{
    "disease_id": "DOID:0070272",
    "recommended_name": {
        "id": "DOID:0070272",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070272",
        "name": "hereditary nonpolyposis colorectal cancer type 5",
        "description": "A Lynch syndrome that has_material_basis_in heterozygous mutation in the MSH6 gene on chromosome 2p16."
    },
    "synonyms": [
        {
            "id": "DOID:0070272",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070272",
            "name": "HNPCC5",
            "description": ""
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "Lynch syndrome 5",
            "description": "An autosomal dominant hereditary neoplastic syndrome caused by pathogenic variants in the MSH6 mismatch repair gene. It is characterized by an increased risk of colorectal cancer in the absence of extensive polyposis, endometrial, ovarian, gastric, small intestinal, and urinary tract cancers, often occuring at younger ages."
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "MSH6 hereditary nonpolyposis colon cancer",
            "description": ""
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "MSH6-related Lynch Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "colorectal cancer, hereditary nonpolyposis, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "hereditary nonpolyposis colon cancer caused by mutation in MSH6",
            "description": ""
        },
        {
            "id": "MONDO:0013710",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013710",
            "name": "HNPCC5",
            "description": ""
        },
        {
            "id": "MIM:614350",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614350",
            "name": "Lynch syndrome 5",
            "description": "Lynch syndrome 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070272"
    ],
    "unlinked_id_list": []
}