{
    "disease_id": "DOID:0111642",
    "recommended_name": {
        "id": "DOID:0111642",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111642",
        "name": "autosomal recessive nonsyndromic deafness 114",
        "description": "An autosomal recessive nonsyndromic deafness characterized by congenital profound sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in GRAP on chromosome 17p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111642",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111642",
            "name": "DFNB114",
            "description": ""
        },
        {
            "id": "DOID:0111642",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111642",
            "name": "autosomal recessive deafness 114",
            "description": ""
        },
        {
            "id": "MIM:618456",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618456",
            "name": "Deafness, autosomal recessive, 114",
            "description": "Deafness, autosomal recessive, 114"
        }
    ]
}