{
    "disease_id": "DOID:0110546",
    "recommended_name": {
        "id": "DOID:0110546",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110546",
        "name": "autosomal dominant nonsyndromic deafness 15",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110546",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110546",
            "name": "DFNA15",
            "description": ""
        },
        {
            "id": "DOID:0110546",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110546",
            "name": "DFNA52",
            "description": ""
        },
        {
            "id": "DOID:0110546",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110546",
            "name": "autosomal dominant deafness 15",
            "description": ""
        },
        {
            "id": "DOID:0110546",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110546",
            "name": "autosomal dominant deafness 52",
            "description": ""
        },
        {
            "id": "DOID:0110546",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110546",
            "name": "autosomal dominant nonsyndromic deafness 52",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "autosomal dominant nonsyndromic hearing loss 15",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the POU4F3 gene."
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "DFNA15",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "POU4F3 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "autosomal dominant deafness 15",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "autosomal dominant nonsyndromic deafness 15",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in POU4F3",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "autosomal dominant nonsyndromic deafness type 15",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "deafness, autosomal dominant 15",
            "description": ""
        },
        {
            "id": "MONDO:0011226",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011226",
            "name": "deafness, autosomal dominant type 15",
            "description": ""
        },
        {
            "id": "MIM:602459",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602459",
            "name": "Deafness, autosomal dominant, 15",
            "description": "Deafness, autosomal dominant, 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110546"
    ],
    "unlinked_id_list": []
}