{
    "disease_id": "DOID:0070608",
    "recommended_name": {
        "id": "DOID:0070608",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070608",
        "name": "autosomal dominant nonsyndromic deafness 81",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ELMOD3 gene on chromosome 2p11."
    },
    "synonyms": [
        {
            "id": "DOID:0070608",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070608",
            "name": "DFNA81",
            "description": ""
        },
        {
            "id": "DOID:0070608",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070608",
            "name": "autosomal dominant deafness 81",
            "description": ""
        },
        {
            "id": "MONDO:0030549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030549",
            "name": "hearing loss, autosomal dominant 81",
            "description": ""
        },
        {
            "id": "MONDO:0030549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030549",
            "name": "DFNA81",
            "description": ""
        },
        {
            "id": "MONDO:0030549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030549",
            "name": "hearing loss, autosomal dominant 81",
            "description": ""
        },
        {
            "id": "MONDO:0030549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030549",
            "name": "deafness, autosomal dominant 81",
            "description": ""
        },
        {
            "id": "MIM:619500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619500",
            "name": "Deafness, autosomal dominant, 81",
            "description": "Deafness, autosomal dominant, 81"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070608"
    ],
    "unlinked_id_list": []
}