{
    "disease_id": "DOID:0111642", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111642", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111642", 
            "name": "DFNB114"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111642", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111642", 
            "name": "autosomal recessive deafness 114"
        }, 
        {
            "url": "https://www.omim.org/entry/618456", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618456", 
            "name": "Deafness, autosomal recessive, 114"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111642", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111642", 
        "name": "autosomal recessive nonsyndromic deafness 114"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618456", 
            "id": "618456", 
            "database": "MIM"
        }
    ]
}