{
    "disease_id": "DOID:0070271", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "Lynch syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "COCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "colorectal cancer, hereditary nonpolyposis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "LYNCH syndrome I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "hereditary nonpolyposis colorectal cancer type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "familial non-polyposis colon cancer type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "Lynch 1 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "colon cancer, familial nonpolyposis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "HNPCC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "Lynch syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007356", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007356", 
            "name": "Hereditary non-polyposis colon cancer type 1"
        }, 
        {
            "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"
        }
    ], 
    "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"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070271#disease-associations", 
            "id": "0070271", 
            "database": "Alliance of Genome Resources"
        }
    ]
}