{
    "disease_id": "DOID:0080673", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013795", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013795", 
            "name": "fibrochondrogenesis 2; FBCG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013795", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013795", 
            "name": "fibrochondrogenesis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013795", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013795", 
            "name": "COL11A2 fibrochondrogenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013795", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013795", 
            "name": "FBCG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013795", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013795", 
            "name": "fibrochondrogenesis caused by mutation in COL11A2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080673", 
        "description": "A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080673", 
        "name": "fibrochondrogenesis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614524", 
            "id": "614524", 
            "database": "MIM"
        }
    ]
}