{
    "disease_id": "DOID:0110832",
    "recommended_name": {
        "id": "DOID:0110832",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110832",
        "name": "Usher syndrome type 1F",
        "description": "An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q."
    },
    "synonyms": [
        {
            "id": "DOID:0110832",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110832",
            "name": "USH1F",
            "description": ""
        },
        {
            "id": "DOID:0110832",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110832",
            "name": "Usher syndrome type IF",
            "description": ""
        },
        {
            "id": "MONDO:0011186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011186",
            "name": "Usher syndrome type 1F",
            "description": "A form of Usher syndrome type IF that can be caused by homozygous or compound heterozygous mutation in the protocadherin-15 gene (PCDH15) on chromosome 10q. It is inherited in an autosomal recessive manner."
        },
        {
            "id": "MONDO:0011186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011186",
            "name": "USH1F",
            "description": ""
        },
        {
            "id": "MONDO:0011186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011186",
            "name": "Usher syndrome type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011186",
            "name": "USHER syndrome, type IF",
            "description": ""
        },
        {
            "id": "MONDO:0011186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011186",
            "name": "Usher syndrome, type 1F",
            "description": ""
        },
        {
            "id": "MIM:602083",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602083",
            "name": "Usher syndrome 1F",
            "description": "Usher syndrome 1F"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110832"
    ],
    "unlinked_id_list": []
}