{
    "disease_id": "DOID:1856", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "Cherubism is a rare, self-limiting, fibro-osseous, genetic disease of childhood and adolescence characterized by varying degrees of progressive bilateral enlargement of the mandible and/or maxilla, with clinical repercussions in severe cases.", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "cherubism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "familial multilocular cystic disease of the jaws"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "Crbm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "cherubism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "familial fibrous dysplasia of the jaws"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007315", 
            "name": "CRBM"
        }, 
        {
            "url": "https://www.omim.org/entry/118400", 
            "description": "Cherubism", 
            "resource": "MIM", 
            "id": "MIM:118400", 
            "name": "Cherubism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1856", 
        "description": "A bone disease characterized by replacement of bone in the jaws with fibrous tissue leding to facial swelling that has_material_basis_in heterozygous mutation in SH3BP2 on chromosome 4p16.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1856", 
        "name": "cherubism"
    }
}