acadian variety",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome type IC",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "USHER syndrome, type IC",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome, Acadian variety",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome, type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010171",
            "name": "Usher syndrome, type I, Acadian variety",
            "description": ""
        },
        {
            "id": "MIM:276904",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/276904",
            "name": "Usher syndrome 1C",
            "description": "Usher syndrome 1C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110830"
    ],
    "unlinked_id_list": []
}