{
    "disease_id": "DOID:0110590",
    "recommended_name": {
        "id": "DOID:0110590",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110590",
        "name": "autosomal dominant nonsyndromic deafness 69",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110590",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110590",
            "name": "DCUA",
            "description": ""
        },
        {
            "id": "DOID:0110590",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110590",
            "name": "DFNA69",
            "description": ""
        },
        {
            "id": "DOID:0110590",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110590",
            "name": "autosomal dominant deafness 69",
            "description": ""
        },
        {
            "id": "DOID:0110590",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110590",
            "name": "unilateral or asymmetric congenital deafness",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "autosomal dominant nonsyndromic hearing loss 69",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KITLG gene."
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "DCUA",
            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "DFNA69",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "KITLG autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "autosomal dominant deafness 69",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "autosomal dominant nonsyndromic deafness 69",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in KITLG",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "autosomal dominant nonsyndromic deafness type 69",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "deafness, autosomal dominant 69",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "deafness, autosomal dominant 69, unilateral or asymmetric",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "deafness, congenital, unilateral or asymmetric",
            "description": ""
        },
        {
            "id": "MONDO:0014738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014738",
            "name": "unilateral or asymmetric congenital deafness",
            "description": ""
        },
        {
            "id": "MIM:616697",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616697",
            "name": "Deafness, congenital, unilateral or asymmetric",
            "description": "Deafness, congenital, unilateral or asymmetric"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110590"
    ],
    "unlinked_id_list": []
}