{
    "disease_id": "DOID:0110593",
    "recommended_name": {
        "id": "DOID:0110593",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110593",
        "name": "autosomal dominant nonsyndromic deafness 9",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12."
    },
    "synonyms": [
        {
            "id": "DOID:0110593",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110593",
            "name": "DFNA9",
            "description": ""
        },
        {
            "id": "DOID:0110593",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110593",
            "name": "autosomal dominant deafness 9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "autosomal dominant nonsyndromic deafness 9",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the COCH gene."
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "autosomal dominant nonsyndromic deafness type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "deafness, autosomal dominant type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "deafness, autosomal dominant 9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "DFNA9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "COCH autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in COCH",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "autosomal dominant deafness 9",
            "description": ""
        },
        {
            "id": "MONDO:0011058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011058",
            "name": "deafness, autosomal dominant 9; DFNA9",
            "description": ""
        },
        {
            "id": "MIM:601369",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601369",
            "name": "Deafness, autosomal dominant, 9",
            "description": "Deafness, autosomal dominant, 9"
        }
    ]
}