{
    "disease_id": "DOID:0070612",
    "recommended_name": {
        "id": "DOID:0070612",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070612",
        "name": "autosomal dominant nonsyndromic deafness 89",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ATOH1 gene on chromosome 4q22."
    },
    "synonyms": [
        {
            "id": "DOID:0070612",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070612",
            "name": "DFNA89",
            "description": ""
        },
        {
            "id": "DOID:0070612",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070612",
            "name": "autosomal dominant deafness 89",
            "description": ""
        },
        {
            "id": "MONDO:0859528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859528",
            "name": "hearing loss, autosomal dominant 89",
            "description": ""
        },
        {
            "id": "MIM:620284",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620284",
            "name": "Deafness, autosomal dominant, 89",
            "description": "Deafness, autosomal dominant, 89"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070612"
    ],
    "unlinked_id_list": []
}