{
    "disease_id": "DOID:0060756", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "sclerosteosis 1; SOST1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "SOST sclerosteosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "SOST"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "sclerosteosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "cortical hyperostosis with syndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "SOST1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010016", 
            "name": "sclerosteosis caused by mutation in SOST"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060756", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060756", 
            "name": "SOST1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060756", 
        "description": "A sclerosteosis that has_material_basis_in homozygous mutation in the SOST gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060756", 
        "name": "sclerosteosis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/269500", 
            "id": "269500", 
            "database": "MIM"
        }
    ]
}