{
    "disease_id": "DOID:0070606",
    "recommended_name": {
        "id": "DOID:0070606",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070606",
        "name": "autosomal dominant nonsyndromic deafness 87",
        "description": "An autosomal dominant nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss with inner ear anomalies, including cochlear maldevelopment, absence of the osseous spiral lamina, and/or an enlarged vestibular aqueduct that has_material_basis_in heterozygous mutation in the PI4KB gene on chromosome 1q21."
    },
    "synonyms": [
        {
            "id": "DOID:0070606",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070606",
            "name": "DFNA87",
            "description": ""
        },
        {
            "id": "DOID:0070606",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070606",
            "name": "autosomal dominant deafness 87",
            "description": ""
        },
        {
            "id": "MONDO:0859525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859525",
            "name": "hearing loss, autosomal dominant 87",
            "description": ""
        },
        {
            "id": "MIM:620281",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620281",
            "name": "Deafness, autosomal dominant, 87",
            "description": "Deafness, autosomal dominant, 87"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070606"
    ],
    "unlinked_id_list": []
}