{
    "disease_id": "DOID:0111758",
    "recommended_name": {
        "id": "DOID:0111758",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111758",
        "name": "Y-linked deafness 2",
        "description": "A Y-linked deafness characterized by male-limited bilateral progressive sensorineural hearing loss of variable severity, with onset in the third to fifth decades of life that has_material_basis_in mutation in the TBL1Y gene on chromosome Yp11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111758",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111758",
            "name": "DFNY2",
            "description": ""
        },
        {
            "id": "MONDO:0027048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027048",
            "name": "deafness, Y-linked 2",
            "description": ""
        },
        {
            "id": "MONDO:0027048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027048",
            "name": "DFNY2",
            "description": ""
        },
        {
            "id": "MONDO:0027048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027048",
            "name": "deafness, Y-linked 2, Y-linked",
            "description": ""
        },
        {
            "id": "MIM:400047",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/400047",
            "name": "Deafness, Y-linked 2",
            "description": "Deafness, Y-linked 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111758"
    ],
    "unlinked_id_list": []
}