{
    "disease_id": "DOID:0110584",
    "recommended_name": {
        "id": "DOID:0110584",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110584",
        "name": "autosomal dominant nonsyndromic deafness 6",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "DFNA14",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "DFNA38",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "DFNA6",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "autosomal dominant deafness 14",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "autosomal dominant deafness 38",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "autosomal dominant deafness 6",
            "description": ""
        },
        {
            "id": "DOID:0110584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110584",
            "name": "DFNA6/14/38",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant nonsyndromic hearing loss 6",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the WFS1 gene."
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "DFNA14",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "DFNA38",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "DFNA6",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "WFS1 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant deafness 14",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant deafness 38",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant deafness 6",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant nonsyndromic deafness 6",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in WFS1",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "autosomal dominant nonsyndromic deafness type 6",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "deafness, autosomal dominant 14",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "deafness, autosomal dominant 38",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "deafness, autosomal dominant 6",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "deafness, autosomal dominant 6/14/38",
            "description": ""
        },
        {
            "id": "MONDO:0010963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010963",
            "name": "deafness, autosomal dominant type 6",
            "description": ""
        },
        {
            "id": "MIM:600965",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600965",
            "name": "Deafness, autosomal dominant, 6",
            "description": "Deafness, autosomal dominant, 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110584"
    ],
    "unlinked_id_list": []
}