{
    "disease_id": "DOID:0110493", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012060", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in ESRRB"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal recessive deafness 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012060", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012060", 
            "name": "ESRRB autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012060", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012060", 
            "name": "DFNB35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110493", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110493", 
            "name": "DFNB35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110493", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110493", 
            "name": "autosomal recessive deafness 35"
        }, 
        {
            "url": "https://www.omim.org/entry/608565", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608565", 
            "name": "Deafness, autosomal recessive, 35"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110493", 
        "description": "An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110493", 
        "name": "autosomal recessive nonsyndromic deafness 35"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608565", 
            "id": "608565", 
            "database": "MIM"
        }
    ]
}