{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111405", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111405", 
            "name": "FRASRS1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111405", 
        "description": "A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in FRAS1 on chromosome 4q21.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111405", 
        "name": "Fraser syndrome 1"
    }
}