{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "description": "", 
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "carbonic anhydrase II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110941", 
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            "resource": "Disease Ontology", 
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        {
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            "description": "", 
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        "url": "http://disease-ontology.org/term/DOID:0110941", 
        "description": "An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the CA2 gene on chromosome 8q21.", 
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        "id": "DOID:0110941", 
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    }, 
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        }
    ]
}