{
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            "description": "", 
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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": "", 
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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": "An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in HNRPA2B1 on 7p15.2.", 
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    }, 
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    ]
}