{
    "disease_id": "DOID:0070273", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "colorectal cancer, hereditary nonpolyposis, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "colon cancer, hereditary nonpolyposis, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "colorectal cancer, hereditary nonpolyposis, type 6; HNPCC6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "HNPCC6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "TGFBR2 hereditary nonpolyposis colon cancer"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013695", 
            "name": "hereditary nonpolyposis colon cancer caused by mutation in TGFBR2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070273", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070273", 
            "name": "HNPCC6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070273", 
        "description": "A Lynch syndrome that has_material_basis_in heterozygous mutation in the TGFBR2 gene on chromosome 3p22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070273", 
        "name": "hereditary nonpolyposis colorectal cancer type 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070273#disease-associations", 
            "id": "0070273", 
            "database": "Alliance of Genome Resources"
        }
    ]
}