{
    "disease_id": "DOID:0070274",
    "recommended_name": {
        "id": "DOID:0070274",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070274",
        "name": "hereditary nonpolyposis colorectal cancer type 2",
        "description": "A Lynch syndrome that has_material_basis_in heterozygous mutation in the MLH1 gene on chromosome 3p22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070274",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070274",
            "name": "COCA2",
            "description": ""
        },
        {
            "id": "DOID:0070274",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070274",
            "name": "FCC2",
            "description": ""
        },
        {
            "id": "DOID:0070274",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070274",
            "name": "HNPCC2",
            "description": ""
        },
        {
            "id": "DOID:0070274",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070274",
            "name": "familial nonpolyposis colon cancer type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "Lynch syndrome 2",
            "description": "An autosomal dominant hereditary neoplastic syndrome caused by pathogenic variants in the MLH1 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 occurring at younger ages."
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "Hereditary non-polyposis colon cancer type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "Hereditary nonpolyposis colorectal cancer type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "Lynch 2 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "MLH1-related Lynch syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "colorectal cancer, hereditary nonpolyposis, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "familial non-polyposis colon cancer type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "COCA2",
            "description": ""
        },
        {
            "id": "MONDO:0012249",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012249",
            "name": "HNPCC2",
            "description": ""
        },
        {
            "id": "MIM:609310",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609310",
            "name": "Lynch syndrome 2",
            "description": "Lynch syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070274"
    ],
    "unlinked_id_list": []
}