{
    "disease_id": "DOID:0070271",
    "recommended_name": {
        "id": "DOID:0070271",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070271",
        "name": "Lynch syndrome 1",
        "description": "A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16."
    },
    "synonyms": [
        {
            "id": "DOID:0070271",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070271",
            "name": "FCC1",
            "description": ""
        },
        {
            "id": "DOID:0070271",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070271",
            "name": "HNPCC1",
            "description": ""
        },
        {
            "id": "DOID:0070271",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070271",
            "name": "familial nonpolyposis colon cancer type 1",
            "description": ""
        },
        {
            "id": "DOID:0070271",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070271",
            "name": "hereditary nonpolyposis colorectal cancer type 1",
            "description": ""
        },
        {
            "id": "DOID:0070271",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070271",
            "name": "COCA1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "Lynch syndrome 1",
            "description": "An autosomal dominant hereditary neoplastic syndrome caused by pathogenic variants in the MSH2 mismatch repair gene. It is characterized by an increased risk of colorectal cancer in the absense of extensive polyposis, endometrial, ovarian, gastric, small intestinal, and urinary tract cancers, often occuring at younger ages."
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "HNPCC1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "Hereditary non-polyposis colon cancer type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "Lynch 1 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "Lynch syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "Lynch syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "MSH2-related Lynch syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "familial non-polyposis colon cancer type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "hereditary nonpolyposis colorectal cancer type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007356",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007356",
            "name": "COCA1",
            "description": ""
        },
        {
            "id": "MIM:120435",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/120435",
            "name": "Lynch syndrome 1",
            "description": "Lynch syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070271"
    ],
    "unlinked_id_list": []
}