{
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    "synonyms": [
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            "description": "", 
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            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010987", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010987", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010987", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010987", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010987", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110527", 
            "name": "DFNB10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110527", 
            "name": "DFNB8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110527", 
            "name": "NRSD8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110527", 
            "name": "autosomal recessive deafness 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110527", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110527", 
            "description": "", 
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        }, 
        {
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110527", 
        "description": "An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.", 
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        "id": "DOID:0110527", 
        "name": "autosomal recessive nonsyndromic deafness 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110527#disease-associations", 
            "id": "0110527", 
            "database": "Alliance of Genome Resources"
        }
    ]
}