{
    "disease_id": "DOID:0110467", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "autosomal recessive deafness 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "autosomal recessive nonsyndromic deafness type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "DFNB12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "deafness, autosomal recessive type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "deafness, autosomal recessive 12; DFNB12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011067", 
            "name": "deafness, autosomal recessive 12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110467", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110467", 
            "name": "DFNB12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110467", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110467", 
            "name": "autosomal recessive deafness 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110467", 
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the CDH23 gene on chromosome 10q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110467", 
        "name": "autosomal recessive nonsyndromic deafness 12"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110467#disease-associations", 
            "id": "0110467", 
            "database": "Alliance of Genome Resources"
        }
    ]
}