{
    "disease_id": "DOID:0110545", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "deafness, autosomal dominant 13; DFNA13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "deafness, autosomal dominant 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "COL11A2 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "autosomal dominant nonsyndromic deafness type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in COL11A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "autosomal dominant deafness 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "deafness, autosomal dominant type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011159", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011159", 
            "name": "DFNA13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110545", 
            "name": "DFNA13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110545", 
            "name": "autosomal dominant deafness 13"
        }, 
        {
            "url": "https://www.omim.org/entry/601868", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601868", 
            "name": "Deafness, autosomal dominant, 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110545", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110545", 
        "name": "autosomal dominant nonsyndromic deafness 13"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601868", 
            "id": "601868", 
            "database": "MIM"
        }
    ]
}