{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070271", 
            "name": "FCC1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070271", 
            "name": "HNPCC1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070271", 
            "name": "familial nonpolyposis colon cancer type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070271", 
            "name": "hereditary nonpolyposis colorectal cancer type 1"
        }, 
        {
            "url": "https://www.omim.org/entry/120435", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:120435", 
            "name": "Hereditary non-polyposis colorectal cancer 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070271", 
        "description": "A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070271", 
        "name": "Lynch syndrome 1"
    }
}