{
    "disease_id": "DOID:0060757", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013679", 
            "name": "SOST2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013679", 
            "name": "sclerosteosis 2; SOST2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013679", 
            "name": "sclerosteosis caused by mutation in LRP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013679", 
            "name": "LRP4 sclerosteosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013679", 
            "name": "sclerosteosis type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060757", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060757", 
            "name": "SOST2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060757", 
        "description": "A sclerosteosis that has_material_basis_in heterozygous or homozygous mutation in the LRP4 gene on chromosome 11p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060757", 
        "name": "sclerosteosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614305", 
            "id": "614305", 
            "database": "MIM"
        }
    ]
}