{
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
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            "url": "https://monarchinitiative.org/disease/MONDO:0014179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014179", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111386", 
            "description": "", 
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            "name": "IBMPFD3"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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            "description": "", 
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        }
    ], 
    "recommended_name": {
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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 HNRNPA1 on chromosome 12q13.13.", 
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        }
    ]
}