{
    "disease_id": "DOID:0110569", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "DFNA44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "autosomal dominant nonsyndromic deafness type 44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "deafness, autosomal dominant 44; DFNA44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "deafness, autosomal dominant 44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "autosomal dominant deafness 44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in CCDC50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "deafness, autosomal dominant type 44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011832", 
            "name": "CCDC50 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110569", 
            "name": "DFNA44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110569", 
            "name": "autosomal dominant deafness 44"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110569", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110569", 
        "name": "autosomal dominant nonsyndromic deafness 44"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110569#disease-associations", 
            "id": "0110569", 
            "database": "Alliance of Genome Resources"
        }
    ]
}