{
    "disease_id": "DOID:0110588",
    "recommended_name": {
        "id": "DOID:0110588",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110588",
        "name": "autosomal dominant nonsyndromic deafness 67",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110588",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110588",
            "name": "DFNA67",
            "description": ""
        },
        {
            "id": "DOID:0110588",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110588",
            "name": "autosomal dominant deafness 67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "autosomal dominant nonsyndromic deafness 67",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the OSBPL2 gene."
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "deafness, autosomal dominant 67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "deafness, autosomal dominant 67; DFNA67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "autosomal dominant deafness 67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "autosomal dominant nonsyndromic deafness type 67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "deafness, autosomal dominant type 67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "OSBPL2 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "DFNA67",
            "description": ""
        },
        {
            "id": "MONDO:0014594",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014594",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in OSBPL2",
            "description": ""
        },
        {
            "id": "MIM:616340",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616340",
            "name": "Deafness, autosomal dominant, 67",
            "description": "Deafness, autosomal dominant, 67"
        }
    ]
}