{
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            "description": "", 
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        }, 
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        }, 
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        }, 
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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": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014855", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070072", 
            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
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        }
    ], 
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        "url": "http://disease-ontology.org/term/DOID:0070072", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GNB1 on chromosome 1p36.33.", 
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    }, 
    "evidence": [
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            "database": "MIM"
        }
    ]
}