{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007793", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007793", 
            "name": "HCH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007793", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007793", 
            "name": "hypochondroplasia; HCH"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080041", 
        "description": "An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080041", 
        "name": "hypochondroplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/146000", 
            "id": "146000", 
            "database": "MIM"
        }
    ]
}