{
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            "description": "", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010580", 
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        }, 
        {
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010580", 
            "name": "autoimmune enteropathy type 1"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010580", 
            "name": "Iddm-secretory diarrhea syndrome"
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "enteropathy, autoimmune, with hemolytic Anemia and polyendocrinopathy"
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "resource": "Disease Ontology", 
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            "description": "", 
            "resource": "Disease Ontology", 
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            "description": "", 
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            "description": "", 
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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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            "description": "", 
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        }
    ], 
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        "url": "http://disease-ontology.org/term/DOID:0090110", 
        "description": "An autoimmune hypersensitivity disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
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        "name": "immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome"
    }, 
    "evidence": [
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            "id": "304790", 
            "database": "MIM"
        }
    ]
}