{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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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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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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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", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110938", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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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": "", 
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        }, 
        {
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            "description": "", 
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        }
    ], 
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        "url": "http://disease-ontology.org/term/DOID:0110938", 
        "description": "An osteopetrosis characterized by autosomal dominant inheritance of sclerosis predominantly involving the spine, the pelvis, and the skull base, bone fragility and dental abscesses that has_material_basis_in mutation in the CLCN7 gene on chromosome 16p13.", 
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    }, 
    "evidence": [
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        }
    ]
}