{
    "disease_id": "DOID:0080037", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "VBCH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "osteosclerosis of the skull and enlarged mandible"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "Worth's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "autosomal dominant osteosclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "Van Buchem disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "Van Buchem disease, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "autosomal dominant endosteal hyperostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011878", 
            "name": "benign form of Worth hyperostosis corticalis generalisata with torus platinus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080037", 
            "name": "autosomal dominant endosteal hyperostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080037", 
            "name": "autosomal dominant osteosclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080037", 
            "name": "benign form of Worth hyperostosis corticalis generalisata with torus platinus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080037", 
            "name": "Worth's syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080037", 
        "description": "A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080037", 
        "name": "Worth syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080037#disease-associations", 
            "id": "0080037", 
            "database": "Alliance of Genome Resources"
        }
    ]
}