{
    "disease_id": "DOID:0110467",
    "recommended_name": {
        "id": "DOID:0110467",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110467",
        "name": "autosomal recessive nonsyndromic deafness 12",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110467",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110467",
            "name": "DFNB12",
            "description": ""
        },
        {
            "id": "DOID:0110467",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110467",
            "name": "autosomal recessive deafness 12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "autosomal recessive nonsyndromic hearing loss 12",
            "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."
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "DFNB12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "autosomal recessive deafness 12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "autosomal recessive nonsyndromic deafness 12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "autosomal recessive nonsyndromic deafness type 12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "deafness, autosomal recessive 12",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "deafness, autosomal recessive 12, modifier of",
            "description": ""
        },
        {
            "id": "MONDO:0011067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011067",
            "name": "deafness, autosomal recessive type 12",
            "description": ""
        },
        {
            "id": "MIM:601386",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601386",
            "name": "Deafness, autosomal recessive, 12",
            "description": "Deafness, autosomal recessive, 12"
        }
    ]
}