{
    "disease_id": "DOID:0110537",
    "recommended_name": {
        "id": "DOID:0110537",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110537",
        "name": "autosomal recessive nonsyndromic deafness 93",
        "description": "An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CABP2 gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110537",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110537",
            "name": "DFNB93",
            "description": ""
        },
        {
            "id": "DOID:0110537",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110537",
            "name": "autosomal recessive deafness 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive nonsyndromic hearing loss 93",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene."
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive nonsyndromic hearing loss 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "CABP2 autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "DFNB93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive deafness 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive nonsyndromic deafness 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in CABP2",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "autosomal recessive nonsyndromic deafness type 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "deafness, autosomal recessive 93",
            "description": ""
        },
        {
            "id": "MONDO:0013963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013963",
            "name": "deafness, autosomal recessive type 93",
            "description": ""
        },
        {
            "id": "MIM:614899",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614899",
            "name": "Deafness, autosomal recessive, 93",
            "description": "Deafness, autosomal recessive, 93"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110537"
    ],
    "unlinked_id_list": []
}