{
    "synonyms": [
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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": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014086", 
            "name": "OI, type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014086", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014086", 
            "name": "WNT1 osteogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014086", 
            "name": "osteogenesis imperfecta, type XV; OI15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014086", 
            "name": "OI15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110347", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110347", 
            "name": "OI15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110347", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110347", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615220", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110347", 
        "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the WNT1 gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
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    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615220", 
            "id": "615220", 
            "database": "MIM"
        }
    ]
}
