{
    "disease_id": "DOID:0081074",
    "recommended_name": {
        "id": "DOID:0081074",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081074",
        "name": "Teebi hypertelorism syndrome 2",
        "description": "A Teebi hypertelorism syndrome that has_material_basis_in mutation in heterozygous mutation in the CDH11 gene on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0030674",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030674",
            "name": "Teebi hypertelorism syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0030674",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030674",
            "name": "TBHS2",
            "description": ""
        },
        {
            "id": "MONDO:0030674",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030674",
            "name": "Teebi hypertelorism syndrome 2",
            "description": ""
        },
        {
            "id": "MIM:619736",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619736",
            "name": "Teebi hypertelorism syndrome 2",
            "description": "Teebi hypertelorism syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081074"
    ],
    "unlinked_id_list": []
}