{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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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": "", 
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        }, 
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            "description": "", 
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            "id": "MONDO:0007791", 
            "name": "hypocalciuric hypercalcemia, acquired"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007791", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060700", 
            "name": "FHH type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060700", 
            "description": "", 
            "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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        }
    ], 
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        "url": "http://disease-ontology.org/term/DOID:0060700", 
        "description": "A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21.", 
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        "id": "DOID:0060700", 
        "name": "familial hypocalciuric hypercalcemia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060700#disease-associations", 
            "id": "0060700", 
            "database": "Alliance of Genome Resources"
        }
    ]
}