{
    "disease_id": "DOID:0110558",
    "recommended_name": {
        "id": "DOID:0110558",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110558",
        "name": "autosomal dominant nonsyndromic deafness 2A",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2."
    },
    "synonyms": [
        {
            "id": "DOID:0110558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110558",
            "name": "DFNA2A",
            "description": ""
        },
        {
            "id": "DOID:0110558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110558",
            "name": "autosomal dominant deafness 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "autosomal dominant nonsyndromic hearing loss 2A",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KCNQ4 gene."
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "DFNA2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "KCNQ4 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "autosomal dominant deafness 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "autosomal dominant nonsyndromic deafness 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in KCNQ4",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "autosomal dominant nonsyndromic deafness type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "deafness, autosomal dominant 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "deafness, autosomal dominant 2a",
            "description": ""
        },
        {
            "id": "MONDO:0010817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010817",
            "name": "deafness, autosomal dominant type 2A",
            "description": ""
        },
        {
            "id": "MIM:600101",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600101",
            "name": "Deafness, autosomal dominant, 2A",
            "description": "Deafness, autosomal dominant, 2A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110558"
    ],
    "unlinked_id_list": []
}