{
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
            "resource": "Disease Ontology", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "cortical hyperostosis with hyperphosphatemia"
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        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "hypercalcemic tumoral calcinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "hyperostosis with hyperphosphatemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "hyperphosphatemia hyperostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "hyperphosphatemia hyperostosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "hyperphosphatemia tumoral calcinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "lipocalcinogranulomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "morbus Teutschlaender"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "primary hyperphosphatemic tumoral calcinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111063", 
            "name": "tumoral calcinosis with hyperphosphatemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111063", 
        "description": "A calcinosis characterized by autosomal recessive inheritance of elevated blood calcium levels and calcium phosphate crystals in cutaneous and subcutaneous tissues that has_material_basis_in mutation in the GALNT3 gene, the FGF23 gene, or the KL gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111063", 
        "name": "hyperphosphatemic familial tumoral calcinosis"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=2591", 
            "id": "2591", 
            "database": "GlyCosmos"
        }
    ]
}