{
    "disease_id": "DOID:0081003",
    "recommended_name": {
        "id": "DOID:0081003",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081003",
        "name": "Cowden syndrome 7",
        "description": "A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "Cowden syndrome 7",
            "description": "Any Cowden disease in which the cause of the disease is a mutation in the SEC23B gene."
        },
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "Cowden disease caused by mutation in SEC23B",
            "description": ""
        },
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "Cowden syndrome 7",
            "description": ""
        },
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "Cowden syndrome type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "SEC23B Cowden disease",
            "description": ""
        },
        {
            "id": "MONDO:0014802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014802",
            "name": "CWS7",
            "description": ""
        },
        {
            "id": "MIM:616858",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616858",
            "name": "Cowden syndrome 7",
            "description": "Cowden syndrome 7"
        }
    ]
}