{
    "disease_id": "DOID:0110491", 
    "synonyms": [
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            "description": "", 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110491", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012091", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012091", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012091", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012091", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://www.omim.org/entry/608653", 
            "description": "Deafness, autosomal recessive, 32, with or without immotile sperm", 
            "resource": "MIM", 
            "id": "MIM:608653", 
            "name": "Deafness, autosomal recessive, 32, with or without immotile sperm"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110491", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110491", 
        "name": "autosomal recessive nonsyndromic deafness 32"
    }
}