{
    "disease_id": "DOID:0110491",
    "recommended_name": {
        "id": "DOID:0110491",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110491",
        "name": "autosomal recessive nonsyndromic deafness 32",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2."
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    "synonyms": [
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            "name": "DFNB32",
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            "url": "https://disease-ontology.org/term/DOID:0110491",
            "name": "autosomal recessive deafness 105",
            "description": ""
        },
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            "name": "autosomal recessive deafness 32",
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        },
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        },
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            "name": "hearing impairment infertile male syndrome",
            "description": ""
        },
        {
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            "name": "autosomal recessive nonsyndromic hearing loss 32",
            "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3."
        },
        {
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            "url": "https://monarchinitiative.org/disease/MONDO:0012091",
            "name": "CDC14A autosomal recessive nonsyndromic deafness",
            "description": ""
        },
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            "description": ""
        },
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        },
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        },
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        },
        {
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            "name": "autosomal recessive nonsyndromic deafness caused by mutation in CDC14A",
            "description": ""
        },
        {
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            "url": "https://monarchinitiative.org/disease/MONDO:0012091",
            "name": "autosomal recessive nonsyndromic deafness type 105",
            "description": ""
        },
        {
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            "name": "autosomal recessive nonsyndromic deafness type 32",
            "description": ""
        },
        {
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            "description": ""
        },
        {
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        },
        {
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            "description": ""
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        {
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            "description": ""
        },
        {
            "id": "MIM:608653",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608653",
            "name": "Deafness, autosomal recessive, 32, with or without immotile sperm",
            "description": "Deafness, autosomal recessive, 32, with or without immotile sperm"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110491"
    ],
    "unlinked_id_list": []
}