{
    "disease_id": "DOID:0110550",
    "recommended_name": {
        "id": "DOID:0110550",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110550",
        "name": "autosomal dominant nonsyndromic deafness 20",
        "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 ACTG1 gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110550",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110550",
            "name": "DFNA20",
            "description": ""
        },
        {
            "id": "DOID:0110550",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110550",
            "name": "DFNA26",
            "description": ""
        },
        {
            "id": "DOID:0110550",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110550",
            "name": "autosomal dominant deafness 20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "autosomal dominant nonsyndromic hearing loss 20",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene."
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "ACTG1 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "DFNA20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "DFNA26",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "autosomal dominant deafness 20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "autosomal dominant nonsyndromic deafness 20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in ACTG1",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "autosomal dominant nonsyndromic deafness type 20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "deafness, autosomal dominant 20",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "deafness, autosomal dominant 20/26",
            "description": ""
        },
        {
            "id": "MONDO:0011480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011480",
            "name": "deafness, autosomal dominant type 20",
            "description": ""
        },
        {
            "id": "MIM:604717",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604717",
            "name": "Deafness, autosomal dominant, 20",
            "description": "Deafness, autosomal dominant, 20"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110550"
    ],
    "unlinked_id_list": []
}