{
    "disease_id": "DOID:0080269", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033260", 
            "name": "deafness, autosomal dominant 73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033260", 
            "name": "DFNA73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033260", 
            "name": "deafness, autosomal dominant 73; DFNA73"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080269", 
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the PTPRQ gene on chromosome 12q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080269", 
        "name": "autosomal dominant nonsyndromic deafness 73"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080269#disease-associations", 
            "id": "0080269", 
            "database": "Alliance of Genome Resources"
        }
    ]
}