{
    "disease_id": "DOID:0110573",
    "recommended_name": {
        "id": "DOID:0110573",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110573",
        "name": "autosomal dominant nonsyndromic deafness 4A",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33."
    },
    "synonyms": [
        {
            "id": "DOID:0110573",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110573",
            "name": "DFNA4A",
            "description": ""
        },
        {
            "id": "DOID:0110573",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110573",
            "name": "autosomal dominant deafness 4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "autosomal dominant nonsyndromic hearing loss 4A",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene."
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "DFNA4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "MYH14 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "autosomal dominant deafness 4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "autosomal dominant nonsyndromic deafness 4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in MYH14",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "autosomal dominant nonsyndromic deafness type 4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "deafness, autosomal dominant 4",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "deafness, autosomal dominant 4A",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "deafness, autosomal dominant 4a",
            "description": ""
        },
        {
            "id": "MONDO:0010915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010915",
            "name": "deafness, autosomal dominant type 4A",
            "description": ""
        },
        {
            "id": "MIM:600652",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600652",
            "name": "Deafness, autosomal dominant, 4A",
            "description": "Deafness, autosomal dominant, 4A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110573"
    ],
    "unlinked_id_list": []
}