{
    "disease_id": "DOID:0111636",
    "recommended_name": {
        "id": "DOID:0111636",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111636",
        "name": "autosomal recessive nonsyndromic deafness 113",
        "description": "An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in CEACAM16 on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111636",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111636",
            "name": "DFNB113",
            "description": ""
        },
        {
            "id": "DOID:0111636",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111636",
            "name": "autosomal recessive deafness 113",
            "description": ""
        },
        {
            "id": "MIM:618410",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618410",
            "name": "Deafness, autosomal recessive, 113",
            "description": "Deafness, autosomal recessive, 113"
        }
    ]
}