{
    "disease_id": "DOID:0110590", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "DCUA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "unilateral or asymmetric congenital deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "KITLG autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "deafness, autosomal dominant 69"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in KITLG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "deafness, autosomal dominant 69; DFNA69"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "deafness, congenital, unilateral or asymmetric"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "autosomal dominant deafness 69"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "DFNA69"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014738", 
            "name": "autosomal dominant nonsyndromic deafness type 69"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110590", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110590", 
            "name": "DCUA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110590", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110590", 
            "name": "DFNA69"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110590", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110590", 
            "name": "autosomal dominant deafness 69"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110590", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110590", 
            "name": "unilateral or asymmetric congenital deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110590", 
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110590", 
        "name": "autosomal dominant nonsyndromic deafness 69"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110590#disease-associations", 
            "id": "0110590", 
            "database": "Alliance of Genome Resources"
        }
    ]
}